Original source

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

Alleles
TTT/-
Location

Chromosome 14:102098480-102098482 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 1 sample genotype.

Variant displays