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
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