ClinVar Miner

List of variants in gene AIFM2 reported by Ambry Genetics

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Total variants: 39
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HGVS dbSNP gnomAD frequency
NM_032797.6(AIFM2):c.920C>T (p.Ala307Val) rs149267164 0.00040
NM_032797.6(AIFM2):c.971G>A (p.Gly324Asp) rs142016168 0.00038
NM_032797.6(AIFM2):c.662G>A (p.Arg221Gln) rs143261580 0.00027
NM_032797.6(AIFM2):c.1043G>A (p.Arg348Gln) rs200384144 0.00014
NM_032797.6(AIFM2):c.565C>T (p.Arg189Trp) rs147089234 0.00013
NM_032797.6(AIFM2):c.44T>C (p.Val15Ala) rs922700901 0.00007
NM_032797.6(AIFM2):c.865G>A (p.Val289Met) rs148682063 0.00007
NM_032797.6(AIFM2):c.968C>T (p.Pro323Leu) rs376374471 0.00007
NM_032797.6(AIFM2):c.1088C>T (p.Thr363Met) rs146783519 0.00006
NM_032797.6(AIFM2):c.758G>A (p.Arg253His) rs145619443 0.00006
NM_032797.6(AIFM2):c.125T>C (p.Met42Thr) rs754619564 0.00005
NM_032797.6(AIFM2):c.26C>T (p.Ser9Leu) rs372676967 0.00005
NM_032797.6(AIFM2):c.562G>A (p.Val188Ile) rs137970860 0.00003
NM_032797.6(AIFM2):c.949C>G (p.Pro317Ala) rs368855181 0.00003
NM_032797.6(AIFM2):c.370A>G (p.Ser124Gly) rs1196426592 0.00002
NM_032797.6(AIFM2):c.913G>A (p.Ala305Thr) rs774471671 0.00002
NM_032797.6(AIFM2):c.1042C>T (p.Arg348Trp) rs542314841 0.00001
NM_032797.6(AIFM2):c.1069C>T (p.Arg357Trp) rs145638743 0.00001
NM_032797.6(AIFM2):c.146A>G (p.Asn49Ser) rs200533003 0.00001
NM_032797.6(AIFM2):c.227A>T (p.Asn76Ile) rs766635300 0.00001
NM_032797.6(AIFM2):c.326C>T (p.Thr109Met) rs374856767 0.00001
NM_032797.6(AIFM2):c.35T>C (p.Leu12Pro) rs1162566060 0.00001
NM_032797.6(AIFM2):c.49G>A (p.Val17Met) rs754745933 0.00001
NM_032797.6(AIFM2):c.566G>A (p.Arg189Gln) rs753854619 0.00001
NM_032797.6(AIFM2):c.1057C>A (p.Leu353Met)
NM_032797.6(AIFM2):c.1072G>A (p.Asp358Asn)
NM_032797.6(AIFM2):c.161G>A (p.Arg54Gln)
NM_032797.6(AIFM2):c.17C>T (p.Ser6Leu) rs775593494
NM_032797.6(AIFM2):c.184G>A (p.Ala62Thr) rs771696445
NM_032797.6(AIFM2):c.233G>A (p.Arg78Gln)
NM_032797.6(AIFM2):c.296C>T (p.Ala99Val)
NM_032797.6(AIFM2):c.550C>A (p.Leu184Ile)
NM_032797.6(AIFM2):c.601G>A (p.Val201Met)
NM_032797.6(AIFM2):c.653A>G (p.Asn218Ser)
NM_032797.6(AIFM2):c.812A>C (p.His271Pro)
NM_032797.6(AIFM2):c.872C>A (p.Thr291Lys)
NM_032797.6(AIFM2):c.895G>A (p.Gly299Ser)
NM_032797.6(AIFM2):c.947G>A (p.Arg316Gln)
NM_032797.6(AIFM2):c.973G>A (p.Ala325Thr)

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