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NOTCH1 c.7496_7497insTCC ;(p.S2499_H2500insP)
Variant ID: 9-139390694-G-GGGA
NM_017617.3(
NOTCH1
):c.7496_7497insTCC;(p.S2499_H2500insP)
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:
Acquired somatic variants in inherited myeloid malignancies.
Leukemia
Armes, Hannah H; Rio-Machin, Ana A; Krizsán, Szilvia S; Bödör, Csaba C; Kaya, Fadimana F; Bewicke-Copley, Findlay F; Alnajar, Jenna J; Walne, Amanda A; Péterffy, Borbála B; Tummala, Hemanth H; Rouault-Pierre, Kevin K; Dokal, Inderjeet I; Vulliamy, Tom T; Fitzgibbon, Jude J
Publication Date: 2022-05
Variant appearance in text: NOTCH1: 7496_7497insTCC
PubMed Link:
35140362
Variant Present in the following documents:
41375_2022_1515_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page