Original source

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

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

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

Co-located

with 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

This variant has 32 HGVS names - click the plus to show

About this variant

This variant overlaps 17 transcripts and is associated with 3 phenotypes.

Variant displays