Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

C/G | Ambiguity code: S

Chromosome 20:63919816 (forward strand) | View in location tab


with COSMIC COSM3933913 (C/G)

Most severe consequence
Evidence status

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 2 individual genotypes and is mentioned in 1 citation.

Variation displays