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

Chromosome 10:124397951 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM920532

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 4 synonyms - Show

HGVS names

This variant has 24 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 15 transcripts, has 2 sample genotypes, is associated with 4 phenotypes and is mentioned in 1 citation.

Variant displays