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RET c.1903C>G ;(p.R635G)
Variant ID: 10-43609951-C-G
NM_020975.4(
RET
):c.1903C>G;(p.R635G)
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:
Usefulness of a novel device to divide core needle biopsy specimens in a spatially matched fashion.
Scientific Reports
Shiraishi, Takumi T; Inui, Shogo S; Inoue, Yuta Y; Saito, Yumiko Y; Taga, Hideto H; Kaneko, Masatomo M; Tsuji, Keisuke K; Ueda, Saya S; Ueda, Takashi T; Matsugasumi, Toru T; Taniguchi, Hidefumi H; Ueno, Akihisa A; Yamada, Takeshi T; Yamada, Yasuhiro Y; Iwata, Tsuyoshi T; Fujihara, Atsuko A; Hongo, Fumiya F; Ukimura, Osamu O
Publication Date: 2020-10-13
Variant appearance in text: rs377767410
PubMed Link:
33051506
Variant Present in the following documents:
41598_2020_74136_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page
Nine novel germline gene variants in the RET proto-oncogene identified in twelve unrelated cases.
The Journal Of Molecular Diagnostics : Jmd
Ahmed, Syed A SA; Snow-Bailey, Karen K; Highsmith, W Edward WE; Sun, Weimin W; Fenwick, Raymond G RG; Mao, Rong R
Publication Date: 2005-05
Variant appearance in text: MEN2A: R635G
PubMed Link:
15858153
Variant Present in the following documents:
Main text
View BVdb publication page