Original source

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

A/C | Ancestral: A | Ambiguity code: M

Chromosome 7:94427801 (forward strand) | View in location tab


with HGMD-PUBLIC CM962768

Most severe consequence
Missense variant
Evidence status


This variant has 2 synonyms - Show

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, has 2 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays