Variant #0000534864 (NC_000008.10:g.43002207G>A, NC_000008.10(NM_152419.2):c.234+1G>A (HGSNAT))
| Chromosome |
8 |
| Allele |
Unknown |
| 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.43002207G>A |
| DNA change (hg38) |
g.43147064G>A |
| Published as |
HGSNAT(NM_152419.2):c.234+1G>A |
| ISCN |
- |
| DB-ID |
HGSNAT_000007 See all 13 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
5.0E-5 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-06-23 19:19:18 +02:00 (CEST) |

Variant on transcripts
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