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TLN2 c.3521C>A ;(p.A1174D)
Variant ID: 15-63029239-C-A
NM_015059.2(
TLN2
):c.3521C>A;(p.A1174D)
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:
Genetic Diagnostic Yield and Novel Causal Genes of Congenital Heart Disease.
Frontiers In Genetics
Tan, Meihua M; Wang, Xinrui X; Liu, Hongjie H; Peng, Xiaoyan X; Yang, You Y; Yu, Haifei H; Xu, Liangpu L; Li, Jia J; Cao, Hua H
Publication Date: 2022
Variant appearance in text: TLN2: 3521C>A
PubMed Link:
35910219
Variant Present in the following documents:
DataSheet1.xlsx, sheet 7
View BVdb publication page