ClinVar for Gene (Select 57619) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3162000	NM_020859.4(SHROOM3):c.5950A>G (p.Thr1984Ala)	SHROOM3, SHROOM3-AS1 (T1984A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161999	NM_020859.4(SHROOM3):c.5936C>T (p.Pro1979Leu)	SHROOM3, SHROOM3-AS1 (P1979L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161998	NM_020859.4(SHROOM3):c.5675G>A (p.Arg1892Gln)	SHROOM3, SHROOM3-AS1 (R1892Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161997	NM_020859.4(SHROOM3):c.5619A>T (p.Glu1873Asp)	SHROOM3, SHROOM3-AS1 (E1873D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161996	NM_020859.4(SHROOM3):c.5417C>T (p.Thr1806Met)	SHROOM3, SHROOM3-AS1 (T1806M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3161995	NM_020859.4(SHROOM3):c.5186G>A (p.Cys1729Tyr)	SHROOM3, SHROOM3-AS1 (C1729Y)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3161994	NM_020859.4(SHROOM3):c.5111C>A (p.Pro1704His)	SHROOM3, SHROOM3-AS1 (P1704H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3161993	NM_020859.4(SHROOM3):c.5011T>G (p.Leu1671Val)	SHROOM3, SHROOM3-AS1 (L1671V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3161992	NM_020859.4(SHROOM3):c.4468T>C (p.Ser1490Pro)	SHROOM3, SHROOM3-AS1 (S1490P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161991	NM_020859.4(SHROOM3):c.4438A>G (p.Ser1480Gly)	SHROOM3, SHROOM3-AS1 (S1480G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161990	NM_020859.4(SHROOM3):c.4387C>G (p.Leu1463Val)	SHROOM3, SHROOM3-AS1 (L1463V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161988	NM_020859.4(SHROOM3):c.4353T>A (p.Phe1451Leu)	SHROOM3, SHROOM3-AS1 (F1451L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161987	NM_020859.4(SHROOM3):c.4216G>A (p.Asp1406Asn)	SHROOM3, SHROOM3-AS1 (D1406N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3161986	NM_020859.4(SHROOM3):c.401C>A (p.Pro134His)	SHROOM3, SHROOM3-AS1 (P134H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3161985	NM_020859.4(SHROOM3):c.3953G>T (p.Gly1318Val)	SHROOM3, SHROOM3-AS1 (G1318V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161984	NM_020859.4(SHROOM3):c.3361C>T (p.Leu1121Phe)	SHROOM3, SHROOM3-AS1 (L1121F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161983	NM_020859.4(SHROOM3):c.3340G>A (p.Glu1114Lys)	SHROOM3, SHROOM3-AS1 (E1114K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161981	NM_020859.4(SHROOM3):c.3188G>C (p.Arg1063Pro)	SHROOM3, SHROOM3-AS1 (R1063P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161980	NM_020859.4(SHROOM3):c.3136G>A (p.Gly1046Arg)	SHROOM3, SHROOM3-AS1 (G1046R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161979	NM_020859.4(SHROOM3):c.3134A>G (p.Asn1045Ser)	SHROOM3, SHROOM3-AS1 (N1045S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161978	NM_020859.4(SHROOM3):c.3121G>T (p.Gly1041Cys)	SHROOM3, SHROOM3-AS1 (G1041C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161977	NM_020859.4(SHROOM3):c.3004G>A (p.Ala1002Thr)	SHROOM3, SHROOM3-AS1 (A1002T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161976	NM_020859.4(SHROOM3):c.2930C>T (p.Ala977Val)	SHROOM3, SHROOM3-AS1 (A977V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161975	NM_020859.4(SHROOM3):c.2797T>C (p.Ser933Pro)	SHROOM3, SHROOM3-AS1 (S933P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161974	NM_020859.4(SHROOM3):c.2699G>A (p.Arg900Lys)	SHROOM3, SHROOM3-AS1 (R900K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3161973	NM_020859.4(SHROOM3):c.2647G>A (p.Ala883Thr)	SHROOM3, SHROOM3-AS1 (A883T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161972	NM_020859.4(SHROOM3):c.2615C>G (p.Ser872Trp)	SHROOM3, SHROOM3-AS1 (S872W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161971	NM_020859.4(SHROOM3):c.2468A>G (p.Asn823Ser)	SHROOM3, SHROOM3-AS1 (N823S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161970	NM_020859.4(SHROOM3):c.2339C>T (p.Ser780Leu)	SHROOM3, SHROOM3-AS1 (S780L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161969	NM_020859.4(SHROOM3):c.2243C>G (p.Pro748Arg)	SHROOM3, SHROOM3-AS1 (P748R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161967	NM_020859.4(SHROOM3):c.2006C>T (p.Pro669Leu)	SHROOM3, SHROOM3-AS1 (P669L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161966	NM_020859.4(SHROOM3):c.1532T>C (p.Met511Thr)	SHROOM3, SHROOM3-AS1 (M511T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161965	NM_020859.4(SHROOM3):c.1240C>T (p.Arg414Trp)	SHROOM3, SHROOM3-AS1 (R414W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161964	NM_020859.4(SHROOM3):c.11C>A (p.Thr4Asn)	SHROOM3 (T4N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161962	NM_020859.4(SHROOM3):c.1186C>T (p.Arg396Trp)	SHROOM3, SHROOM3-AS1 (R396W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3161961	NM_020859.4(SHROOM3):c.1067T>C (p.Val356Ala)	SHROOM3, SHROOM3-AS1 (V356A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3062778	GRCh37/hg19 4q13.3-21.21(chr4:74822261-79345650)x1	AREG, ART3 +37 more	Copy number loss	not specified	GUncertain significance
Select item 3056806	NM_020859.4(SHROOM3):c.3160G>T (p.Val1054Leu)	SHROOM3, SHROOM3-AS1 (V1054L)	Single nucleotide variant (missense variant)	SHROOM3-related disorder	GBenign
Select item 3055367	NM_020859.4(SHROOM3):c.316G>C (p.Val106Leu)	SHROOM3 (V106L)	Single nucleotide variant (missense variant)	SHROOM3-related disorder	GLikely benign
Select item 3055331	NM_020859.4(SHROOM3):c.2799C>T (p.Ser933=)	SHROOM3, SHROOM3-AS1	Single nucleotide variant (synonymous variant)	SHROOM3-related disorder	GBenign
Select item 3053420	NM_020859.4(SHROOM3):c.1263C>T (p.Gly421=)	SHROOM3, SHROOM3-AS1	Single nucleotide variant (synonymous variant)	SHROOM3-related disorder	GLikely benign
Select item 3052271	NM_020859.4(SHROOM3):c.697C>A (p.Pro233Thr)	SHROOM3, SHROOM3-AS1 (P233T)	Single nucleotide variant (missense variant)	SHROOM3-related disorder	GLikely benign
Select item 3051250	NM_020859.4(SHROOM3):c.3870G>A (p.Pro1290=)	SHROOM3, SHROOM3-AS1	Single nucleotide variant (synonymous variant)	SHROOM3-related disorder	GBenign
Select item 3050398	NM_020859.4(SHROOM3):c.619C>T (p.His207Tyr)	SHROOM3, SHROOM3-AS1 (H207Y)	Single nucleotide variant (missense variant)	SHROOM3-related disorder	GBenign
Select item 3048279	NM_020859.4(SHROOM3):c.1101T>G (p.Ser367Arg)	SHROOM3, SHROOM3-AS1 (S367R)	Single nucleotide variant (missense variant)	SHROOM3-related disorder	GLikely benign
Select item 3046757	NM_020859.4(SHROOM3):c.2103A>G (p.Ala701=)	SHROOM3, SHROOM3-AS1	Single nucleotide variant (synonymous variant)	SHROOM3-related disorder	GLikely benign
Select item 3046035	NM_020859.4(SHROOM3):c.3525C>T (p.Ala1175=)	SHROOM3, SHROOM3-AS1	Single nucleotide variant (synonymous variant)	SHROOM3-related disorder	GLikely benign
Select item 3042762	NM_020859.4(SHROOM3):c.2262C>T (p.Ser754=)	SHROOM3, SHROOM3-AS1	Single nucleotide variant (synonymous variant)	SHROOM3-related disorder	GLikely benign
Select item 3042733	NM_020859.4(SHROOM3):c.4596T>A (p.Pro1532=)	SHROOM3, SHROOM3-AS1	Single nucleotide variant (synonymous variant)	SHROOM3-related disorder	GLikely benign
Select item 3042693	NM_020859.4(SHROOM3):c.2928C>T (p.Ser976=)	SHROOM3, SHROOM3-AS1	Single nucleotide variant (synonymous variant)	SHROOM3-related disorder	GLikely benign
Select item 3041110	NM_020859.4(SHROOM3):c.3393C>T (p.Ser1131=)	SHROOM3, SHROOM3-AS1	Single nucleotide variant (synonymous variant)	SHROOM3-related disorder	GBenign
Select item 3040757	NM_020859.4(SHROOM3):c.4581C>T (p.Pro1527=)	SHROOM3, SHROOM3-AS1	Single nucleotide variant (synonymous variant)	SHROOM3-related disorder	GLikely benign
Select item 3040646	NM_020859.4(SHROOM3):c.-8T>A	SHROOM3	Single nucleotide variant (5 prime UTR variant)	SHROOM3-related disorder	GBenign
Select item 3040550	NM_020859.4(SHROOM3):c.2868C>T (p.Ser956=)	SHROOM3, SHROOM3-AS1	Single nucleotide variant (synonymous variant)	SHROOM3-related disorder	GLikely benign
Select item 3040201	NM_020859.4(SHROOM3):c.4602G>A (p.Pro1534=)	SHROOM3, SHROOM3-AS1	Single nucleotide variant (synonymous variant)	SHROOM3-related disorder	GLikely benign
Select item 3039604	NM_020859.4(SHROOM3):c.1413T>G (p.Pro471=)	SHROOM3, SHROOM3-AS1	Single nucleotide variant (synonymous variant)	SHROOM3-related disorder	GLikely benign
Select item 3038663	NM_020859.4(SHROOM3):c.556G>C (p.Gly186Arg)	SHROOM3, SHROOM3-AS1 (G186R)	Single nucleotide variant (missense variant)	SHROOM3-related disorder	GBenign
Select item 3038405	NM_020859.4(SHROOM3):c.2442C>T (p.Thr814=)	SHROOM3, SHROOM3-AS1	Single nucleotide variant (synonymous variant)	SHROOM3-related disorder	GLikely benign
Select item 3035613	NM_020859.4(SHROOM3):c.2643G>C (p.Pro881=)	SHROOM3, SHROOM3-AS1	Single nucleotide variant (synonymous variant)	SHROOM3-related disorder	GLikely benign
Select item 3034136	NM_020859.4(SHROOM3):c.4593T>A (p.Pro1531=)	SHROOM3, SHROOM3-AS1	Single nucleotide variant (synonymous variant)	SHROOM3-related disorder	GLikely benign
Select item 3024631	GRCh37/hg19 4p12-q35.2(chr4:45455621-191003541)x3	DDX60L, MTHFD2L +537 more	Copy number gain	not provided	GPathogenic
Select item 2681544	NM_020859.4(SHROOM3):c.3385G>A (p.Glu1129Lys)	SHROOM3, SHROOM3-AS1 (E1129K)	Single nucleotide variant (missense variant)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2654834	NM_020859.4(SHROOM3):c.4192C>T (p.Pro1398Ser)	SHROOM3, SHROOM3-AS1 (P1398S)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2654833	NM_020859.4(SHROOM3):c.3812C>G (p.Ala1271Gly)	SHROOM3, SHROOM3-AS1 (A1271G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2654832	NM_020859.4(SHROOM3):c.3492G>A (p.Gln1164=)	SHROOM3, SHROOM3-AS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2654831	NM_020859.4(SHROOM3):c.3474C>G (p.Ala1158=)	SHROOM3, SHROOM3-AS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2654830	NM_020859.4(SHROOM3):c.2849C>T (p.Ala950Val)	SHROOM3, SHROOM3-AS1 (A950V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2654829	NM_020859.4(SHROOM3):c.442C>T (p.Arg148Trp)	SHROOM3, SHROOM3-AS1 (R148W)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GUncertain significance
Select item 2636516	NM_020859.4(SHROOM3):c.3499C>T (p.Pro1167Ser)	SHROOM3, SHROOM3-AS1 (P1167S)	Single nucleotide variant (missense variant)	SHROOM3-related disorder	GUncertain significance
Select item 2620803	NM_020859.4(SHROOM3):c.1463A>G (p.Asn488Ser)	SHROOM3, SHROOM3-AS1 (N488S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617133	NM_020859.4(SHROOM3):c.2991G>T (p.Arg997Ser)	SHROOM3, SHROOM3-AS1 (R997S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613341	NM_020859.4(SHROOM3):c.3698C>T (p.Ala1233Val)	SHROOM3, SHROOM3-AS1 (A1233V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610835	NM_020859.4(SHROOM3):c.5603A>G (p.Asp1868Gly)	SHROOM3, SHROOM3-AS1 (D1868G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607323	NM_020859.4(SHROOM3):c.4417G>A (p.Asp1473Asn)	SHROOM3, SHROOM3-AS1 (D1473N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605134	NM_020859.4(SHROOM3):c.3571G>A (p.Gly1191Arg)	SHROOM3, SHROOM3-AS1 (G1191R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2604952	NM_020859.4(SHROOM3):c.4708A>G (p.Ser1570Gly)	SHROOM3, SHROOM3-AS1 (S1570G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600995	NM_020859.4(SHROOM3):c.1058G>A (p.Gly353Asp)	SHROOM3, SHROOM3-AS1 (G353D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599734	NM_020859.4(SHROOM3):c.1346A>G (p.Lys449Arg)	SHROOM3, SHROOM3-AS1 (K449R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595760	NM_020859.4(SHROOM3):c.822C>A (p.His274Gln)	SHROOM3, SHROOM3-AS1 (H274Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594412	NM_020859.4(SHROOM3):c.2906G>A (p.Arg969Gln)	SHROOM3, SHROOM3-AS1 (R969Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591182	NM_020859.4(SHROOM3):c.2143C>A (p.His715Asn)	SHROOM3, SHROOM3-AS1 (H715N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588857	NM_020859.4(SHROOM3):c.3508C>T (p.Arg1170Cys)	SHROOM3, SHROOM3-AS1 (R1170C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554957	NM_020859.4(SHROOM3):c.5713G>T (p.Val1905Leu)	SHROOM3, SHROOM3-AS1 (V1905L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551139	NM_020859.4(SHROOM3):c.2002A>G (p.Ile668Val)	SHROOM3, SHROOM3-AS1 (I668V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547194	NM_020859.4(SHROOM3):c.88G>A (p.Ala30Thr)	SHROOM3 (A30T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544652	NM_020859.4(SHROOM3):c.1230A>T (p.Lys410Asn)	SHROOM3, SHROOM3-AS1 (K410N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541331	NM_020859.4(SHROOM3):c.1177G>A (p.Ala393Thr)	SHROOM3, SHROOM3-AS1 (A393T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2538123	NM_020859.4(SHROOM3):c.2498G>A (p.Arg833His)	SHROOM3, SHROOM3-AS1 (R833H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2537202	NM_020859.4(SHROOM3):c.4199C>T (p.Pro1400Leu)	SHROOM3, SHROOM3-AS1 (P1400L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536178	NM_020859.4(SHROOM3):c.748A>T (p.Ser250Cys)	SHROOM3, SHROOM3-AS1 (S250C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534092	NM_020859.4(SHROOM3):c.890A>C (p.Glu297Ala)	SHROOM3, SHROOM3-AS1 (E297A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527424	NM_020859.4(SHROOM3):c.3913A>G (p.Lys1305Glu)	SHROOM3, SHROOM3-AS1 (K1305E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525913	NM_020859.4(SHROOM3):c.2948G>A (p.Arg983Gln)	SHROOM3, SHROOM3-AS1 (R983Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524705	NM_020859.4(SHROOM3):c.856A>G (p.Met286Val)	SHROOM3, SHROOM3-AS1 (M286V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524338	NM_020859.4(SHROOM3):c.5921C>T (p.Thr1974Met)	SHROOM3, SHROOM3-AS1 (T1974M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521855	NM_020859.4(SHROOM3):c.1054C>T (p.Arg352Trp)	SHROOM3, SHROOM3-AS1 (R352W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520921	NM_020859.4(SHROOM3):c.4775T>C (p.Val1592Ala)	SHROOM3, SHROOM3-AS1 (V1592A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516261	NM_020859.4(SHROOM3):c.4616C>T (p.Pro1539Leu)	SHROOM3, SHROOM3-AS1 (P1539L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2512731	NM_020859.4(SHROOM3):c.2942C>T (p.Thr981Met)	SHROOM3, SHROOM3-AS1 (T981M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476957	NM_020859.4(SHROOM3):c.5807G>A (p.Arg1936Gln)	SHROOM3, SHROOM3-AS1 (R1936Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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