Variant #0000860665 (NC_000007.13:g.139715542C>G, NM_001061.4:c.1249C>G (TBXAS1))
| Chromosome |
7 |
| 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.139715542C>G |
| DNA change (hg38) |
- |
| Published as |
TBXAS1(NM_001061.4):c.1249C>G (p.(Gln417Glu)), TBXAS1(NM_001061.7):c.1246C>G (p.Q416E) |
| ISCN |
- |
| DB-ID |
TBXAS1_000023 See all 4 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) |
0.00211 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2022-05-09 15:51:19 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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