Variant #0000689686 (NC_000006.11:g.170871055del, TBP(NM_001172085.1):c.171del)
Chromosome |
6 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.170871055del |
DNA change (hg38) |
- |
Published as |
TBP(NM_003194.4):c.231_234delGCAGinsCAG (p.Q77Hfs*67), TBP(NM_003194.4):c.231_243delGCAGCAGCAGCAGinsCAGCAGCAGCAG (p.Q77Hfs*67), TBP(NM_003194.4):c.... |
ISCN |
- |
DB-ID |
TBP_000011 See all 3 reported entries |
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_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |

Variant on transcripts
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