Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Co-located variants
Most severe consequence
Synonymous variant
Evidence status

Clinical significance


LSDB NC_000006.10:g.161072786G>A

HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and is mentioned in 1 citation.

Somatic mutation displays