F2 c.19_20delinsCC ;(p.L7P)

Variant ID: 11-46740804-TT-CC

NM_000506.3(F2):c.19_20delinsCC;(p.L7P)

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:

Identification of genes influencing skeletal phenotypes in congenic P/NP rats.

Journal Of Bone And Mineral Research : The Official Journal Of The American Society For Bone And Mineral Research
Alam, Imranul I; Carr, Lucinda G LG; Liang, Tiebing T; Liu, Yunlong Y; Edenberg, Howard J HJ; Econs, Michael J MJ; Turner, Charles H CH
Publication Date: 2010-06

Variant appearance in text: F2: Leu7Pro
PubMed Link: 20200994
Variant Present in the following documents:
  • Main text
  • jbmr0025-1314.pdf
View BVdb publication page