TG c.1002del ;(p.C336Afs*66)

Variant ID: 8-133895168-AG-A

NM_003235.4(TG):c.1002del;(p.C336Afs*66)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Newborn Screening and Molecular Profile of Congenital Hypothyroidism in a Chinese Population.

Frontiers In Genetics
Yu, Bin B; Long, Wei W; Yang, Yuqi Y; Wang, Ying Y; Jiang, Lihua L; Cai, Zhengmao Z; Wang, Huaiyan H
Publication Date: 2018

Variant appearance in text: TG: 1000delG
PubMed Link: 30420871
Variant Present in the following documents:
  • Main text
  • fgene-09-00509.pdf
View BVdb publication page