Variant #0000050379 (NC_000006.11:g.86230111_86255652del, SNX14(NM_153816.3):c.1108+1181_2108-2342del)

Individual ID 00027202
Chromosome 6
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.86230111_86255652del
DNA change (hg38) g.85520393_85545934del
Published as -
ISCN -
DB-ID SNX14_000002 See all 4 reported entries
Variant remarks -
Reference PubMed: Thomas 2014
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Marianne Vos (LOVD-team)
Database submission license No license selected
Created by Marianne Vos (LOVD-team)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SNX14 NM_153816.3 +/. 12i_21i c.1108+1181_2108-2342del r.(del) p.(Glu370_Leu702del)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000027210 DNA arraySNP;SEQ - - SNX14 1 Marianne Vos (LOVD-team)