Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
CAGT/-
Location

Chromosome X:136167097-136167100 (forward strand) | View in location tab

Most severe consequence
 
Splice donor variant

This variant has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 22 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays