ClinVar Miner

List of variants in gene GOLGA1

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Total variants: 71
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HGVS dbSNP gnomAD frequency
NM_002077.4(GOLGA1):c.1806T>G (p.Thr602=) rs16927704 0.00420
NM_002077.4(GOLGA1):c.1497+8C>G rs201455650 0.00115
NM_002077.4(GOLGA1):c.191A>G (p.Asn64Ser) rs148050398 0.00031
NM_002077.4(GOLGA1):c.916A>G (p.Arg306Gly) rs774101149 0.00031
NM_002077.4(GOLGA1):c.1019C>T (p.Ala340Val) rs138783087 0.00024
NM_002077.4(GOLGA1):c.2287C>T (p.Arg763Trp) rs143825735 0.00024
NM_002077.4(GOLGA1):c.1144A>G (p.Thr382Ala) rs150137668 0.00023
NM_002077.4(GOLGA1):c.1366C>T (p.Arg456Cys) rs145802446 0.00019
NM_002077.4(GOLGA1):c.2000G>A (p.Arg667Gln) rs138765093 0.00018
NM_002077.4(GOLGA1):c.220C>A (p.Leu74Ile) rs145566855 0.00017
NM_002077.4(GOLGA1):c.2035C>T (p.Pro679Ser) rs145763272 0.00015
NM_002077.4(GOLGA1):c.1163C>T (p.Ala388Val) rs201106148 0.00013
NM_002077.4(GOLGA1):c.1641C>T (p.Ala547=) rs199534446 0.00013
NM_002077.4(GOLGA1):c.1555G>A (p.Glu519Lys) rs200756008 0.00010
NM_002077.4(GOLGA1):c.1415G>T (p.Trp472Leu) rs150023063 0.00009
NM_002077.4(GOLGA1):c.559A>C (p.Met187Leu) rs755795939 0.00009
NM_002077.4(GOLGA1):c.844G>T (p.Val282Phe) rs148532217 0.00006
NM_002077.4(GOLGA1):c.1552A>G (p.Thr518Ala) rs1048803619 0.00005
NM_002077.4(GOLGA1):c.2255A>G (p.Lys752Arg) rs748185454 0.00005
NM_002077.4(GOLGA1):c.1544G>A (p.Arg515Gln) rs774959189 0.00004
NM_002077.4(GOLGA1):c.1406A>C (p.Lys469Thr) rs761042816 0.00002
NM_002077.4(GOLGA1):c.2021T>C (p.Met674Thr) rs769477508 0.00002
NM_002077.4(GOLGA1):c.1036G>A (p.Ala346Thr) rs752034801 0.00001
NM_002077.4(GOLGA1):c.202C>T (p.Arg68Trp) rs763271118 0.00001
NM_002077.4(GOLGA1):c.2237G>C (p.Gly746Ala) rs1025595839 0.00001
NM_002077.4(GOLGA1):c.31G>A (p.Glu11Lys) rs755588954 0.00001
NM_002077.4(GOLGA1):c.764A>C (p.Glu255Ala) rs1413424575 0.00001
NM_002077.4(GOLGA1):c.1009C>G (p.Gln337Glu)
NM_002077.4(GOLGA1):c.1064G>A (p.Arg355Gln)
NM_002077.4(GOLGA1):c.1108C>A (p.Leu370Ile)
NM_002077.4(GOLGA1):c.1116G>C (p.Gln372His)
NM_002077.4(GOLGA1):c.1132G>A (p.Ala378Thr)
NM_002077.4(GOLGA1):c.118G>A (p.Asp40Asn) rs2491051871
NM_002077.4(GOLGA1):c.1232G>A (p.Arg411His)
NM_002077.4(GOLGA1):c.1241C>T (p.Ala414Val)
NM_002077.4(GOLGA1):c.1283C>G (p.Ala428Gly)
NM_002077.4(GOLGA1):c.1287C>A (p.Asp429Glu) rs1288450905
NM_002077.4(GOLGA1):c.1361A>G (p.Tyr454Cys)
NM_002077.4(GOLGA1):c.142G>A (p.Asp48Asn)
NM_002077.4(GOLGA1):c.1469G>A (p.Arg490Gln)
NM_002077.4(GOLGA1):c.1478G>A (p.Arg493Lys)
NM_002077.4(GOLGA1):c.1514C>A (p.Ala505Asp)
NM_002077.4(GOLGA1):c.1525G>A (p.Glu509Lys)
NM_002077.4(GOLGA1):c.1553C>A (p.Thr518Asn)
NM_002077.4(GOLGA1):c.155C>G (p.Ser52Cys)
NM_002077.4(GOLGA1):c.1598G>A (p.Arg533Gln)
NM_002077.4(GOLGA1):c.1607A>G (p.Asn536Ser) rs372990641
NM_002077.4(GOLGA1):c.1627C>A (p.His543Asn)
NM_002077.4(GOLGA1):c.1644G>C (p.Glu548Asp)
NM_002077.4(GOLGA1):c.1648G>C (p.Glu550Gln) rs2490815872
NM_002077.4(GOLGA1):c.1681G>A (p.Ala561Thr)
NM_002077.4(GOLGA1):c.1718G>A (p.Arg573Gln)
NM_002077.4(GOLGA1):c.1734C>T (p.Ala578=) rs34090990
NM_002077.4(GOLGA1):c.1757C>T (p.Ser586Leu)
NM_002077.4(GOLGA1):c.1778T>C (p.Met593Thr)
NM_002077.4(GOLGA1):c.1863G>C (p.Lys621Asn) rs1023316762
NM_002077.4(GOLGA1):c.2020A>T (p.Met674Leu)
NM_002077.4(GOLGA1):c.2187G>C (p.Glu729Asp)
NM_002077.4(GOLGA1):c.2299T>C (p.Ser767Pro)
NM_002077.4(GOLGA1):c.241G>T (p.Val81Phe)
NM_002077.4(GOLGA1):c.305C>T (p.Ser102Phe) rs1830710034
NM_002077.4(GOLGA1):c.443T>C (p.Ile148Thr)
NM_002077.4(GOLGA1):c.475C>G (p.Gln159Glu) rs749413063
NM_002077.4(GOLGA1):c.490T>C (p.Phe164Leu)
NM_002077.4(GOLGA1):c.640G>A (p.Glu214Lys) rs1269251175
NM_002077.4(GOLGA1):c.701A>G (p.Gln234Arg)
NM_002077.4(GOLGA1):c.716C>T (p.Thr239Met)
NM_002077.4(GOLGA1):c.796C>A (p.Gln266Lys)
NM_002077.4(GOLGA1):c.829A>G (p.Ile277Val)
NM_002077.4(GOLGA1):c.919C>A (p.Leu307Ile)
NM_002077.4(GOLGA1):c.941A>G (p.Glu314Gly)

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