ZNF780B c.1727G>T ;(p.R576L)

Variant ID: 19-40541039-C-A

NM_001005851.2(ZNF780B):c.1727G>T;(p.R576L)

This variant was identified in 2 publications

View GRCh38 version.




Publications:


Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss.

Bmc Medical Genomics
Yang, Guangxian G; Yin, Yi Y; Tan, Zhiping Z; Liu, Jian J; Deng, Xicheng X; Yang, Yifeng Y
Publication Date: 2021-01-21

Variant appearance in text: rs61737024
PubMed Link: 33478437
Variant Present in the following documents:
  • 12920_2021_871_MOESM1_ESM.xls, sheet 1
View BVdb publication page



XomAnnotate: Analysis of Heterogeneous and Complex Exome- A Step towards Translational Medicine.

Plos One
Talukder, Asoke K AK; Ravishankar, Shashidhar S; Sasmal, Krittika K; Gandham, Santhosh S; Prabhukumar, Jyothsna J; Achutharao, Prahalad H PH; Barh, Debmalya D; Blasi, Francesco F
Publication Date: 2015

Variant appearance in text: rs61737024
PubMed Link: 25905921
Variant Present in the following documents:
  • pone.0123569.s008.xls, sheet 3
View BVdb publication page