ClinVar for Gene (Select 675) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3076204	NM_000059.4(BRCA2):c.8953+6T>C	BRCA2	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3076083	NM_000059.4(BRCA2):c.9508_9510del (p.Asp3170del)	BRCA2 (D1031del +4 more)	Deletion (inframe_deletion +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3076082	NM_000059.4(BRCA2):c.9257-14T>C	BRCA2	Single nucleotide variant (intron variant)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 3076066	NM_000059.4(BRCA2):c.5921dup (p.Cys1975fs)	BRCA2 (C1975fs)	Duplication (frameshift variant +2 more)	Hereditary breast ovarian cancer syndrome	GPathogenic
Select item 3076065	NM_000059.4(BRCA2):c.4555_4556del (p.Pro1519fs)	BRCA2 (P1519fs)	Deletion (frameshift variant +2 more)	Hereditary breast ovarian cancer syndrome	GPathogenic
Select item 3076064	NM_000059.4(BRCA2):c.2488_2489insG (p.Asn830fs)	BRCA2 (N830fs)	Insertion (frameshift variant +2 more)	Hereditary breast ovarian cancer syndrome	GPathogenic
Select item 3076052	NM_000059.4(BRCA2):c.3969_3970insCT (p.Tyr1324fs)	BRCA2 (Y1324fs)	Insertion (frameshift variant +2 more)	Hereditary breast ovarian cancer syndrome	GPathogenic
Select item 3076024	NM_000059.4(BRCA2):c.2556_2557insATCAGATT (p.Gln853fs)	BRCA2 (Q853fs)	Insertion (frameshift variant +2 more)	Hereditary breast ovarian cancer syndrome	GPathogenic
Select item 3076020	NM_000059.4(BRCA2):c.5233dup (p.Met1745fs)	BRCA2 (M1745fs)	Duplication (frameshift variant +2 more)	Hereditary breast ovarian cancer syndrome	GPathogenic
Select item 3075859	NM_000059.4(BRCA2):c.8833C>T (p.Gln2945Ter)	BRCA2 (Q1301* +3 more)	Single nucleotide variant (nonsense +1 more)	Hereditary breast ovarian cancer syndrome	GLikely pathogenic
Select item 3075839	NM_000059.4(BRCA2):c.6592G>A (p.Glu2198Lys)	BRCA2 (E2198K)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3075813	NM_000059.4(BRCA2):c.5569del (p.Glu1857fs)	BRCA2 (E1857fs)	Deletion (frameshift variant)	Hereditary breast ovarian cancer syndrome	GLikely pathogenic
Select item 3075812	NM_000059.4(BRCA2):c.4780_4787del (p.Met1594fs)	BRCA2 (M1594fs)	Deletion (frameshift variant +2 more)	Hereditary breast ovarian cancer syndrome	GLikely pathogenic
Select item 3075796	NM_000059.4(BRCA2):c.2408dup (p.Tyr803Ter)	BRCA2 (Y803*)	Duplication (nonsense +2 more)	Hereditary breast ovarian cancer syndrome	GPathogenic
Select item 3075792	NM_000059.4(BRCA2):c.9399del (p.Gly3134fs)	BRCA2 (G1490fs +4 more)	Deletion (frameshift variant +1 more)	Hereditary breast ovarian cancer syndrome	GLikely pathogenic
Select item 3075791	NM_000059.4(BRCA2):c.9278T>A (p.Leu3093Ter)	BRCA2 (L1449* +4 more)	Single nucleotide variant (nonsense +1 more)	Hereditary breast ovarian cancer syndrome	GLikely pathogenic
Select item 3075790	NM_000059.4(BRCA2):c.7582_7583insA (p.Gly2528fs)	BRCA2 (G2496fs +3 more)	Insertion (frameshift variant +1 more)	Hereditary breast ovarian cancer syndrome	GLikely pathogenic
Select item 3075789	NM_000059.4(BRCA2):c.7577_7580del (p.Ala2526fs)	BRCA2 (A2494fs +3 more)	Deletion (frameshift variant +1 more)	Hereditary breast ovarian cancer syndrome	GLikely pathogenic
Select item 3075788	NM_000059.4(BRCA2):c.6887del (p.Ile2296fs)	BRCA2 (I157fs +2 more)	Deletion (frameshift variant +2 more)	Hereditary breast ovarian cancer syndrome	GLikely pathogenic
Select item 3075787	NM_000059.4(BRCA2):c.5960del (p.Gln1987fs)	BRCA2 (Q1987fs)	Deletion (frameshift variant +2 more)	Hereditary breast ovarian cancer syndrome	GLikely pathogenic
Select item 3075786	NM_000059.4(BRCA2):c.4718_4719del (p.Ala1572_Cys1573insTer)	BRCA2	Deletion (nonsense +2 more)	Hereditary breast ovarian cancer syndrome	GLikely pathogenic
Select item 3075785	NM_000059.4(BRCA2):c.4714_4715insGCAAAGAC (p.Ala1572fs)	BRCA2 (A1572fs)	Insertion (frameshift variant)	Hereditary breast ovarian cancer syndrome	GLikely pathogenic
Select item 3075784	NM_000059.4(BRCA2):c.4464del (p.His1488fs)	BRCA2 (H1488fs)	Deletion (frameshift variant +2 more)	Hereditary breast ovarian cancer syndrome	GLikely pathogenic
Select item 3075783	NM_000059.4(BRCA2):c.4163del (p.Thr1388fs)	BRCA2 (T1388fs)	Deletion (frameshift variant)	Hereditary breast ovarian cancer syndrome	GLikely pathogenic
Select item 3075769	NM_000059.4(BRCA2):c.607_610del (p.Thr203fs)	BRCA2 (T203fs +1 more)	Microsatellite (frameshift variant +1 more)	Hereditary breast ovarian cancer syndrome	GLikely pathogenic
Select item 3075636	NM_000059.4(BRCA2):c.8401_8403del (p.Phe2801del)	BRCA2 (F1157del +3 more)	Deletion (inframe_deletion +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075635	NM_000059.4(BRCA2):c.7210A>G (p.Lys2404Glu)	BRCA2 (K2372E +3 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075634	NM_000059.4(BRCA2):c.6378C>T (p.Cys2126=)	BRCA2	Single nucleotide variant (synonymous variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3075633	NM_000059.4(BRCA2):c.6080G>T (p.Arg2027Ile)	BRCA2 (R2027I)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075632	NM_000059.4(BRCA2):c.5962G>T (p.Val1988Leu)	BRCA2 (V1988L)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075631	NM_000059.4(BRCA2):c.5592C>T (p.Asp1864=)	BRCA2	Single nucleotide variant (synonymous variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3075630	NM_000059.4(BRCA2):c.5558G>T (p.Cys1853Phe)	BRCA2 (C1853F)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075629	NM_000059.4(BRCA2):c.5557T>C (p.Cys1853Arg)	BRCA2 (C1853R)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075628	NM_000059.4(BRCA2):c.4996A>G (p.Asn1666Asp)	BRCA2 (N1666D)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075627	NM_000059.4(BRCA2):c.4344T>C (p.Asn1448=)	BRCA2	Single nucleotide variant (synonymous variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3075625	NM_000059.4(BRCA2):c.3860A>T (p.Asn1287Ile)	BRCA2 (N1287I)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075623	NM_000059.4(BRCA2):c.3726T>C (p.Ser1242=)	BRCA2	Single nucleotide variant (synonymous variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3075622	NM_000059.4(BRCA2):c.2413T>A (p.Ser805Thr)	BRCA2 (S805T)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075621	NM_000059.4(BRCA2):c.2296G>A (p.Ala766Thr)	BRCA2 (A766T)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075620	NM_000059.4(BRCA2):c.1999C>T (p.Leu667=)	BRCA2	Single nucleotide variant (synonymous variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3075619	NM_000059.4(BRCA2):c.1687T>C (p.Trp563Arg)	BRCA2 (W563R)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075618	NM_000059.4(BRCA2):c.1498G>T (p.Gly500Cys)	BRCA2 (G500C)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075453	NM_000059.4(BRCA2):c.2324C>A (p.Ser775Tyr)	BRCA2 (S775Y)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075384	NM_000059.4(BRCA2):c.410_412del (p.Ser137del)	BRCA2 (S137del +1 more)	Deletion (inframe_deletion +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075382	NM_000059.4(BRCA2):c.4152G>C (p.Leu1384Phe)	BRCA2 (L1384F)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075310	NM_000059.4(BRCA2):c.4654G>T (p.Gly1552Cys)	BRCA2 (G1552C)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075180	NM_000059.4(BRCA2):c.3086T>A (p.Met1029Lys)	BRCA2 (M1029K)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075171	NM_000059.4(BRCA2):c.4931A>G (p.Glu1644Gly)	BRCA2 (E1644G)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075159	NM_000059.4(BRCA2):c.9990A>T (p.Glu3330Asp)	BRCA2 (E1191D +4 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075123	NM_000059.4(BRCA2):c.4690G>C (p.Ala1564Pro)	BRCA2 (A1564P)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3075086	NM_000059.4(BRCA2):c.9599C>T (p.Ser3200Leu)	BRCA2 (S1061L +4 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3074768	NM_000059.4(BRCA2):c.9685C>A (p.Pro3229Thr)	BRCA2 (P1090T +4 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3074699	NM_000059.4(BRCA2):c.6387A>G (p.Glu2129=)	BRCA2	Single nucleotide variant (synonymous variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3074413	NM_000059.4(BRCA2):c.10145T>G (p.Leu3382Arg)	BRCA2 (L1243R +4 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3074170	NM_000059.4(BRCA2):c.1350T>C (p.Ser450=)	BRCA2	Single nucleotide variant (synonymous variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3074130	NM_000059.4(BRCA2):c.3644_3646delinsTAAAAAGG (p.Gly1215fs)	BRCA2 (G1215fs)	Indel (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3074016	NM_000059.4(BRCA2):c.7991T>C (p.Ile2664Thr)	BRCA2 (I1020T +3 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3073896	NM_000059.4(BRCA2):c.5812G>A (p.Gly1938Arg)	BRCA2 (G1938R)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3073868	NM_000059.4(BRCA2):c.3419_3421del (p.Ser1140del)	BRCA2 (S1140del)	Deletion (inframe_deletion +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3073847	NM_000059.4(BRCA2):c.337A>G (p.Arg113Gly)	BRCA2 (R113G)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3073799	NM_000059.4(BRCA2):c.9636A>G (p.Gly3212=)	BRCA2	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3073658	NM_000059.4(BRCA2):c.7089T>A (p.Tyr2363Ter)	BRCA2 (Y224* +3 more)	Single nucleotide variant (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3073635	NM_000059.4(BRCA2):c.1068T>G (p.Ser356=)	BRCA2	Single nucleotide variant (synonymous variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3073618	NM_000059.4(BRCA2):c.8072C>A (p.Ser2691Tyr)	BRCA2 (S1047Y +3 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3073591	NM_000059.4(BRCA2):c.9759T>A (p.Cys3253Ter)	BRCA2 (C1114* +4 more)	Single nucleotide variant (nonsense +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely pathogenic
Select item 3073463	NM_000059.4(BRCA2):c.2122T>G (p.Ser708Ala)	BRCA2 (S708A)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3073424	NM_000059.4(BRCA2):c.8340T>G (p.Ala2780=)	BRCA2	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3073334	NM_000059.4(BRCA2):c.8755-15C>G	BRCA2	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3073227	NM_000059.4(BRCA2):c.6427T>A (p.Ser2143Thr)	BRCA2 (S2143T)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3073175	NM_000059.4(BRCA2):c.7186T>G (p.Leu2396Val)	BRCA2 (L2364V +3 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3073087	NM_000059.4(BRCA2):c.9318G>C (p.Trp3106Cys)	BRCA2 (W1462C +4 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3072932	NM_000059.4(BRCA2):c.9532A>G (p.Asn3178Asp)	BRCA2 (N1039D +4 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3072828	NM_000059.4(BRCA2):c.5100_5102del (p.Gln1701del)	BRCA2 (Q1701del)	Deletion (inframe_deletion +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3072782	NM_000059.4(BRCA2):c.2562del (p.Asn854fs)	BRCA2 (N854fs)	Deletion (frameshift variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GPathogenic
Select item 3072760	NM_000059.4(BRCA2):c.2732A>G (p.Glu911Gly)	BRCA2 (E911G)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3072537	NM_000059.4(BRCA2):c.4203T>G (p.Gly1401=)	BRCA2	Single nucleotide variant (synonymous variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3072356	NM_000059.4(BRCA2):c.7942A>C (p.Ser2648Arg)	BRCA2 (S1004R +3 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3072084	NM_000059.4(BRCA2):c.10185del (p.Ser3396fs)	BRCA2 (S1257fs +4 more)	Deletion (frameshift variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3072032	NM_000059.4(BRCA2):c.2305C>G (p.Leu769Val)	BRCA2 (L769V)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3071937	NM_000059.4(BRCA2):c.4410A>G (p.Ile1470Met)	BRCA2 (I1470M)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3071911	NM_000059.4(BRCA2):c.1999C>G (p.Leu667Val)	BRCA2 (L667V)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3071725	NM_000059.4(BRCA2):c.8000G>A (p.Ser2667Asn)	BRCA2 (S1023N +3 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3071721	NM_000059.4(BRCA2):c.10030C>A (p.Leu3344Ile)	BRCA2 (L1205I +4 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3071664	NM_000059.4(BRCA2):c.786A>G (p.Ala262=)	BRCA2	Single nucleotide variant (synonymous variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3071655	NM_000059.4(BRCA2):c.7618-14T>A	BRCA2	Single nucleotide variant (intron variant)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3071574	NM_000059.4(BRCA2):c.10229A>T (p.Asp3410Val)	BRCA2 (D1271V +4 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3071456	NM_000059.4(BRCA2):c.3668A>T (p.His1223Leu)	BRCA2 (H1223L)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3071452	NM_000059.4(BRCA2):c.6687A>T (p.Glu2229Asp)	BRCA2 (E2229D)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3071448	NM_000059.4(BRCA2):c.4460A>C (p.Lys1487Thr)	BRCA2 (K1487T)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3071401	NM_000059.4(BRCA2):c.4015A>C (p.Ser1339Arg)	BRCA2 (S1339R)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3071243	NM_000059.4(BRCA2):c.8846G>A (p.Arg2949Lys)	BRCA2 (R1305K +3 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3070999	NM_000059.4(BRCA2):c.8273T>C (p.Leu2758Pro)	BRCA2 (L1114P +3 more)	Single nucleotide variant (missense variant +1 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3070694	NM_000059.4(BRCA2):c.4633C>A (p.Leu1545Ile)	BRCA2 (L1545I)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3070628	NM_000059.4(BRCA2):c.5263G>A (p.Glu1755Lys)	BRCA2 (E1755K)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3070572	NM_000059.4(BRCA2):c.4322A>T (p.Glu1441Val)	BRCA2 (E1441V)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3070303	NM_000059.4(BRCA2):c.2721G>A (p.Lys907=)	BRCA2	Single nucleotide variant (synonymous variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GLikely benign
Select item 3069577	NM_000059.4(BRCA2):c.3631G>A (p.Glu1211Lys)	BRCA2 (E1211K)	Single nucleotide variant (missense variant +2 more)	Breast-ovarian cancer, familial, susceptibility to, 2	GUncertain significance
Select item 3069005	NM_000059.4(BRCA2):c.9257-19T>G	BRCA2	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3068995	NM_000059.4(BRCA2):c.3096_3100inv (p.Lys1032_Ile1034delinsAsnIlePhe)	BRCA2	Inversion (missense variant +2 more)	not specified	GUncertain significance
Select item 3068901	NM_000059.4(BRCA2):c.3096_3098del (p.Lys1032_Asp1033delinsAsn)	BRCA2	Deletion (inframe_indel +2 more)	not specified	GUncertain significance

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