CALR c.137T>G ;(p.F46C)

Variant ID: 19-13049993-T-G

NM_004343.3(CALR):c.137T>G;(p.F46C)

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:

Misannotations of rRNA can now generate 90% false positive protein matches in metatranscriptomic studies.

Nucleic Acids Research
Tripp, H James HJ; Hewson, Ian I; Boyarsky, Sam S; Stuart, Joshua M JM; Zehr, Jonathan P JP
Publication Date: 2011-11-01

Variant appearance in text: CRT: F46C
PubMed Link: 21771858
Variant Present in the following documents:
  • supp_gkr576_StandardOperatingProcedures_Combined.pdf
View BVdb publication page