Variant #0000666093 (NC_000012.11:g.98928103C>T, NM_003276.2:c.2068C>T (TMPO))
| Chromosome |
12 |
| Allele |
Both (homozygous) |
| 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.98928103C>T |
| DNA change (hg38) |
g.98534325C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TMPO_000051 See all 3 reported entries |
| Variant remarks |
allele frequency 0.015 ExAC database (February, 2017), identified in 141 homozygotes |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.01865 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2020-05-19 15:06:02 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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