ClinVar Miner

List of variants in gene FGGY reported as uncertain significance for not specified

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Gene type:
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Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_018291.5(FGGY):c.614G>A (p.Ser205Asn) rs376744089 0.00019
NM_018291.5(FGGY):c.992A>G (p.Gln331Arg) rs149702935 0.00011
NM_018291.5(FGGY):c.285G>C (p.Gln95His) rs184449304 0.00009
NM_018291.5(FGGY):c.1565A>G (p.Gln522Arg) rs138656316 0.00006
NM_018291.5(FGGY):c.323A>G (p.His108Arg) rs201320585 0.00006
NM_018291.5(FGGY):c.911A>G (p.Lys304Arg) rs191411790 0.00006
NM_018291.5(FGGY):c.464A>G (p.Glu155Gly) rs754065271 0.00005
NM_018291.5(FGGY):c.68G>A (p.Arg23His) rs766518834 0.00005
NM_018291.5(FGGY):c.758C>T (p.Ala253Val) rs778888699 0.00004
NM_018291.5(FGGY):c.292C>A (p.Pro98Thr) rs370879908 0.00003
NM_018291.5(FGGY):c.463G>A (p.Glu155Lys) rs372475252 0.00003
NM_018291.5(FGGY):c.494C>T (p.Ala165Val) rs753319507 0.00003
NM_018291.5(FGGY):c.613A>T (p.Ser205Cys) rs371851463 0.00003
NM_018291.5(FGGY):c.526T>C (p.Ser176Pro) rs771642316 0.00002
NM_018291.5(FGGY):c.752G>A (p.Gly251Glu) rs753374977 0.00002
NM_018291.5(FGGY):c.863G>A (p.Arg288Gln) rs749366638 0.00002
NM_018291.5(FGGY):c.917C>T (p.Pro306Leu) rs768288661 0.00002
NM_018291.5(FGGY):c.925G>C (p.Val309Leu) rs761870388 0.00002
NM_018291.5(FGGY):c.1221+2938G>A rs1411513233 0.00001
NM_018291.5(FGGY):c.1222G>T (p.Val408Phe) rs762739100 0.00001
NM_018291.5(FGGY):c.1345A>G (p.Ile449Val) rs975746760 0.00001
NM_018291.5(FGGY):c.40G>A (p.Gly14Ser) rs1232063229 0.00001
NM_018291.5(FGGY):c.638A>G (p.Glu213Gly) rs748586572 0.00001
NM_018291.5(FGGY):c.710G>A (p.Gly237Glu) rs573781231 0.00001
NM_018291.5(FGGY):c.737T>C (p.Leu246Pro) rs1463439878 0.00001
NM_018291.5(FGGY):c.1076G>A (p.Cys359Tyr)
NM_018291.5(FGGY):c.1111G>C (p.Asp371His)
NM_018291.5(FGGY):c.113A>G (p.Asp38Gly) rs780674255
NM_018291.5(FGGY):c.1334C>G (p.Ala445Gly) rs564454743
NM_018291.5(FGGY):c.1346T>A (p.Ile449Asn) rs2535326079
NM_018291.5(FGGY):c.1369G>T (p.Gly457Cys)
NM_018291.5(FGGY):c.1436C>T (p.Ser479Leu)
NM_018291.5(FGGY):c.1510C>A (p.Gln504Lys)
NM_018291.5(FGGY):c.1516G>A (p.Ala506Thr) rs1271955991
NM_018291.5(FGGY):c.1619A>C (p.His540Pro) rs2537921847
NM_018291.5(FGGY):c.163T>C (p.Ser55Pro) rs1211776277
NM_018291.5(FGGY):c.166G>A (p.Glu56Lys)
NM_018291.5(FGGY):c.256A>G (p.Thr86Ala)
NM_018291.5(FGGY):c.283C>G (p.Gln95Glu) rs2050345969
NM_018291.5(FGGY):c.326G>A (p.Arg109Gln)
NM_018291.5(FGGY):c.413G>T (p.Gly138Val)
NM_018291.5(FGGY):c.41G>T (p.Gly14Val)
NM_018291.5(FGGY):c.548C>G (p.Thr183Arg) rs142640444
NM_018291.5(FGGY):c.609C>A (p.Asp203Glu)
NM_018291.5(FGGY):c.781G>A (p.Ala261Thr)
NM_018291.5(FGGY):c.782C>T (p.Ala261Val)
NM_018291.5(FGGY):c.829G>A (p.Gly277Ser) rs759042024
NM_018291.5(FGGY):c.838T>A (p.Cys280Ser)
NM_018291.5(FGGY):c.898A>T (p.Met300Leu) rs2530795867
NM_018291.5(FGGY):c.934G>A (p.Val312Ile)
NM_018291.5(FGGY):c.935T>C (p.Val312Ala)
NM_018291.5(FGGY):c.944C>T (p.Pro315Leu)
NM_018291.5(FGGY):c.997G>A (p.Val333Ile)

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