"PreventionGenetics, part of Exact Sciences"[submitter] AND "XIRP2"[ge - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3039992	NM_152381.6(XIRP2):c.2T>C (p.Met1Thr)	XIRP2 (M1T)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GLikely benign
Select item 791155	NM_152381.6(XIRP2):c.10A>G (p.Met4Val)	XIRP2 (M4V)	Single nucleotide variant (missense variant)	XIRP2-related disorder +1 more	GBenign
Select item 2651512	NM_152381.6(XIRP2):c.21C>T (p.Gly7=)	XIRP2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 756167	NM_152381.6(XIRP2):c.216T>C (p.Ser72=)	XIRP2	Single nucleotide variant (synonymous variant)	XIRP2-related disorder +1 more	GLikely benign
Select item 3049522	NM_152381.6(XIRP2):c.461G>A (p.Gly154Glu)	XIRP2, XIRP2-AS1 (G154E)	Single nucleotide variant (missense variant)	XIRP2-related disorder	GLikely benign
Select item 3029807	NM_152381.6(XIRP2):c.563-26164C>T	XIRP2 (L198F)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GUncertain significance
Select item 789967	NM_152381.6(XIRP2):c.563-26158C>T	XIRP2 (L200F)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 711348	NM_152381.6(XIRP2):c.563-26147T>C	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder +1 more	GBenign/Likely benign
Select item 3056174	NM_152381.6(XIRP2):c.563-26093T>C	XIRP2	Single nucleotide variant (splice donor variant +1 more)	XIRP2-related disorder	GBenign
Select item 724596	NM_152381.6(XIRP2):c.753G>T (p.Val251=)	XIRP2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 724597	NM_152381.6(XIRP2):c.754C>T (p.Pro252Ser)	XIRP2 (P285S +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 729114	NM_152381.6(XIRP2):c.793G>A (p.Glu265Lys)	XIRP2 (E265K +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 722353	NM_152381.6(XIRP2):c.869A>G (p.His290Arg)	XIRP2 (H290R +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 780359	NM_152381.6(XIRP2):c.902A>T (p.Gln301Leu)	XIRP2 (Q301L +2 more)	Single nucleotide variant (missense variant)	XIRP2-related disorder +1 more	GBenign
Select item 3047590	NM_152381.6(XIRP2):c.997G>C (p.Glu333Gln)	XIRP2 (E111Q +2 more)	Single nucleotide variant (missense variant)	XIRP2-related disorder	GLikely benign
Select item 729115	NM_152381.6(XIRP2):c.1011A>C (p.Ala337=)	XIRP2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3055233	NM_152381.6(XIRP2):c.1026A>G (p.Gln342=)	XIRP2	Single nucleotide variant (synonymous variant)	XIRP2-related disorder	GLikely benign
Select item 3053544	NM_152381.6(XIRP2):c.1083G>A (p.Ser361=)	XIRP2	Single nucleotide variant (synonymous variant)	XIRP2-related disorder	GLikely benign
Select item 783987	NM_152381.6(XIRP2):c.1598G>A (p.Ser533Asn)	XIRP2 (S533N +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 3053584	NM_152381.6(XIRP2):c.1822A>G (p.Ile608Val)	XIRP2 (I386V +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 3058991	NM_152381.6(XIRP2):c.1836T>C (p.Gly612=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GBenign
Select item 3056252	NM_152381.6(XIRP2):c.1873C>G (p.Pro625Ala)	XIRP2 (P403A +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 3051006	NM_152381.6(XIRP2):c.1875C>G (p.Pro625=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GLikely benign
Select item 3059268	NM_152381.6(XIRP2):c.1894T>C (p.Tyr632His)	XIRP2 (Y410H +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 710895	NM_152381.6(XIRP2):c.2049C>T (p.Asp683=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder +1 more	GBenign/Likely benign
Select item 729116	NM_152381.6(XIRP2):c.2208C>T (p.Phe736=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 3058496	NM_152381.6(XIRP2):c.2223A>G (p.Leu741=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GLikely benign
Select item 721992	NM_152381.6(XIRP2):c.2311C>T (p.Arg771Trp)	XIRP2 (R549W +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 3059180	NM_152381.6(XIRP2):c.2541C>A (p.Thr847=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GBenign
Select item 729117	NM_152381.6(XIRP2):c.2557C>T (p.Leu853=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 731508	NM_152381.6(XIRP2):c.2587C>T (p.Gln863Ter)	XIRP2 (Q641* +1 more)	Single nucleotide variant (nonsense +1 more)	not provided +1 more	GBenign/Likely benign
Select item 3037902	NM_152381.6(XIRP2):c.3001G>A (p.Val1001Ile)	XIRP2 (V1001I +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 3056115	NM_152381.6(XIRP2):c.3003A>G (p.Val1001=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GBenign
Select item 3059357	NM_152381.6(XIRP2):c.3240T>G (p.Thr1080=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GBenign
Select item 3055561	NM_152381.6(XIRP2):c.3484G>A (p.Val1162Ile)	XIRP2 (V1162I +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 728645	NM_152381.6(XIRP2):c.3668T>C (p.Ile1223Thr)	XIRP2 (I1223T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 3033175	NM_152381.6(XIRP2):c.4077A>G (p.Leu1359=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GLikely benign
Select item 2651513	NM_152381.6(XIRP2):c.4128AGA[1] (p.Glu1377del)	XIRP2 (E1155del +1 more)	Microsatellite (inframe_deletion +1 more)	not provided +1 more	GLikely benign
Select item 3048657	NM_152381.6(XIRP2):c.4363C>T (p.Leu1455=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GBenign
Select item 3047829	NM_152381.6(XIRP2):c.4473G>A (p.Val1491=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GLikely benign
Select item 780360	NM_152381.6(XIRP2):c.4715T>C (p.Ile1572Thr)	XIRP2 (I1572T +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder +1 more	GBenign
Select item 3037603	NM_152381.6(XIRP2):c.4872G>T (p.Leu1624Phe)	XIRP2 (L1402F +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 716297	NM_152381.6(XIRP2):c.4915C>A (p.Gln1639Lys)	XIRP2 (Q1639K +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 780361	NM_152381.6(XIRP2):c.4988T>C (p.Ile1663Thr)	XIRP2 (I1663T +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder +1 more	GBenign
Select item 714940	NM_152381.6(XIRP2):c.5069C>T (p.Thr1690Ile)	XIRP2 (T1690I +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 724598	NM_152381.6(XIRP2):c.5114G>A (p.Arg1705His)	XIRP2 (R1705H +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 3033651	NM_152381.6(XIRP2):c.5291A>C (p.Glu1764Ala)	XIRP2 (E1542A +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GLikely benign
Select item 3038977	NM_152381.6(XIRP2):c.5331G>A (p.Glu1777=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GLikely benign
Select item 729118	NM_152381.6(XIRP2):c.5342T>C (p.Ile1781Thr)	XIRP2 (I1781T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 3056310	NM_152381.6(XIRP2):c.5402G>A (p.Arg1801His)	XIRP2 (R1579H +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 728646	NM_152381.6(XIRP2):c.5516G>A (p.Gly1839Asp)	XIRP2 (G1617D +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 3042830	NM_152381.6(XIRP2):c.5541C>G (p.Ser1847=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GLikely benign
Select item 3052804	NM_152381.6(XIRP2):c.5574G>A (p.Thr1858=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GBenign
Select item 3041096	NM_152381.6(XIRP2):c.5663C>A (p.Pro1888His)	XIRP2 (P1666H +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GLikely benign
Select item 3059886	NM_152381.6(XIRP2):c.5799A>G (p.Gln1933=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GBenign
Select item 3056250	NM_152381.6(XIRP2):c.5961G>A (p.Ala1987=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GBenign
Select item 3056298	NM_152381.6(XIRP2):c.6023A>G (p.Asn2008Ser)	XIRP2 (N1786S +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 711197	NM_152381.6(XIRP2):c.6048T>C (p.Val2016=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder +1 more	GBenign
Select item 786732	NM_152381.6(XIRP2):c.6281C>G (p.Thr2094Arg)	XIRP2 (T1872R +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder +1 more	GBenign
Select item 3056458	NM_152381.6(XIRP2):c.6297C>T (p.Asp2099=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GBenign
Select item 3057237	NM_152381.6(XIRP2):c.6468A>C (p.Thr2156=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GBenign
Select item 777567	NM_152381.6(XIRP2):c.6614A>C (p.Asn2205Thr)	XIRP2 (N2205T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 3055585	NM_152381.6(XIRP2):c.6725G>A (p.Arg2242Gln)	XIRP2 (R2020Q +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 3056187	NM_152381.6(XIRP2):c.7086G>T (p.Met2362Ile)	XIRP2 (M2140I +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 3039879	NM_152381.6(XIRP2):c.7095G>A (p.Pro2365=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GLikely benign
Select item 3045406	NM_152381.6(XIRP2):c.7290C>T (p.Pro2430=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GLikely benign
Select item 3044446	NM_152381.6(XIRP2):c.7548G>A (p.Ala2516=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GLikely benign
Select item 3035476	NM_152381.6(XIRP2):c.7719T>C (p.Thr2573=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GLikely benign
Select item 3041969	NM_152381.6(XIRP2):c.7793T>G (p.Leu2598Arg)	XIRP2 (L2376R +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 715398	NM_152381.6(XIRP2):c.7799G>A (p.Gly2600Glu)	XIRP2 (G2378E +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 781685	NM_152381.6(XIRP2):c.7856G>A (p.Arg2619Gln)	XIRP2 (R2619Q +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder +1 more	GBenign/Likely benign
Select item 3053758	NM_152381.6(XIRP2):c.7932T>C (p.His2644=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GLikely benign
Select item 3056737	NM_152381.6(XIRP2):c.8183G>A (p.Ser2728Asn)	XIRP2 (S2506N +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 788960	NM_152381.6(XIRP2):c.8308C>T (p.His2770Tyr)	XIRP2 (H2548Y +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder +1 more	GBenign
Select item 3032796	NM_152381.6(XIRP2):c.8343A>G (p.Thr2781=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GLikely benign
Select item 3059759	NM_152381.6(XIRP2):c.8344G>A (p.Val2782Ile)	XIRP2 (V2560I +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 3048215	NM_152381.6(XIRP2):c.8397G>A (p.Met2799Ile)	XIRP2 (M2577I +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 729119	NM_152381.6(XIRP2):c.8505A>G (p.Leu2835=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 728647	NM_152381.6(XIRP2):c.8577T>C (p.Asp2859=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 3049185	NM_152381.6(XIRP2):c.8689A>C (p.Lys2897Gln)	XIRP2 (K2675Q +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 3056874	NM_152381.6(XIRP2):c.8708G>A (p.Gly2903Asp)	XIRP2 (G2681D +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 719169	NM_152381.6(XIRP2):c.9126G>A (p.Pro3042=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 770131	NM_152381.6(XIRP2):c.9133A>G (p.Lys3045Glu)	XIRP2 (K3045E +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 3055785	NM_152381.6(XIRP2):c.9253G>A (p.Ala3085Thr)	XIRP2 (A2863T +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 724599	NM_152381.6(XIRP2):c.9449A>G (p.Tyr3150Cys)	XIRP2 (Y2928C +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign
Select item 783988	NM_152381.6(XIRP2):c.9450T>C (p.Tyr3150=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 3055980	NM_152381.6(XIRP2):c.9589A>G (p.Ile3197Val)	XIRP2 (I2975V +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 719317	NM_152381.6(XIRP2):c.9835T>C (p.Ser3279Pro)	XIRP2 (S3057P +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder +1 more	GBenign/Likely benign
Select item 724600	NM_152381.6(XIRP2):c.10110A>G (p.Thr3370=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign
Select item 3041604	NM_152381.6(XIRP2):c.10130G>A (p.Gly3377Glu)	XIRP2 (G3155E +1 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 3059797	NM_152381.6(XIRP2):c.10455A>G (p.Gln3485=)	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GBenign
Select item 3041864	NM_152381.6(XIRP2):c.10556-8A>G	XIRP2	Single nucleotide variant (intron variant)	XIRP2-related disorder	GBenign
Select item 3054262	NM_152381.6(XIRP2):c.*97A>G	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GLikely benign
Select item 779319	NM_152381.6(XIRP2):c.*240C>T	XIRP2 (T504I +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 3040214	NM_152381.6(XIRP2):c.*343T>C	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GBenign
Select item 3048284	NM_152381.6(XIRP2):c.*655G>A	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GLikely benign
Select item 3059285	NM_152381.6(XIRP2):c.*998A>G	XIRP2 (R535G +2 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign
Select item 3058410	NM_152381.6(XIRP2):c.*1042T>C	XIRP2	Single nucleotide variant (synonymous variant +1 more)	XIRP2-related disorder	GLikely benign
Select item 2651516	NM_152381.6(XIRP2):c.*1241T>C	XIRP2 (S616P +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign
Select item 3059726	NM_152381.6(XIRP2):c.*1383T>G	XIRP2 (V663G +2 more)	Single nucleotide variant (missense variant +1 more)	XIRP2-related disorder	GBenign

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