List of variants in gene ALDH5A1 reported as uncertain significance for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 42

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HGVS	dbSNP	gnomAD frequency
NM_001080.3(ALDH5A1):c.961G>A (p.Val321Met)	rs115784602	0.00349
NM_001080.3(ALDH5A1):c.1198G>A (p.Val400Ile)	rs147358733	0.00105
NM_001080.3(ALDH5A1):c.1421A>C (p.Asp474Ala)	rs142482046	0.00060
NM_001080.3(ALDH5A1):c.1107C>T (p.Arg369=)	rs148188703	0.00047
NM_001080.3(ALDH5A1):c.605C>T (p.Thr202Ile)	rs148733464	0.00043
NM_001080.3(ALDH5A1):c.1531G>A (p.Gly511Ser)	rs377658514	0.00041
NM_001080.3(ALDH5A1):c.1474G>A (p.Val492Ile)	rs151294087	0.00032
NM_001080.3(ALDH5A1):c.542C>T (p.Thr181Ile)	rs147439442	0.00026
NM_001080.3(ALDH5A1):c.518G>A (p.Arg173His)	rs369366567	0.00018
NM_001080.3(ALDH5A1):c.1308T>G (p.His436Gln)	rs199500997	0.00016
NM_001080.3(ALDH5A1):c.1316C>T (p.Thr439Ile)	rs139633130	0.00015
NM_001080.3(ALDH5A1):c.735C>G (p.Ser245Arg)	rs141430899	0.00015
NM_001080.3(ALDH5A1):c.1163C>T (p.Ala388Val)	rs536355368	0.00014
NM_001080.3(ALDH5A1):c.1280A>G (p.Asn427Ser)	rs149793005	0.00014
NM_001080.3(ALDH5A1):c.859A>G (p.Thr287Ala)	rs369156704	0.00013
NM_001080.3(ALDH5A1):c.862A>G (p.Thr288Ala)	rs373320785	0.00010
NM_001080.3(ALDH5A1):c.727-13T>G	rs187404409	0.00009
NM_001080.3(ALDH5A1):c.1211C>G (p.Ala404Gly)	rs139719918	0.00006
NM_001080.3(ALDH5A1):c.1169A>G (p.Glu390Gly)	rs142677472	0.00005
NM_001080.3(ALDH5A1):c.589G>A (p.Val197Met)	rs768219929	0.00004
NM_001080.3(ALDH5A1):c.1558G>A (p.Gly520Ser)	rs1179619995	0.00003
NM_001080.3(ALDH5A1):c.1606T>C (p.Ter536Gln)	rs201484501	0.00003
NM_001080.3(ALDH5A1):c.1343+8C>T	rs775916984	0.00002
NM_001080.3(ALDH5A1):c.1105C>T (p.Arg369Cys)	rs772038058	0.00001
NM_001080.3(ALDH5A1):c.1565A>G (p.Asp522Gly)	rs777938693	0.00001
NM_001080.3(ALDH5A1):c.514C>T (p.Arg172Cys)	rs551902853	0.00001
NM_001080.3(ALDH5A1):c.649G>A (p.Ala217Thr)	rs1064796319	0.00001
NM_001080.3(ALDH5A1):c.692A>G (p.Glu231Gly)	rs757605946	0.00001
NM_001080.3(ALDH5A1):c.786G>C (p.Lys262Asn)	rs766715554	0.00001
NM_001080.3(ALDH5A1):c.1052G>T (p.Gly351Val)
NM_001080.3(ALDH5A1):c.1325C>G (p.Pro442Arg)	rs2127389566
NM_001080.3(ALDH5A1):c.1348G>C (p.Asp450His)	rs144177566
NM_001080.3(ALDH5A1):c.1514G>A (p.Gly505Asp)	rs1449304427
NM_001080.3(ALDH5A1):c.1562T>C (p.Ile521Thr)	rs1475837931
NM_001080.3(ALDH5A1):c.496T>C (p.Trp166Arg)	rs2127382426
NM_001080.3(ALDH5A1):c.514C>G (p.Arg172Gly)	rs551902853
NM_001080.3(ALDH5A1):c.517C>A (p.Arg173Ser)	rs759155182
NM_001080.3(ALDH5A1):c.565C>G (p.Leu189Val)	rs1064796918
NM_001080.3(ALDH5A1):c.588C>T (p.Gly196=)	rs145208127
NM_001080.3(ALDH5A1):c.609G>T (p.Pro203=)	rs142373741
NM_001080.3(ALDH5A1):c.671C>T (p.Thr224Ile)
NM_001080.3(ALDH5A1):c.799G>T (p.Val267Leu)	rs1759546145

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