Variant #0000683397 (NC_000008.10:g.43025804C>A, HGSNAT(NM_152419.2):c.710C>A)

Individual ID 00307742
Chromosome 8
Allele Parent #2
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.43025804C>A
DNA change (hg38) g.43170661C>A
Published as -
ISCN -
DB-ID HGSNAT_000037 See all 8 reported entries
Variant remarks -
Reference PubMed: Grozeva 2015, Journal: Grozeva 2015
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HGSNAT NM_152419.2 +?/. - c.710C>A r.(?) p.(Pro237Gln)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000308882 DNA SEQ;SEQ-NG - 565 gene panel HGSNAT 2 Johan den Dunnen