Variant #0000531776 (NC_000007.13:g.27239217C>T, NM_000522.4:c.480G>A (HOXA13))
| Chromosome |
7 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.27239217C>T |
| DNA change (hg38) |
g.27199598C>T |
| Published as |
HOXA13(NM_000522.5):c.480G>A (p.A160=) |
| ISCN |
- |
| DB-ID |
HOXA13_000007 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) |
0.00143 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-06-22 15:24:35 +02:00 (CEST) |

Variant on transcripts
|