Variant #0000016653 (NC_000008.10:g.94798513C>T, NM_153704.5:c.1351C>T (TMEM67))
| Chromosome |
8 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94798513C>T |
| DNA change (hg38) |
g.93786285C>T |
| Published as |
1351C>T: R451X |
| ISCN |
- |
| DB-ID |
TMEM67_000019 See all 6 reported entries |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs116647652 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0 View details |
| Owner |
Anne Polvi |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Anne Polvi |
| Date created |
2012-12-04 16:18:31 +01:00 (CET) |
| Date last edited |
2023-11-29 13:02:47 +01:00 (CET) |

Variant on transcripts
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