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TET2 c.5666C>A ;(p.P1889H)
Variant ID: 4-106197333-C-A
NM_001127208.2(
TET2
):c.5666C>A;(p.P1889H)
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:
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: 5666C>A; P1889H
PubMed Link:
33252848
Variant Present in the following documents:
CTM2-10-e222-s003.xlsx, sheet 1
View BVdb publication page