ClinVar Miner

List of variants in gene ADAT1 reported as uncertain significance

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Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_001324445.2(ADAT1):c.1250A>G (p.Gln417Arg) rs147999655 0.00027
NM_001324445.2(ADAT1):c.157A>G (p.Lys53Glu) rs150142918 0.00013
NM_001324445.2(ADAT1):c.683C>T (p.Pro228Leu) rs560668562 0.00012
NM_001324445.2(ADAT1):c.914G>A (p.Arg305Gln) rs199507210 0.00012
NM_001324445.2(ADAT1):c.310C>T (p.Leu104Phe) rs1436996438 0.00008
NM_001324445.2(ADAT1):c.1232C>T (p.Thr411Ile) rs762604498 0.00007
NM_001324445.2(ADAT1):c.367G>A (p.Gly123Arg) rs144186738 0.00007
NM_001324445.2(ADAT1):c.826G>T (p.Ala276Ser) rs756353591 0.00006
NM_001324445.2(ADAT1):c.13G>A (p.Asp5Asn) rs369100478 0.00005
NM_001324445.2(ADAT1):c.621G>C (p.Glu207Asp) rs374204618 0.00005
NM_001324445.2(ADAT1):c.632G>A (p.Gly211Glu) rs748053472 0.00004
NM_001324445.2(ADAT1):c.149C>A (p.Thr50Asn) rs775552444 0.00003
NM_001324445.2(ADAT1):c.577G>A (p.Val193Ile) rs754541349 0.00003
NM_001324445.2(ADAT1):c.722C>G (p.Ala241Gly) rs138724951 0.00003
NM_001324445.2(ADAT1):c.821C>T (p.Pro274Leu) rs755063906 0.00003
NM_001324445.2(ADAT1):c.1048C>G (p.Gln350Glu) rs1478491353 0.00002
NM_001324445.2(ADAT1):c.1136C>T (p.Ala379Val) rs762132802 0.00001
NM_001324445.2(ADAT1):c.1192A>G (p.Ile398Val) rs150544374 0.00001
NM_001324445.2(ADAT1):c.1262A>G (p.Lys421Arg) rs2081422909 0.00001
NM_001324445.2(ADAT1):c.1351A>G (p.Arg451Gly) rs761013553 0.00001
NM_001324445.2(ADAT1):c.1418C>T (p.Ala473Val) rs754878846 0.00001
NM_001324445.2(ADAT1):c.525T>A (p.Ser175Arg) rs536106427 0.00001
NM_001324445.2(ADAT1):c.610G>A (p.Ala204Thr) rs368488673 0.00001
NM_001324445.2(ADAT1):c.817A>G (p.Lys273Glu) rs562128733 0.00001
NM_001324445.2(ADAT1):c.875A>G (p.Asp292Gly) rs1222009330 0.00001
NM_001324445.2(ADAT1):c.925C>T (p.Leu309Phe) rs745981176 0.00001
NM_001324445.2(ADAT1):c.928G>A (p.Gly310Arg) rs1462755168 0.00001
NM_001324445.2(ADAT1):c.99A>T (p.Leu33Phe) rs770664031 0.00001
NM_001324445.2(ADAT1):c.1026G>T (p.Gln342His) rs768314305
NM_001324445.2(ADAT1):c.1065A>T (p.Leu355Phe) rs1490648457
NM_001324445.2(ADAT1):c.1066C>G (p.Pro356Ala)
NM_001324445.2(ADAT1):c.1096A>G (p.Ile366Val)
NM_001324445.2(ADAT1):c.1136C>A (p.Ala379Glu) rs762132802
NM_001324445.2(ADAT1):c.1138G>A (p.Val380Met)
NM_001324445.2(ADAT1):c.1138G>C (p.Val380Leu) rs751762218
NM_001324445.2(ADAT1):c.1138G>T (p.Val380Leu)
NM_001324445.2(ADAT1):c.1234G>A (p.Ala412Thr)
NM_001324445.2(ADAT1):c.1370C>T (p.Ser457Phe) rs749428527
NM_001324445.2(ADAT1):c.1451G>A (p.Arg484Gln)
NM_001324445.2(ADAT1):c.145G>A (p.Asp49Asn)
NM_001324445.2(ADAT1):c.1465G>C (p.Gly489Arg) rs776176191
NM_001324445.2(ADAT1):c.175A>G (p.Lys59Glu)
NM_001324445.2(ADAT1):c.229A>G (p.Arg77Gly)
NM_001324445.2(ADAT1):c.259C>T (p.His87Tyr)
NM_001324445.2(ADAT1):c.274G>C (p.Ala92Pro)
NM_001324445.2(ADAT1):c.35A>G (p.Tyr12Cys)
NM_001324445.2(ADAT1):c.391C>T (p.Leu131Phe)
NM_001324445.2(ADAT1):c.431A>G (p.Asp144Gly)
NM_001324445.2(ADAT1):c.591G>A (p.Met197Ile)
NM_001324445.2(ADAT1):c.674C>G (p.Pro225Arg) rs193920811
NM_001324445.2(ADAT1):c.743C>A (p.Pro248His)
NM_001324445.2(ADAT1):c.766G>C (p.Val256Leu)
NM_001324445.2(ADAT1):c.806G>A (p.Gly269Glu)
NM_001324445.2(ADAT1):c.827C>T (p.Ala276Val)
NM_001324445.2(ADAT1):c.887C>T (p.Ser296Phe)
NM_001324445.2(ADAT1):c.966G>T (p.Glu322Asp)

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