ClinVar Miner

List of variants in gene ALDH7A1 studied for not specified

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Gene type:
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Total variants: 74
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HGVS dbSNP
NM_001182.4(ALDH7A1):c.-29T>C rs556650006
NM_001182.4(ALDH7A1):c.-30C>T rs760633380
NM_001182.4(ALDH7A1):c.-34G>C rs140627539
NM_001182.4(ALDH7A1):c.651-25_651-20delCTTTTT rs781687339
NM_001182.5(ALDH7A1):c.*5G>A rs759591318
NM_001182.5(ALDH7A1):c.-13T>G rs774190967
NM_001182.5(ALDH7A1):c.-18C>G rs796052254
NM_001182.5(ALDH7A1):c.1009-14C>T rs1057520220
NM_001182.5(ALDH7A1):c.1009-6G>A rs138056453
NM_001182.5(ALDH7A1):c.1017T>C (p.His339=) rs200394848
NM_001182.5(ALDH7A1):c.1022G>A (p.Ser341Asn) rs141701364
NM_001182.5(ALDH7A1):c.1069A>G (p.Ile357Val) rs761011399
NM_001182.5(ALDH7A1):c.1094-14T>G rs1057521816
NM_001182.5(ALDH7A1):c.1094-20C>G rs113775968
NM_001182.5(ALDH7A1):c.1094-4C>T rs977039138
NM_001182.5(ALDH7A1):c.1201-5A>G rs753508557
NM_001182.5(ALDH7A1):c.120G>A (p.Ala40=) rs1554101953
NM_001182.5(ALDH7A1):c.1233G>A (p.Pro411=) rs572831296
NM_001182.5(ALDH7A1):c.1234A>G (p.Thr412Ala) rs2306618
NM_001182.5(ALDH7A1):c.1263G>A (p.Ala421=) rs587780850
NM_001182.5(ALDH7A1):c.1287T>C (p.Phe429=) rs375030056
NM_001182.5(ALDH7A1):c.1305C>G (p.Val435=) rs142975776
NM_001182.5(ALDH7A1):c.1315A>C (p.Lys439Gln) rs12514417
NM_001182.5(ALDH7A1):c.1317+19C>T rs368215460
NM_001182.5(ALDH7A1):c.1317+20G>A rs17597559
NM_001182.5(ALDH7A1):c.1317+20G>C rs17597559
NM_001182.5(ALDH7A1):c.1318-16A>G rs879606419
NM_001182.5(ALDH7A1):c.133C>T (p.Leu45=) rs757162735
NM_001182.5(ALDH7A1):c.1376T>C (p.Ile459Thr) rs1057518529
NM_001182.5(ALDH7A1):c.1415+7C>T rs1057520741
NM_001182.5(ALDH7A1):c.1416-11T>C rs577675361
NM_001182.5(ALDH7A1):c.1470T>C (p.Ala490=) rs1057520651
NM_001182.5(ALDH7A1):c.1489+4C>T rs775065938
NM_001182.5(ALDH7A1):c.1490-7T>C rs1057522259
NM_001182.5(ALDH7A1):c.1565+15T>C rs375505703
NM_001182.5(ALDH7A1):c.1567A>G (p.Thr523Ala) rs61757684
NM_001182.5(ALDH7A1):c.192+9G>A rs1554101934
NM_001182.5(ALDH7A1):c.193-20C>T rs199762757
NM_001182.5(ALDH7A1):c.201G>T (p.Thr67=) rs747643987
NM_001182.5(ALDH7A1):c.222C>T (p.Asn74=) rs1007871645
NM_001182.5(ALDH7A1):c.23T>C (p.Leu8Pro) rs796052255
NM_001182.5(ALDH7A1):c.243A>G (p.Arg81=) rs146438406
NM_001182.5(ALDH7A1):c.246+6A>T rs759910341
NM_001182.5(ALDH7A1):c.273T>C (p.Thr91=) rs60720055
NM_001182.5(ALDH7A1):c.313-15G>A rs201720741
NM_001182.5(ALDH7A1):c.31_33delinsGAG (p.His11Glu) rs796052269
NM_001182.5(ALDH7A1):c.328C>G (p.Arg110Gly) rs121912708
NM_001182.5(ALDH7A1):c.354C>T (p.Gly118=) rs149228266
NM_001182.5(ALDH7A1):c.364C>T (p.Arg122Trp) rs370624118
NM_001182.5(ALDH7A1):c.373A>G (p.Ile125Val) rs117295656
NM_001182.5(ALDH7A1):c.393+12T>C rs1057522818
NM_001182.5(ALDH7A1):c.393+15T>C rs183254966
NM_001182.5(ALDH7A1):c.39A>G (p.Ala13=) rs201566142
NM_001182.5(ALDH7A1):c.450T>C (p.Tyr150=) rs375095250
NM_001182.5(ALDH7A1):c.518-12T>G rs79544459
NM_001182.5(ALDH7A1):c.552C>T (p.Pro184=) rs369859575
NM_001182.5(ALDH7A1):c.561G>A (p.Leu187=) rs1057523720
NM_001182.5(ALDH7A1):c.573C>T (p.Ile191=) rs1554100447
NM_001182.5(ALDH7A1):c.615C>T (p.Asn205=) rs369380330
NM_001182.5(ALDH7A1):c.63T>C (p.Pro21=) rs368427726
NM_001182.5(ALDH7A1):c.650+15C>G rs773601863
NM_001182.5(ALDH7A1):c.650+18T>C rs570318899
NM_001182.5(ALDH7A1):c.651-19T>A rs1057521334
NM_001182.5(ALDH7A1):c.675C>T (p.Leu225=) rs57902950
NM_001182.5(ALDH7A1):c.696-3T>C rs749516893
NM_001182.5(ALDH7A1):c.771T>C (p.Ile257=) rs1057520469
NM_001182.5(ALDH7A1):c.774-18G>A rs185333013
NM_001182.5(ALDH7A1):c.774-19C>T rs373058643
NM_001182.5(ALDH7A1):c.858G>A (p.Val286=) rs150623275
NM_001182.5(ALDH7A1):c.871+14T>A rs1554099737
NM_001182.5(ALDH7A1):c.913+8T>C rs766528289
NM_001182.5(ALDH7A1):c.914-13G>C rs148928130
NM_001182.5(ALDH7A1):c.960C>T (p.Phe320=) rs114516357
NM_001182.5(ALDH7A1):c.998C>T (p.Ala333Val) rs144625212

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