This variant has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Missense variant
Evidence status

Clinical significance

This variant has 5 synonyms - click the plus to show

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

About this variant

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

Variant displays