DNAH1 c.11788-52G>A

Variant ID: 3-52431671-G-A

NM_015512.4(DNAH1):c.11788-52G>A

This variant was identified in 6 publications

View GRCh38 version.




Publications:


Novel germline TRAF3IP3 mutation in a dyad with familial acute B lymphoblastic leukemia.

Cancer Reports (Hoboken, N.J.)
Pommert, Lauren L; Burns, Robert R; Furumo, Quinlan Q; Pulakanti, Kirthi K; Brandt, Jon J; Burke, Michael J MJ; Rao, Sridhar S
Publication Date: 2021-06

Variant appearance in text: DNAH1: 11788-52G>A; rs390802
PubMed Link: 33503336
Variant Present in the following documents:
  • CNR2-4-e1335-s003.xlsx, sheet 1
View BVdb publication page



MicroRNA-binding site polymorphisms and risk of colorectal cancer: A systematic review and meta-analysis.

Cancer Medicine
Gholami, Morteza M; Larijani, Bagher B; Sharifi, Farshad F; Hasani-Ranjbar, Shirin S; Taslimi, Reza R; Bastami, Milad M; Atlasi, Rasha R; Amoli, Mahsa M MM
Publication Date: 2019-12

Variant appearance in text: rs390802
PubMed Link: 31637880
Variant Present in the following documents:
  • Main text
  • CAM4-8-7477.pdf
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: DNAH1: 11788-52G>A; rs390802
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_7.xlsx, sheet 1
View BVdb publication page



Germline genetic variants in somatically significantly mutated genes in tumors are associated with renal cell carcinoma risk and outcome.

Carcinogenesis
Shu, Xiang X; Gu, Jianchun J; Huang, Maosheng M; Tannir, Nizar M NM; Matin, Surena F SF; Karam, Jose A JA; Wood, Christopher G CG; Wu, Xifeng X; Ye, Yuanqing Y
Publication Date: 2018-05-28

Variant appearance in text: rs390802
PubMed Link: 29635281
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common, germline genetic variations in the novel tumor suppressor BAP1 and risk of developing different types of cancer.

Oncotarget
Lin, Moubin M; Zhang, Liren L; Hildebrandt, Michelle A T MAT; Huang, Maosheng M; Wu, Xifeng X; Ye, Yuanqing Y
Publication Date: 2017-09-26

Variant appearance in text: rs390802
PubMed Link: 29088836
Variant Present in the following documents:
  • Main text
  • oncotarget-08-74936.pdf
View BVdb publication page



Identification of novel SNPs in glioblastoma using targeted resequencing.

Plos One
Keller, Andreas A; Harz, Christian C; Matzas, Mark M; Meder, Benjamin B; Katus, Hugo A HA; Ludwig, Nicole N; Fischer, Ulrike U; Meese, Eckart E
Publication Date: 2011

Variant appearance in text: rs390802
PubMed Link: 21695249
Variant Present in the following documents:
  • pone.0018158.s001.xls, sheet 5
  • pone.0018158.s001.xls, sheet 3
View BVdb publication page