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

Alleles
T/A/C/G|Ancestral: T|Ambiguity code: N|MAF: 0.36 (G)
Location

Chromosome 12:12718165 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM033961

Most severe consequence
 
Missense variant
Evidence status

Synonyms

This variant has 5 synonyms - Show

HGVS names

This variant has 21 HGVS names - Show

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 15 transcripts, 1 regulatory feature, has 4141 sample genotypes and is mentioned in 26 citations.

Variant displays