This variant has been flagged

Variation has more than 3 different alleles

Original source

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

A/C/G/T|Ancestral: A|Ambiguity code: N

Chromosome 14:73173663 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM004061, CM951070, CM951071

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 4 synonyms - Show

HGVS names

This variant has 66 HGVS names - Show

About this variant

This variant overlaps 66 transcripts, is associated with 5 phenotypes and is mentioned in 4 citations.

Variant displays