ClinVar Miner

List of variants in gene A2ML1 reported as likely benign for not specified

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Gene type:
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Total variants: 69
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HGVS dbSNP gnomAD frequency
NM_144670.6(A2ML1):c.3569C>T (p.Ala1190Val) rs73040625 0.05426
NM_144670.6(A2ML1):c.1937T>C (p.Ile646Thr) rs150488553 0.00158
NM_144670.6(A2ML1):c.2027G>A (p.Arg676Gln) rs138301233 0.00070
NM_144670.6(A2ML1):c.2197T>C (p.Phe733Leu) rs117213221 0.00051
NM_144670.6(A2ML1):c.1237G>A (p.Val413Ile) rs185181365 0.00047
NM_144670.6(A2ML1):c.911T>C (p.Ile304Thr) rs184575465 0.00042
NM_144670.6(A2ML1):c.3003G>A (p.Arg1001=) rs200269317 0.00041
NM_144670.6(A2ML1):c.1780G>A (p.Val594Met) rs201527641 0.00038
NM_144670.6(A2ML1):c.2395T>G (p.Ser799Ala) rs374408168 0.00026
NM_144670.6(A2ML1):c.4018C>A (p.Gln1340Lys) rs182743597 0.00023
NM_144670.6(A2ML1):c.2404C>T (p.Arg802Cys) rs367937691 0.00021
NM_144670.6(A2ML1):c.68A>G (p.Tyr23Cys) rs750524549 0.00019
NM_144670.6(A2ML1):c.1433C>T (p.Pro478Leu) rs201762847 0.00017
NM_144670.6(A2ML1):c.1856G>C (p.Trp619Ser) rs369180298 0.00014
NM_144670.6(A2ML1):c.277G>T (p.Val93Leu) rs775011475 0.00014
NM_144670.6(A2ML1):c.2405G>A (p.Arg802His) rs201562272 0.00013
NM_144670.6(A2ML1):c.2840C>T (p.Thr947Met) rs199873022 0.00013
NM_144670.6(A2ML1):c.1236C>T (p.Asp412=) rs375780803 0.00011
NM_144670.6(A2ML1):c.2773G>A (p.Ala925Thr) rs201363860 0.00011
NM_144670.6(A2ML1):c.2677C>T (p.Arg893Ter) rs199651558 0.00009
NM_144670.6(A2ML1):c.2328C>T (p.Phe776=) rs368663740 0.00008
NM_144670.6(A2ML1):c.1477-13T>C rs778863549 0.00007
NM_144670.6(A2ML1):c.1284G>A (p.Pro428=) rs753945399 0.00006
NM_144670.6(A2ML1):c.1746G>A (p.Gln582=) rs767420128 0.00006
NM_144670.6(A2ML1):c.2441A>G (p.Asn814Ser) rs760788803 0.00006
NM_144670.6(A2ML1):c.4061+11_4061+12del rs767089812 0.00006
NM_144670.6(A2ML1):c.418C>T (p.Arg140Cys) rs199919065 0.00006
NM_144670.6(A2ML1):c.973G>A (p.Val325Met) rs749156731 0.00006
NM_144670.6(A2ML1):c.201A>G (p.Glu67=) rs371564965 0.00005
NM_144670.6(A2ML1):c.2984C>T (p.Thr995Met) rs755702632 0.00005
NM_144670.6(A2ML1):c.1440T>C (p.Asp480=) rs764291805 0.00004
NM_144670.6(A2ML1):c.2114T>C (p.Met705Thr) rs748085779 0.00004
NM_144670.6(A2ML1):c.2259C>T (p.His753=) rs747555996 0.00004
NM_144670.6(A2ML1):c.2260G>A (p.Val754Ile) rs769726608 0.00004
NM_144670.6(A2ML1):c.2486C>T (p.Ser829Leu) rs758305694 0.00004
NM_144670.6(A2ML1):c.3154A>G (p.Ile1052Val) rs753161669 0.00004
NM_144670.6(A2ML1):c.3935C>T (p.Thr1312Met) rs201083574 0.00004
NM_144670.6(A2ML1):c.2658G>A (p.Gly886=) rs762588799 0.00003
NM_144670.6(A2ML1):c.3384C>G (p.Ala1128=) rs773681065 0.00003
NM_144670.6(A2ML1):c.2310T>C (p.Thr770=) rs370481255 0.00002
NM_144670.6(A2ML1):c.3503-3T>C rs748270792 0.00002
NM_144670.6(A2ML1):c.3685C>T (p.His1229Tyr) rs764222230 0.00002
NM_144670.6(A2ML1):c.1704C>G (p.Pro568=) rs780752277 0.00001
NM_144670.6(A2ML1):c.2119+9C>T rs1428382436 0.00001
NM_144670.6(A2ML1):c.3495C>G (p.Ile1165Met) rs868320081 0.00001
NM_144670.6(A2ML1):c.4000G>C (p.Gly1334Arg) rs1052149878 0.00001
NM_144670.6(A2ML1):c.906C>T (p.Asp302=) rs1943356243 0.00001
NM_144670.5(A2ML1):c.-50C>G rs781435396
NM_144670.6(A2ML1):c.-16T>C rs369625679
NM_144670.6(A2ML1):c.137G>A (p.Gly46Glu) rs757200771
NM_144670.6(A2ML1):c.1569C>A (p.Thr523=) rs1455152222
NM_144670.6(A2ML1):c.159G>A (p.Thr53=) rs767370461
NM_144670.6(A2ML1):c.1662C>T (p.Val554=)
NM_144670.6(A2ML1):c.1769C>T (p.Ala590Val) rs770246364
NM_144670.6(A2ML1):c.1775G>A (p.Arg592Gln) rs200673370
NM_144670.6(A2ML1):c.1992G>A (p.Ser664=) rs765976469
NM_144670.6(A2ML1):c.2712+16del rs1555113735
NM_144670.6(A2ML1):c.2764+20del rs764632191
NM_144670.6(A2ML1):c.3124A>G (p.Thr1042Ala) rs565930773
NM_144670.6(A2ML1):c.3294T>G (p.Thr1098=) rs764429289
NM_144670.6(A2ML1):c.3346A>G (p.Met1116Val) rs79889829
NM_144670.6(A2ML1):c.3393G>A (p.Thr1131=)
NM_144670.6(A2ML1):c.3431del (p.Phe1144fs) rs776004500
NM_144670.6(A2ML1):c.3447A>G (p.Glu1149=)
NM_144670.6(A2ML1):c.3462C>T (p.Asn1154=)
NM_144670.6(A2ML1):c.540T>C (p.Ile180=) rs377551636
NM_144670.6(A2ML1):c.619G>T (p.Gly207Cys) rs11047499
NM_144670.6(A2ML1):c.888G>A (p.Val296=)
NM_144670.6(A2ML1):c.921G>C (p.Ala307=) rs372520121

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