ClinVar Miner

List of variants in gene FANCG reported as likely benign for DNA repair disease

Included ClinVar conditions (95):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NM_004629.1(FANCG):c.-504A>T rs17885140
NM_004629.1(FANCG):c.1017T>C (p.His339=) rs764465471
NM_004629.1(FANCG):c.1365C>A (p.Thr455=) rs767385265
NM_004629.1(FANCG):c.1433+9G>A rs187315404
NM_004629.1(FANCG):c.1545C>T (p.Ala515=) rs201422773
NM_004629.1(FANCG):c.1578C>T (p.Ala526=) rs1060504371
NM_004629.1(FANCG):c.1767C>T (p.Leu589=) rs1060504369
NM_004629.1(FANCG):c.177G>A (p.Gly59=) rs1554670511
NM_004629.1(FANCG):c.1806C>T (p.Pro602=) rs756632525
NM_004629.1(FANCG):c.333G>A (p.Gly111=) rs1060504370
NM_004629.1(FANCG):c.345A>G (p.Glu115=) rs1213271836
NM_004629.1(FANCG):c.366G>C (p.Trp122Cys) rs546023787
NM_004629.1(FANCG):c.373_375dupGTC (p.Val125_Leu126insVal) rs750843326
NM_004629.1(FANCG):c.375C>A (p.Val125=) rs199754122
NM_004629.1(FANCG):c.399G>A (p.Pro133=) rs200278002
NM_004629.1(FANCG):c.558C>G (p.Pro186=) rs1554670415
NM_004629.1(FANCG):c.705G>A (p.Ala235=) rs148910563
NM_004629.1(FANCG):c.722C>T (p.Pro241Leu) rs201438531
NM_004629.1(FANCG):c.739C>A (p.Gln247Lys) rs145613634
NM_004629.1(FANCG):c.81C>T (p.Ala27=) rs1060504372
NM_004629.1(FANCG):c.927C>G (p.Ala309=) rs370002843

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