Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome X:31178784 (forward strand) | View in location tab


with COSMIC COSM3424730 (G/A), COSM3424728 (G/A), COSM3424729 (G/A), COSM3424733 (G/A), COSM3424732 (G/A), COSM3424731 (G/A) ; HGMD-PUBLIC CS921169, CM084898 ; PhenCode DMD:c.10108C>T (G/A)

Most severe consequence
Evidence status

Clinical significance


LSDB 7122, 2010_April_001_071_DMD_300377_0007

This variation has 35 HGVS names - click the plus to show

About this variant

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

Variation displays