Variant #0001046539 (NC_000016.9:g.2090177A>T, NM_002528.7:c.748T>A (NTHL1))
| Chromosome |
16 |
| 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.2090177A>T |
| DNA change (hg38) |
g.2040176A>T |
| Published as |
NTHL1(NM_001318193.1):c.601T>A (p.(Ser201Thr)) |
| ISCN |
- |
| DB-ID |
NTHL1_000050 |
| 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) |
7.0E-5 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2025-07-08 13:22:38 +02:00 (CEST) |
| Date last edited |
2025-11-01 10:49:15 +01:00 (CET) |

Variant on transcripts
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