Variant #0000595601 (NC_000008.10:g.43013853A>T, HGSNAT(NM_152419.2):c.370A>T)
Individual ID |
00263909 |
Chromosome |
8 |
Allele |
Both (homozygous) |
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.43013853A>T |
DNA change (hg38) |
g.43158710A>T |
Published as |
- |
ISCN |
- |
DB-ID |
HGSNAT_000124 See all 4 reported entries |
Variant remarks |
- |
Reference |
PubMed: Haer-Wigman 2015 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
yes |
Frequency |
- |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
Owner |
Johan den Dunnen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |

Variant on transcripts
Screenings
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