Variant #0000931207 (NC_000020.10:g.62309621T>C, NM_016434.3:c.959T>C (RTEL1))
| Chromosome |
20 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.62309621T>C |
| DNA change (hg38) |
- |
| Published as |
RTEL1(NM_001283009.1):c.959T>C (p.M320T, p.(Met320Thr)), RTEL1(NM_001283010.1):c.290T>C (p.M97T), RTEL1(NM_032957.5):c.1031T>C (p.M344T) |
| ISCN |
- |
| DB-ID |
ARFRP1_000004 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) |
0.00115 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2023-07-07 10:10:56 +02:00 (CEST) |
| Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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