Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 9:99138006 (forward strand) | View in location tab

Co-located

with COSMIC COSM277669 (C/T) ; HGMD-PUBLIC CM061221

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB TGFBR1_722C_T_072211, 5764

This variant has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts, is associated with 3 phenotypes and is mentioned in 4 citations.

Variant displays