Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: < 0.01 (T)
Location

Chromosome 7:143351793 (forward strand)|View in location tab

Co-located variants

COSMIC COSM3635211 ; HGMD-PUBLIC CM004388

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 3 HGVS names - Hide

7:g.143351793C>T
ENST00000343257.6:c.2795C>T
ENSP00000339867.2:p.Pro932Leu

Genotyping chips

This variant has assays on: HumanCoreExome-12

About this variant

This variant overlaps 7 transcripts, has 2504 sample genotypes, is associated with 3 phenotypes and is mentioned in 1 citation.

Variant displays