ClinVar Miner

List of variants in gene SLC37A1 studied for not specified

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Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_001320537.2(SLC37A1):c.334G>A (p.Val112Met) rs140640546 0.00056
NM_001320537.2(SLC37A1):c.1588T>C (p.Phe530Leu) rs147676461 0.00048
NM_001320537.2(SLC37A1):c.1219A>G (p.Thr407Ala) rs143967583 0.00044
NM_001320537.2(SLC37A1):c.941G>A (p.Gly314Asp) rs143310994 0.00042
NM_001320537.2(SLC37A1):c.25C>T (p.Arg9Cys) rs546388927 0.00025
NM_001320537.2(SLC37A1):c.1108A>T (p.Thr370Ser) rs757553257 0.00013
NM_001320537.2(SLC37A1):c.1267A>G (p.Ile423Val) rs372412272 0.00011
NM_001320537.2(SLC37A1):c.403C>T (p.Leu135Phe) rs770907226 0.00011
NM_001320537.2(SLC37A1):c.742G>A (p.Val248Ile) rs370200672 0.00011
NM_001320537.2(SLC37A1):c.8G>A (p.Arg3Gln) rs201465099 0.00011
NM_001320537.2(SLC37A1):c.1210G>A (p.Ala404Thr) rs148432187 0.00009
NM_001320537.2(SLC37A1):c.604G>A (p.Val202Met) rs200166607 0.00008
NM_001320537.2(SLC37A1):c.1066A>C (p.Asn356His) rs771382208 0.00007
NM_001320537.2(SLC37A1):c.949G>A (p.Ala317Thr) rs201802080 0.00007
NM_001320537.2(SLC37A1):c.368G>A (p.Arg123His) rs762431393 0.00006
NM_001320537.2(SLC37A1):c.1330G>A (p.Val444Ile) rs779432325 0.00005
NM_001320537.2(SLC37A1):c.466G>A (p.Gly156Arg) rs144523117 0.00005
NM_001320537.2(SLC37A1):c.1211C>T (p.Ala404Val) rs576076453 0.00003
NM_001320537.2(SLC37A1):c.343T>A (p.Tyr115Asn) rs1263323684 0.00003
NM_001320537.2(SLC37A1):c.839A>G (p.Asn280Ser) rs559765596 0.00003
NM_001320537.2(SLC37A1):c.1187C>T (p.Thr396Ile) rs991887652 0.00002
NM_001320537.2(SLC37A1):c.16G>A (p.Ala6Thr) rs1264470149 0.00002
NM_001320537.2(SLC37A1):c.1101G>C (p.Glu367Asp) rs763231942 0.00001
NM_001320537.2(SLC37A1):c.1339G>A (p.Asp447Asn) rs759182256 0.00001
NM_001320537.2(SLC37A1):c.217G>A (p.Ala73Thr) rs767500155 0.00001
NM_001320537.2(SLC37A1):c.250G>A (p.Asp84Asn) rs1237483170 0.00001
NM_001320537.2(SLC37A1):c.64G>A (p.Ala22Thr) rs1292976429 0.00001
NM_001320537.2(SLC37A1):c.808C>A (p.Leu270Ile) rs2055624144 0.00001
NM_001320537.2(SLC37A1):c.1064C>T (p.Thr355Met)
NM_001320537.2(SLC37A1):c.1076A>G (p.His359Arg) rs1275628196
NM_001320537.2(SLC37A1):c.1100A>T (p.Glu367Val)
NM_001320537.2(SLC37A1):c.1102C>A (p.Leu368Ile) rs764281791
NM_001320537.2(SLC37A1):c.1139G>C (p.Gly380Ala) rs1472581025
NM_001320537.2(SLC37A1):c.1166G>A (p.Arg389Gln)
NM_001320537.2(SLC37A1):c.1180G>T (p.Ala394Ser)
NM_001320537.2(SLC37A1):c.1192G>A (p.Gly398Ser)
NM_001320537.2(SLC37A1):c.1228A>C (p.Ile410Leu) rs1276066163
NM_001320537.2(SLC37A1):c.1253G>A (p.Gly418Glu)
NM_001320537.2(SLC37A1):c.1333T>G (p.Ser445Ala)
NM_001320537.2(SLC37A1):c.152A>G (p.Lys51Arg)
NM_001320537.2(SLC37A1):c.1552A>G (p.Ser518Gly)
NM_001320537.2(SLC37A1):c.1574G>A (p.Gly525Glu)
NM_001320537.2(SLC37A1):c.172G>A (p.Glu58Lys) rs776285730
NM_001320537.2(SLC37A1):c.208T>A (p.Ser70Thr)
NM_001320537.2(SLC37A1):c.224C>T (p.Pro75Leu)
NM_001320537.2(SLC37A1):c.226C>G (p.His76Asp) rs780378552
NM_001320537.2(SLC37A1):c.235C>T (p.Pro79Ser)
NM_001320537.2(SLC37A1):c.346C>A (p.Leu116Ile)
NM_001320537.2(SLC37A1):c.367C>T (p.Arg123Cys) rs1242098177
NM_001320537.2(SLC37A1):c.449A>G (p.Tyr150Cys) rs150186814
NM_001320537.2(SLC37A1):c.541G>A (p.Gly181Ser)
NM_001320537.2(SLC37A1):c.65C>G (p.Ala22Gly)
NM_001320537.2(SLC37A1):c.670G>A (p.Val224Ile)
NM_001320537.2(SLC37A1):c.725T>C (p.Ile242Thr)
NM_001320537.2(SLC37A1):c.732T>G (p.His244Gln)
NM_001320537.2(SLC37A1):c.807A>C (p.Arg269Ser)
NM_001320537.2(SLC37A1):c.829A>G (p.Ser277Gly)
NM_001320537.2(SLC37A1):c.889G>A (p.Gly297Ser)
NM_001320537.2(SLC37A1):c.902C>T (p.Pro301Leu)
NM_001320537.2(SLC37A1):c.931G>A (p.Gly311Ser)
NM_001320537.2(SLC37A1):c.95A>G (p.Tyr32Cys) rs2517419031
NM_001320537.2(SLC37A1):c.985G>A (p.Val329Met)
NM_001320537.2(SLC37A1):c.990A>G (p.Ile330Met) rs2517579360

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