CALR c.35_36insG ;(p.G13Rfs*47)

Variant ID: 19-13049528-T-TG

NM_004343.3(CALR):c.35_36insG;(p.G13Rfs*47)

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:

Common genes for non-syndromic deafness are uncommon in sub-Saharan Africa: a report from Nigeria.

International Journal Of Pediatric Otorhinolaryngology
Lasisi, Akeem O AO; Bademci, Guney G; Foster, Joseph J; Blanton, Susan S; Tekin, Mustafa M
Publication Date: 2014-11

Variant appearance in text: SSA: 35insG
PubMed Link: 25218342
Variant Present in the following documents:
  • Main text
View BVdb publication page