Canonical Allele Identifier: CA4455799
Gene: WNT16 HGNC NCBI
COSMIC:
COSM3762343 (not active)
COSM3762344 (not active)
MyVariant.info:
GRCh38 chr7:g.121339035C>T
GRCh37 chr7:g.120979089C>T
Revel Score:
ENST00000361301 0.099
ENST00000222462 (MANE Select) 0.099
gnomAD v2:
7:120979089 C / T
gnomAD v3:
7:121339035 C / T
gnomAD v4:
chr7-121339035-C-T
Joint Max Group AF 0.8295498 (AFR)
Genomes Max Group AF 0.81886349 (AFR)
Exomes Max Group AF 0.8377475 (AFR)
dbSNP:
2707466
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.121339035C>T , CM000669.2:g.121339035C>T GRCh38
NC_000007.13:g.120979089C>T , CM000669.1:g.120979089C>T GRCh37
NC_000007.12:g.120766325C>T NCBI36
NG_029242.1:g.18669C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000222462.3:c.788C>T MANE Select ENSP00000222462.2:p.Thr263Ile
ENST00000222462.2:c.788C>T ENSP00000222462.2:p.Thr263Ile
ENST00000361301.6:c.758C>T ENSP00000355065.2:p.Thr253Ile
NM_016087.2:c.758C>T NP_057171.2:p.Thr253Ile
NM_057168.1:c.788C>T NP_476509.1:p.Thr263Ile
NM_057168.2:c.788C>T MANE Select NP_476509.1:p.Thr263Ile
Search 100 bp 5'
Search 100 bp 3'