Original source

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

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

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

Co-located

with HGMD-PUBLIC CM092314, CM057649 ; PhenCode RettBASE_CDKL5:c.215T>A (T/A), RettBASE_CDKL5:c.215T>C (T/C)

Most severe consequence
Evidence status

Clinical significance

Synonyms

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

This variation has 18 HGVS names - click the plus to show

Variation displays