Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
T/A/C|Ancestral: T|Ambiguity code: H
Location

Chromosome X:18575423 (forward strand)|View in location tab

Co-located variants
Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB CDKL5: c.215T>A, CDKL5: c.215T>C, 6911

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and is associated with 5 phenotypes.

Variant displays