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:31178784 (forward strand) | View in location tab

Co-located

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 7122, 2010_April_001_071_DMD_300377_0007

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

Variation displays