Variant #0000806196 (NC_000013.10:g.51484284C>T, NC_000013.10(NM_024570.3):c.64+8C>T (RNASEH2B))
| Chromosome |
13 |
| 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.51484284C>T |
| DNA change (hg38) |
- |
| Published as |
RNASEH2B(NM_001142279.2):c.64+8C>T, RNASEH2B(NM_024570.3):c.64+8C>T |
| ISCN |
- |
| DB-ID |
RNASEH2B_000069 See all 2 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) |
0.00023 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2021-09-17 14:40:49 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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