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CD36 c.702_703insGTAA ;(p.N235Vfs*14)
Variant ID: 7-80295759-G-GGTAA
NM_001001548.2(
CD36
):c.702_703insGTAA;(p.N235Vfs*14)
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:
Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss.
Plos One
Bakhchane, Amina A; Charif, Majida M; Bousfiha, Amale A; Boulouiz, Redouane R; Nahili, Halima H; Rouba, Hassan H; Charoute, Hicham H; Lenaers, Guy G; Barakat, Abdelhamid A
Publication Date: 2017
Variant appearance in text: CD36: 702_703insGTAA
PubMed Link:
28472130
Variant Present in the following documents:
pone.0176516.s002.xlsx, sheet 1
View BVdb publication page