Original source

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

T/C/G | Ancestral: T | Ambiguity code: B

Chromosome 3:41224621 (forward strand) | View in location tab


with COSMIC COSM5675 (T/G), COSM5687 (T/C), COSM5729 (T/A)

Most severe consequence

This variation has 3 synonyms - click the plus to show

This variation has 40 HGVS names - click the plus to show

About this variant

This variant overlaps 22 transcripts.

Variation displays