Variant #0000550740 (NC_000013.10:g.37427813C>G, NC_000013.10(NM_001127217.2):c.1004-1G>C (SMAD9))
| Chromosome |
13 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.37427813C>G |
| DNA change (hg38) |
g.36853676C>G |
| Published as |
SMAD9(NM_001127217.2):c.1004-1G>C |
| ISCN |
- |
| DB-ID |
SMAD9_000008 |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-07-03 16:26:45 +02:00 (CEST) |

Variant on transcripts
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