Original source

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

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

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

Co-located

with COSMIC COSM110581 (G/A) ; ESP TMP_ESP_6_161152796_161152796 (G/T)

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