Variant #0000610905 (NC_000007.13:g.149419571_149419572insGCC, NM_032534.2:c.525_526insGCC (KRBA1))
| 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.149419571_149419572insGCC |
| DNA change (hg38) |
g.149722480_149722481insGCC |
| Published as |
KRBA1(NM_032534.2):c.525_526insGCC (p.(Glu175_Pro176insAla)) |
| ISCN |
- |
| DB-ID |
KRBA1_000006 |
| 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_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2020-06-23 14:46:32 +02:00 (CEST) |

Variant on transcripts
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