ClinVar Miner

List of variants in gene GP6 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 30
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HGVS dbSNP gnomAD frequency
NM_016363.5(GP6):c.655C>T (p.Pro219Ser) rs1613662 0.83313
NM_016363.5(GP6):c.964A>C (p.Asn322His) rs1671152 0.81180
NM_016363.5(GP6):c.950T>A (p.Leu317Gln) rs1654413 0.80050
NM_016363.5(GP6):c.495T>C (p.Phe165=) rs892089 0.75735
NM_016363.5(GP6):c.*792T>C rs1671150 0.75248
NM_016363.5(GP6):c.*395C>T rs1671151 0.74102
NM_016363.5(GP6):c.*693A>G rs1654412 0.74079
NM_016363.5(GP6):c.745G>A (p.Ala249Thr) rs2304167 0.73790
NM_016363.5(GP6):c.936C>G (p.Leu312=) rs2304166 0.48243
NM_016363.5(GP6):c.507G>A (p.Thr169=) rs5030705 0.14894
NM_016363.5(GP6):c.*703G>A rs10418074 0.06591
NM_016363.5(GP6):c.*471G>A rs41275822 0.02358
NM_016363.5(GP6):c.*781C>T rs2886416 0.01283
NM_016363.5(GP6):c.*263G>A rs74697203 0.01200
NM_016363.5(GP6):c.35-19C>T rs189534942 0.00848
NM_016363.5(GP6):c.*728_*729insTCCC rs761185718 0.00644
NM_016363.5(GP6):c.307C>G (p.Leu103Val) rs28969501 0.00283
NM_016363.5(GP6):c.881G>A (p.Arg294Gln) rs201997410 0.00147
NM_016363.5(GP6):c.*599G>A rs368531531 0.00008
NM_016363.5(GP6):c.*170TCTG[5] rs768134535
NM_016363.5(GP6):c.*371T>G
NM_016363.5(GP6):c.*692C>T
NM_016363.5(GP6):c.*782G>A
NM_016363.5(GP6):c.390A>T (p.Val130=)
NM_016363.5(GP6):c.484A>C (p.Arg162=) rs892090
NM_016363.5(GP6):c.576A>G (p.Ser192=) rs1654425
NM_016363.5(GP6):c.60G>A (p.Ala20=)
NM_016363.5(GP6):c.709G>A (p.Glu237Lys) rs1654416
NM_016363.5(GP6):c.72G>A (p.Pro24=)
NM_016363.5(GP6):c.932CCCTCCCGC[1] (p.308PLP[2])

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