ClinVar for Gene (Select 10721) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 100 of 3290

<< First< Prev

Page of 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3351023	NM_199420.4(POLQ):c.1960-8C>T	POLQ	Single nucleotide variant (intron variant)	POLQ-related disorder	GLikely benign
Select item 3308760	NM_199420.4(POLQ):c.7017G>T (p.Leu2339Phe)	POLQ (L2339F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308758	NM_199420.4(POLQ):c.6022A>G (p.Ile2008Val)	POLQ (I2008V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308757	NM_199420.4(POLQ):c.3000G>C (p.Lys1000Asn)	POLQ (K1000N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308756	NM_199420.4(POLQ):c.1847C>T (p.Ser616Leu)	POLQ (S616L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308754	NM_199420.4(POLQ):c.6353A>G (p.Tyr2118Cys)	POLQ (Y2118C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308753	NM_199420.4(POLQ):c.3685A>G (p.Arg1229Gly)	POLQ (R1229G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308752	NM_199420.4(POLQ):c.1076G>A (p.Arg359Gln)	POLQ (R359Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308751	NM_199420.4(POLQ):c.2811G>T (p.Lys937Asn)	POLQ (K937N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308750	NM_199420.4(POLQ):c.294G>A (p.Glu98=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308749	NM_199420.4(POLQ):c.129C>A (p.Pro43=)	LOC112872292, POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308748	NM_199420.4(POLQ):c.6859A>C (p.Lys2287Gln)	POLQ (K2287Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308747	NM_199420.4(POLQ):c.7308A>G (p.Arg2436=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308745	NM_199420.4(POLQ):c.6664C>A (p.Pro2222Thr)	POLQ (P2222T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308744	NM_199420.4(POLQ):c.427A>G (p.Ile143Val)	POLQ (I143V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308743	NM_199420.4(POLQ):c.4521G>T (p.Met1507Ile)	POLQ (M1507I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308742	NM_199420.4(POLQ):c.5963A>C (p.Asp1988Ala)	POLQ (D1988A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308741	NM_199420.4(POLQ):c.6099G>A (p.Gly2033=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308740	NM_199420.4(POLQ):c.1342T>C (p.Ser448Pro)	POLQ (S448P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308739	NM_199420.4(POLQ):c.6347A>C (p.Gln2116Pro)	POLQ (Q2116P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308738	NM_199420.4(POLQ):c.2963C>G (p.Ala988Gly)	POLQ (A988G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308737	NM_199420.4(POLQ):c.1839T>A (p.His613Gln)	POLQ (H613Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308736	NM_199420.4(POLQ):c.6192G>A (p.Leu2064=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308734	NM_199420.4(POLQ):c.45A>G (p.Ser15=)	LOC112872292, POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308733	NM_199420.4(POLQ):c.7234T>C (p.Tyr2412His)	POLQ (Y2412H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308732	NM_199420.4(POLQ):c.433C>T (p.Pro145Ser)	POLQ (P145S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308731	NM_199420.4(POLQ):c.384T>G (p.Leu128=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308730	NM_199420.4(POLQ):c.4642T>A (p.Leu1548Met)	POLQ (L1548M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308729	NM_199420.4(POLQ):c.2958C>G (p.Phe986Leu)	POLQ (F986L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308728	NM_199420.4(POLQ):c.4337T>C (p.Leu1446Pro)	POLQ (L1446P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308727	NM_199420.4(POLQ):c.2008T>G (p.Phe670Val)	POLQ (F670V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308726	NM_199420.4(POLQ):c.1957C>G (p.Leu653Val)	POLQ (L653V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308725	NM_199420.4(POLQ):c.7767T>C (p.Asp2589=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308723	NM_199420.4(POLQ):c.792G>A (p.Met264Ile)	POLQ (M264I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308722	NM_199420.4(POLQ):c.6787C>T (p.Leu2263=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308721	NM_199420.4(POLQ):c.3597A>G (p.Gln1199=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308720	NM_199420.4(POLQ):c.5977T>C (p.Cys1993Arg)	POLQ (C1993R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308719	NM_199420.4(POLQ):c.5516C>T (p.Thr1839Ile)	POLQ (T1839I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308718	NM_199420.4(POLQ):c.4826G>T (p.Gly1609Val)	POLQ (G1609V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308717	NM_199420.4(POLQ):c.2858C>A (p.Pro953Gln)	POLQ (P953Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308716	NM_199420.4(POLQ):c.4766G>A (p.Arg1589Lys)	POLQ (R1589K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308715	NM_199420.4(POLQ):c.2185A>G (p.Ile729Val)	POLQ (I729V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308714	NM_199420.4(POLQ):c.6861G>A (p.Lys2287=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308712	NM_199420.4(POLQ):c.7687G>C (p.Glu2563Gln)	POLQ (E2563Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308711	NM_199420.4(POLQ):c.3896C>G (p.Thr1299Arg)	POLQ (T1299R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308710	NM_199420.4(POLQ):c.7235A>C (p.Tyr2412Ser)	POLQ (Y2412S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308709	NM_199420.4(POLQ):c.5287A>T (p.Asn1763Tyr)	POLQ (N1763Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308708	NM_199420.4(POLQ):c.1741G>T (p.Ala581Ser)	POLQ (A581S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308707	NM_199420.4(POLQ):c.3407A>G (p.His1136Arg)	POLQ (H1136R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308706	NM_199420.4(POLQ):c.7261A>G (p.Thr2421Ala)	POLQ (T2421A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308705	NM_199420.4(POLQ):c.6610A>C (p.Thr2204Pro)	POLQ (T2204P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308704	NM_199420.4(POLQ):c.1231T>C (p.Trp411Arg)	POLQ (W411R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308703	NM_199420.4(POLQ):c.3678C>T (p.Tyr1226=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308700	NM_199420.4(POLQ):c.2745G>T (p.Glu915Asp)	POLQ (E915D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308699	NM_199420.4(POLQ):c.4877A>G (p.Asn1626Ser)	POLQ (N1626S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308698	NM_199420.4(POLQ):c.3739A>G (p.Asn1247Asp)	POLQ (N1247D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308697	NM_199420.4(POLQ):c.2768T>C (p.Phe923Ser)	POLQ (F923S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308696	NM_199420.4(POLQ):c.3191G>T (p.Arg1064Ile)	POLQ (R1064I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308695	NM_199420.4(POLQ):c.3091A>T (p.Asn1031Tyr)	POLQ (N1031Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308694	NM_199420.4(POLQ):c.3399T>C (p.Phe1133=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308693	NM_199420.4(POLQ):c.77A>C (p.Asp26Ala)	LOC112872292, POLQ (D26A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308692	NM_199420.4(POLQ):c.1884T>A (p.Thr628=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308691	NM_199420.4(POLQ):c.6965C>G (p.Pro2322Arg)	POLQ (P2322R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308689	NM_199420.4(POLQ):c.5851T>G (p.Cys1951Gly)	POLQ (C1951G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308688	NM_199420.4(POLQ):c.1249C>T (p.His417Tyr)	POLQ (H417Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308687	NM_199420.4(POLQ):c.7272T>G (p.Asn2424Lys)	POLQ (N2424K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308686	NM_199420.4(POLQ):c.6185C>G (p.Ser2062Cys)	POLQ (S2062C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308685	NM_199420.4(POLQ):c.1092A>G (p.Leu364=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308684	NM_199420.4(POLQ):c.1001T>C (p.Ile334Thr)	POLQ (I334T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308683	NM_199420.4(POLQ):c.6316A>G (p.Met2106Val)	POLQ (M2106V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308682	NM_199420.4(POLQ):c.3337T>C (p.Ser1113Pro)	POLQ (S1113P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308681	NM_199420.4(POLQ):c.458A>G (p.Lys153Arg)	POLQ (K153R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308679	NM_199420.4(POLQ):c.7361A>G (p.Lys2454Arg)	POLQ (K2454R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308678	NM_199420.4(POLQ):c.6137C>T (p.Ala2046Val)	POLQ (A2046V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308677	NM_199420.4(POLQ):c.2449A>C (p.Thr817Pro)	POLQ (T817P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308676	NM_199420.4(POLQ):c.4835A>G (p.Asp1612Gly)	POLQ (D1612G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308675	NM_199420.4(POLQ):c.5660A>G (p.Asp1887Gly)	POLQ (D1887G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308674	NM_199420.4(POLQ):c.3783A>C (p.Arg1261Ser)	POLQ (R1261S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3308673	NM_199420.4(POLQ):c.3537C>T (p.Asn1179=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308672	NM_199420.4(POLQ):c.3955G>C (p.Glu1319Gln)	POLQ (E1319Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308671	NM_199420.4(POLQ):c.4758A>T (p.Val1586=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308670	NM_199420.4(POLQ):c.1257T>G (p.Gly419=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308668	NM_199420.4(POLQ):c.6410T>C (p.Leu2137Ser)	POLQ (L2137S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308667	NM_199420.4(POLQ):c.5868T>C (p.Ser1956=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308666	NM_199420.4(POLQ):c.3325G>C (p.Asp1109His)	POLQ (D1109H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308665	NM_199420.4(POLQ):c.945C>G (p.Pro315=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308664	NM_199420.4(POLQ):c.6765T>C (p.Asp2255=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308663	NM_199420.4(POLQ):c.3404A>C (p.Glu1135Ala)	POLQ (E1135A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308662	NM_199420.4(POLQ):c.5722G>A (p.Gly1908Ser)	POLQ (G1908S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308661	NM_199420.4(POLQ):c.1904T>C (p.Leu635Pro)	POLQ (L635P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308660	NM_199420.4(POLQ):c.1546C>G (p.Arg516Gly)	POLQ (R516G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308659	NM_199420.4(POLQ):c.1890T>C (p.Asp630=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308657	NM_199420.4(POLQ):c.1137A>G (p.Pro379=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308656	NM_199420.4(POLQ):c.3935G>A (p.Gly1312Asp)	POLQ (G1312D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308655	NM_199420.4(POLQ):c.4037A>C (p.Asp1346Ala)	POLQ (D1346A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308654	NM_199420.4(POLQ):c.3236A>G (p.Glu1079Gly)	POLQ (E1079G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308653	NM_199420.4(POLQ):c.4375A>G (p.Ile1459Val)	POLQ (I1459V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308652	NM_199420.4(POLQ):c.264T>C (p.Gly88=)	POLQ	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3308651	NM_199420.4(POLQ):c.116T>C (p.Leu39Pro)	LOC112872292, POLQ (L39P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3308650	NM_199420.4(POLQ):c.1114G>C (p.Val372Leu)	POLQ (V372L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

<< First< Prev

Page of 33