Variant #0000677272 (NC_000004.11:g.36345345C>A, NM_001170700.2:c.2245C>A (DTHD1))
| Chromosome |
4 |
| 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.36345345C>A |
| DNA change (hg38) |
- |
| Published as |
DTHD1(NM_001170700.2):c.2245C>A (p.R749S), DTHD1(NM_001170700.3):c.2620C>A (p.R874S) |
| ISCN |
- |
| DB-ID |
DTHD1_000007 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) |
0.00129 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2020-08-06 14:59:34 +02:00 (CEST) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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