Variant #0000145981 (NC_000016.9:g.30102099C>A, NM_004608.3:c.333G>T (TBX6))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.30102099C>A |
| DNA change (hg38) |
g.30090778C>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TBX6_000002 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
yes |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Kazuki Takeda |
| Database submission license |
No license selected |
| Created by |
Kazuki Takeda |
| Date created |
2016-11-24 08:03:25 +01:00 (CET) |
| Date last edited |
2016-11-24 08:35:29 +01:00 (CET) |

Variant on transcripts
Screenings
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