Variant #0000447003 (NC_000001.10:g.154164469A>C, NM_152263.3:c.(26T>G) (TPM3))
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic (dominant) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.154164469A>C |
| DNA change (hg38) |
g.154191993A>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TPM3_000001 See all 7 reported entries |
| Variant remarks |
mouse model; TPM2 decreased, alpha/beta heterodimer formation reduced |
| Reference |
PubMed: Corbett 2004, OMIM:var0001 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
animal model |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2008-09-22 10:14:28 +02:00 (CEST) |
| Date last edited |
2019-01-13 11:06:39 +01:00 (CET) |

Variant on transcripts
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