Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [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
Evidence status

Clinical significance

Synonyms

LSDB TGFBR1_722C_T_072211, 5764

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

Variation displays