Most severe consequence
 
Frameshift variant
Alleles
T/-|Ancestral: T
Location

Chromosome 8:25423244 (forward strand)|View in location tab

Co-located variants

COSMIC COSM51077 ; HGMD-PUBLIC CD094315

Evidence status

Clinical significance

HGVS names

This variant has 9 HGVS names - Show

Synonyms

This variant has 2 synonyms - Show

Original source

Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP

About this variant

This variant overlaps 4 transcripts and is associated with 2 phenotypes.

Variant displays