Variant #0000931002 (NC_000019.9:g.12924157C>T, NM_006397.2:c.777C>T (RNASEH2A))
| Chromosome |
19 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.12924157C>T |
| DNA change (hg38) |
- |
| Published as |
RNASEH2A(NM_006397.2):c.777C>T (p.S259=), RNASEH2A(NM_006397.3):c.777C>T (p.S259=) |
| ISCN |
- |
| DB-ID |
RNASEH2A_000038 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) |
0.02937 View details |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2023-07-07 10:10:56 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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