Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome X:31206663 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM980563 ; PhenCode DMD:c.9568C>T (G/A)

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_081_DMD_300377_0076, 7191

HGVS names

This variant has 32 HGVS names - Show

About this variant

This variant overlaps 17 transcripts and is associated with 4 phenotypes.

Variant displays