TF c.1583A>C ;(p.N528T)

Variant ID: 3-133486969-A-C

NM_001063.3(TF):c.1583A>C;(p.N528T)

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:

Polymorphism discovery and allele frequency estimation using high-throughput DNA sequencing of target-enriched pooled DNA samples.

Bmc Genomics
Mullen, Michael P MP; Creevey, Christopher J CJ; Berry, Donagh P DP; McCabe, Matt S MS; Magee, David A DA; Howard, Dawn J DJ; Killeen, Aideen P AP; Park, Stephen D SD; McGettigan, Paul A PA; Lucy, Matt C MC; Machugh, David E DE; Waters, Sinead M SM
Publication Date: 2012-01-11

Variant appearance in text: TF: N528T
PubMed Link: 22235840
Variant Present in the following documents:
  • Main text
View BVdb publication page