Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome X:18600062 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM042955 ; PhenCode RettBASE_CDKL5:c.455G>T (G/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

Variation displays