Variant #0000595574 (NC_000008.10:g.43025320_43027867delinsAGAATATG, HGSNAT(NM_152419.2):c.634-408_820+338delinsAGAATATG)

Individual ID 00263888
Chromosome 8
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.43025320_43027867delinsAGAATATG
DNA change (hg38) g.43170177_43172724delinsAGAATATG
Published as -
ISCN -
DB-ID HGSNAT_000123
Variant remarks -
Reference PubMed: Van Cauwenbergh 2016
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HGSNAT NM_152419.2 +/. 6i_8i c.634-408_820+338delinsAGAATATG r.(634_820del) p.(Glu212Glyfs*2)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000264999 DNA SEQ;SEQ-NG - RP gene panel HGSNAT 2 Johan den Dunnen