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PCTP c.29A>T ;(p.E10V)
Variant ID: 17-53828493-A-T
NM_021213.3(
PCTP
):c.29A>T;(p.E10V)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Highly diversified core promoters in the human genome and their effects on gene expression and disease predisposition.
Bmc Genomics
Gupta, Hemant H; Chandratre, Khyati K; Sinha, Siddharth S; Huang, Teng T; Wu, Xiaobing X; Cui, Jian J; Zhang, Michael Q MQ; Wang, San Ming SM
Publication Date: 2020-11-30
Variant appearance in text: rs12941739
PubMed Link:
33256598
Variant Present in the following documents:
12864_2020_7222_MOESM2_ESM.xlsx, sheet 3
12864_2020_7222_MOESM2_ESM.xlsx, sheet 20
12864_2020_7222_MOESM2_ESM.xlsx, sheet 2
12864_2020_7222_MOESM2_ESM.xlsx, sheet 17
View BVdb publication page
Genome-wide SNP typing reveals signatures of population history.
Genomics
Hughes, Austin L AL; Welch, Robert R; Puri, Vinita V; Matthews, Casey C; Haque, Kashif K; Chanock, Stephen J SJ; Yeager, Meredith M
Publication Date: 2008-07
Variant appearance in text: rs12941739
PubMed Link:
18485661
Variant Present in the following documents:
Main text
View BVdb publication page