Original source

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

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

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

Co-located

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

Most severe consequence

This variation has 3 synonyms - click the plus to show

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

Variation displays