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Home / Genome / All Variants / BRCA1 c.181T>G — reference vs missense variant

Variant

BRCA1 c.181T>G — reference vs missense variant

c.181T>G · p.Cys61Gly · NC_000017.10:g.41258504A>C

Findlay: LOF ClinVar: Pathogenic

Reference (A)

Alternate (B)

Educational demonstration

Personal research and education tool — not for clinical diagnosis. Findlay 2018 SGE LOF missense (41586_2018_461_MOESM3_ESM.xlsx); ClinVar VCV000017661 Pathogenic. GRCh37 750 bp window centered on hg19 41258504.