Original source

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

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

Chromosome 17:39715897 (forward strand)|View in location tab

Co-located variants
Most severe consequence
Stop gained
Evidence status

Clinical significance


LSDB NC_000017.9:g.35125676C>T

HGVS names

This variant has 56 HGVS names - Show

About this variant

This variant overlaps 42 transcripts and is mentioned in 1 citation.

Somatic mutation displays