This variation has been flagged

Variation has more than 3 different alleles

Original source

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

G/A/C/T | Ambiguity code: N

Chromosome X:71119403 (forward strand) | View in location tab


with COSMIC COSM131593 (G/T), COSM131594 (G/A), COSM131592 (G/C), COSM195151 (G/T), COSM145621 (G/A)

Most severe consequence
Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 24 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and is associated with 3 phenotypes.

Variation displays