Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 3:41224645 (forward strand) | View in location tab

Co-located

with COSMIC COSM5663 (T/C), COSM5685 (T/G), COSM5719 (T/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 6 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 and is associated with 3 phenotypes.

Variation displays