ClinVar Miner

List of variants in gene RASGRF1 studied for not specified

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Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_001145648.3(RASGRF1):c.812G>A (p.Arg271Gln) rs371901610 0.00007
NM_001145648.3(RASGRF1):c.3062A>T (p.His1021Leu) rs375185257 0.00005
NM_001145648.3(RASGRF1):c.1061G>A (p.Arg354His) rs778547354 0.00003
NM_001145648.3(RASGRF1):c.1616C>T (p.Ser539Phe) rs566305773 0.00003
NM_001145648.3(RASGRF1):c.1730G>A (p.Ser577Asn) rs774543725 0.00003
NM_001145648.3(RASGRF1):c.1783G>A (p.Ala595Thr) rs745650536 0.00003
NM_001145648.3(RASGRF1):c.2017G>A (p.Val673Met) rs370166186 0.00003
NM_001145648.3(RASGRF1):c.2659G>A (p.Ala887Thr) rs199661393 0.00003
NM_001145648.3(RASGRF1):c.3749G>A (p.Arg1250Gln) rs768043922 0.00003
NM_001145648.3(RASGRF1):c.856G>A (p.Val286Ile) rs766133238 0.00003
NM_001145648.3(RASGRF1):c.133G>A (p.Ala45Thr) rs760656612 0.00001
NM_001145648.3(RASGRF1):c.1760G>A (p.Arg587Gln) rs774275586 0.00001
NM_001145648.3(RASGRF1):c.2615C>G (p.Thr872Ser) rs975288968 0.00001
NM_001145648.3(RASGRF1):c.2654C>T (p.Ser885Leu) rs773604136 0.00001
NM_001145648.3(RASGRF1):c.2917G>A (p.Asp973Asn) rs779564323 0.00001
NM_001145648.3(RASGRF1):c.2962A>G (p.Ile988Val) rs776801006 0.00001
NM_001145648.3(RASGRF1):c.3737A>G (p.Glu1246Gly) rs551490924 0.00001
NM_001145648.3(RASGRF1):c.1069G>A (p.Asp357Asn)
NM_001145648.3(RASGRF1):c.1090G>A (p.Glu364Lys)
NM_001145648.3(RASGRF1):c.1196C>T (p.Thr399Met)
NM_001145648.3(RASGRF1):c.1273G>A (p.Asp425Asn)
NM_001145648.3(RASGRF1):c.1321C>T (p.Arg441Cys)
NM_001145648.3(RASGRF1):c.1357A>G (p.Thr453Ala)
NM_001145648.3(RASGRF1):c.1450C>G (p.Leu484Val) rs1219429381
NM_001145648.3(RASGRF1):c.1547G>C (p.Gly516Ala)
NM_001145648.3(RASGRF1):c.1636T>A (p.Leu546Met)
NM_001145648.3(RASGRF1):c.1834G>A (p.Ala612Thr)
NM_001145648.3(RASGRF1):c.2053C>T (p.Pro685Ser)
NM_001145648.3(RASGRF1):c.236C>A (p.Pro79His) rs1016058636
NM_001145648.3(RASGRF1):c.239A>G (p.Lys80Arg)
NM_001145648.3(RASGRF1):c.2497A>C (p.Ser833Arg)
NM_001145648.3(RASGRF1):c.251C>G (p.Ser84Trp) rs1223312169
NM_001145648.3(RASGRF1):c.2686G>A (p.Gly896Arg)
NM_001145648.3(RASGRF1):c.2716A>C (p.Lys906Gln)
NM_001145648.3(RASGRF1):c.2717A>C (p.Lys906Thr) rs2056477927
NM_001145648.3(RASGRF1):c.2827C>T (p.Arg943Cys) rs746752222
NM_001145648.3(RASGRF1):c.2933C>G (p.Thr978Ser)
NM_001145648.3(RASGRF1):c.2938G>A (p.Glu980Lys)
NM_001145648.3(RASGRF1):c.3001A>T (p.Ile1001Phe)
NM_001145648.3(RASGRF1):c.3010G>A (p.Glu1004Lys)
NM_001145648.3(RASGRF1):c.3020C>T (p.Thr1007Met)
NM_001145648.3(RASGRF1):c.3032A>C (p.Glu1011Ala)
NM_001145648.3(RASGRF1):c.3043G>A (p.Ala1015Thr)
NM_001145648.3(RASGRF1):c.3185A>G (p.Tyr1062Cys) rs2505422687
NM_001145648.3(RASGRF1):c.31C>A (p.His11Asn) rs2505819988
NM_001145648.3(RASGRF1):c.3637C>T (p.Arg1213Cys)
NM_001145648.3(RASGRF1):c.3655G>A (p.Ala1219Thr)
NM_001145648.3(RASGRF1):c.3675A>T (p.Gln1225His)
NM_001145648.3(RASGRF1):c.3682G>A (p.Val1228Ile)
NM_001145648.3(RASGRF1):c.3746T>A (p.Leu1249His) rs2505294425
NM_001145648.3(RASGRF1):c.571A>T (p.Thr191Ser)
NM_001145648.3(RASGRF1):c.589A>G (p.Asn197Asp) rs774664196
NM_001145648.3(RASGRF1):c.729G>C (p.Gln243His)
NM_001145648.3(RASGRF1):c.74G>A (p.Arg25His)

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