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FAT1 c.9608A>G ;(p.D3203G)
Variant ID: 4-187532785-T-C
NM_005245.3(
FAT1
):c.9608A>G;(p.D3203G)
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:
NBN pathogenic germline variants are associated with pan-cancer susceptibility and in vitro DNA damage response defects.
Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Belhadj, Sami S; Khurram, Aliya A; Bandlamudi, Chaitanya C; Palou-Márquez, Guillermo G; Ravichandran, Vignesh V; Steinsnyder, Zoe Z; Wildman, Temima T; Catchings, Amanda A; Kemel, Yelena Y; Mukherjee, Semanti S; Fesko, Benjamin B; Arora, Kanika K; Mehine, Miika M; Dandiker, Sita S; Izhar, Aalin A; Petrini, John J; Domchek, Susan S; Nathanson, Katherine L KL; Brower, Jamie J; Couch, Fergus F; Stadler, Zsofia Z; Robson, Mark M; Walsh, Michael M; Vijai, Joseph J; Berger, Michael M; Supek, Fran F; Karam, Rachid R; Topka, Sabine S; Offit, Kenneth K
Publication Date: 2022-11-08
Variant appearance in text: FAT1: D3203G
PubMed Link:
36346689
Variant Present in the following documents:
ccr-22-1703_supplementary_tables_s1-s11_suppts1-ts11.xlsx, sheet 5
View BVdb publication page