Variant #0000277649 (NC_000008.10:g.43014192G>A, NC_000008.10(NM_152419.2):c.493+5G>A (HGSNAT))
| Chromosome |
8 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.43014192G>A |
| DNA change (hg38) |
g.43159049G>A |
| Published as |
HGSNAT(NM_001363227.2):c.493+5G>A, HGSNAT(NM_152419.3):c.493+5G>A |
| ISCN |
- |
| DB-ID |
HGSNAT_000060 See all 4 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) |
2.0E-5 View details |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2024-10-29 21:08:56 +01:00 (CET) |

Variant on transcripts
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