Original source

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

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

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

Co-located variants

COSMIC COSM277669 ; HGMD-PUBLIC CM061221

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB TGFBR1_722C_T_072211, 5764

HGVS names

This variant has 13 HGVS names - Show

About this variant

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

Variant displays