Original source

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

Alleles
G/A/T | Ambiguity code: D
Location

Chromosome 6:160731764 (forward strand) | View in location tab

Co-located

with COSMIC COSM110581 (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NC_000006.10:g.161072786G>A

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts, is associated with 1 phenotype and is mentioned in 1 citation.

Somatic mutation displays