Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.01 (A)
Location

Chromosome 7:140015845 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM054133

Most severe consequence
 
Missense variant
Evidence status

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 19 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 10 transcripts and has 3399 sample genotypes.

Variant displays