Original source

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

G/A/T | Ancestral: G | Ambiguity code: D

Chromosome 3:41224613 (forward strand) | View in location tab


with COSMIC COSM5671 (G/A), COSM5670 (G/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 7 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, is associated with 4 phenotypes and is mentioned in 1 citation.

Variation displays