Variant #0000403831 (NC_000010.10:g.112361870A>G, NM_005445.3:c.3039A>G (SMC3))
| Chromosome |
10 |
| Allele |
Parent #1 |
| 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.112361870A>G |
| DNA change (hg38) |
g.110602112A>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SMC3_000002 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs2419565 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.99685 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2009-09-05 15:31:35 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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