Variant #0000223357 (NC_000008.10:g.14095199T>C, NC_000008.10(NM_139167.2):c.337-11A>G (SGCZ))
| Chromosome |
8 |
| Allele |
Parent #1 |
| 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.14095199T>C |
| DNA change (hg38) |
g.14237690T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SGCZ_000004 See all 2 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs28658359 |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
0.26 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.26399 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2008-02-23 18:19:01 +01:00 (CET) |
| Date last edited |
2012-11-02 20:43:05 +01:00 (CET) |

Variant on transcripts
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