SI c.1817C>T ;(p.T606I)

Variant ID: 3-164764699-G-A

NM_001041.3(SI):c.1817C>T;(p.T606I)

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:

A Case of Isolated Myeloid Sarcoma Associated With Germline EGFR T790M Variant: The Importance of Recognizing Potential Germline Variants on Somatic Tumor Sequencing Panels.

Journal Of Hematology
Walker, Margaret M; Folstad, Matthew M; Smith-Simmer, Kelcy K; Reinig, Erica E; Nadiminti, Kalyan K; Lovrien, Lauren L; Churpek, Jane E JE; Banaszak, Lauren G LG
Publication Date: 2022-04

Variant appearance in text: SI: 1817C>T; T606I
PubMed Link: 35573754
Variant Present in the following documents:
  • jh-11-071.pdf
View BVdb publication page