Variant #0000017973 (NC_000001.10:g.89847539T>C, NC_000001.10(NM_198460.2):c.1152+6T>C (GBP6))
| Chromosome |
1 |
| Allele |
Both (homozygous) |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.89847539T>C |
| DNA change (hg38) |
g.89381980T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
GBP6_000001 |
| Variant remarks |
variant marked as interesting (probably affects the function of the gene with phenotypic consequences) from an exome analysis. Please contact me. |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
1 |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00183 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2013-05-06 10:12:12 +02:00 (CEST) |
| Date last edited |
2014-10-05 12:34:31 +02:00 (CEST) |

Variant on transcripts
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