Variant #0000677796 (NC_000006.11:g.50791606_50791609dup, NC_000006.11(NM_003221.3):c.540+28_540+31dup (TFAP2B))
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.50791606_50791609dup |
DNA change (hg38) |
- |
Published as |
TFAP2B(NM_003221.3):c.540+7_540+10dup (p.(=)), TFAP2B(NM_003221.4):c.540+28_540+31dupCAAA |
ISCN |
- |
DB-ID |
TFAP2B_000001 See all 2 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_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2020-08-06 14:59:34 +02:00 (CEST) |
Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
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