Variant #0000316479 (NC_000006.11:g.10404782G>C, NM_003220.2:c.723C>G (TFAP2A))
| 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.10404782G>C |
| DNA change (hg38) |
g.10404549G>C |
| Published as |
TFAP2A(NM_001032280.2):c.705C>G (p.P235=) |
| ISCN |
- |
| DB-ID |
TFAP2A_000013 |
| 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) |
9.0E-5 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2020-06-18 14:24:16 +02:00 (CEST) |

Variant on transcripts
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