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TET2 c.5698G>C ;(p.V1900L)
Variant ID: 4-106197365-G-C
NM_001127208.2(
TET2
):c.5698G>C;(p.V1900L)
This variant was identified in 3 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
A sex-informed approach to improve the personalised decision making process in myelodysplastic syndromes: a multicentre, observational cohort study.
The Lancet. Haematology
,
Publication Date: 2022-11-24
Variant appearance in text: TET2: 5698G>C; V1900L
PubMed Link:
36436542
Variant Present in the following documents:
mmc2.xlsx, sheet 1
View BVdb publication page
Comprehensive next-generation profiling of clonal hematopoiesis in cancer patients using paired tumor-blood sequencing for guiding personalized therapies.
Clinical And Translational Medicine
Li, Ziyang Z; Huang, Wensou W; Yin, Jiani C JC; Na, Chenglong C; Wu, Xue X; Shao, Yang Y; Ding, Huaxin H; Li, Jinming J
Publication Date: 2020-11
Variant appearance in text: TET2: 5698G>C; V1900L
PubMed Link:
33252848
Variant Present in the following documents:
CTM2-10-e222-s003.xlsx, sheet 1
View BVdb publication page
Invariant patterns of clonal succession determine specific clinical features of myelodysplastic syndromes.
Nature Communications
Nagata, Yasunobu Y; Makishima, Hideki H; Kerr, Cassandra M CM; Przychodzen, Bartlomiej P BP; Aly, Mai M; Goyal, Abhinav A; Awada, Hassan H; Asad, Mohammad Fahad MF; Kuzmanovic, Teodora T; Suzuki, Hiromichi H; Yoshizato, Tetsuichi T; Yoshida, Kenichi K; Chiba, Kenichi K; Tanaka, Hiroko H; Shiraishi, Yuichi Y; Miyano, Satoru S; Mukherjee, Sudipto S; LaFramboise, Thomas T; Nazha, Aziz A; Sekeres, Mikkael A MA; Radivoyevitch, Tomas T; Haferlach, Torsten T; Ogawa, Seishi S; Maciejewski, Jaroslaw P JP
Publication Date: 2019-11-26
Variant appearance in text: TET2: V1900L
PubMed Link:
31772163
Variant Present in the following documents:
41467_2019_13001_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page