Variant #0000145977 (NC_000016.9:g.29567295_30226930del, NM_004608.3:c.-123785_*530251del (TBX6))
Chromosome |
16 |
Allele |
Parent #1 |
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.29567295_30226930del |
DNA change (hg38) |
g.29555974_30215609del |
Published as |
- |
ISCN |
- |
DB-ID |
TBX6_000006 |
Variant remarks |
NOTE: unclear whether breakpoint was sequenced or whether description represents the minimal or maximal extent of the deletion |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
yes |
Frequency |
5/94 cases |
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 07:43:58 +01:00 (CET) |
Date last edited |
2020-07-09 15:07:38 +02:00 (CEST) |

Variant on transcripts
Screenings
|