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HEXA c.771T>A ;(p.F257L)
Variant ID: 15-72642893-A-T
NM_000520.4(
HEXA
):c.771T>A;(p.F257L)
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:
Identification of 12 cancer types through genome deep learning.
Scientific Reports
Sun, Yingshuai Y; Zhu, Sitao S; Ma, Kailong K; Liu, Weiqing W; Yue, Yao Y; Hu, Gang G; Lu, Huifang H; Chen, Wenbin W
Publication Date: 2019-11-21
Variant appearance in text: HEXA: F257L
PubMed Link:
31754222
Variant Present in the following documents:
41598_2019_53989_MOESM4_ESM.xlsx, sheet 8
View BVdb publication page