Original source

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

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

Chromosome X:31178751 (forward strand) | View in location tab

Co-located

with COSMIC COSM1203827 (G/A), COSM1203828 (G/A), COSM1203829 (G/A), COSM1203825 (G/A), COSM1203824 (G/A), COSM1203826 (G/A) ; HGMD-PUBLIC CM930196 ; PhenCode DMD:c.10141C>T (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_078_DMD_300377_0067, 7182

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

Variation displays