Variant #0000606366 (NC_000002.11:g.179312316_179312317insTGCAGGTTATGTCACCAACGGTTACTCTGAAGGTGAAAGTGGGCACGTGTATTTGCACATCAGATCTTTC, NC_000002.11(NM_003690.4):c.236-4_236-3insGAAAGATCTGATGTGCAAATACACGTGCCCACTTTCACCTTCAGAGTAACCGTTGGTGACATAACCTGCA (PRKRA))
| Chromosome |
2 |
| 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.179312316_179312317insTGCAGGTTATGTCACCAACGGTTACTCTGAAGGTGAAAGTGGGCACGTGTATTTGCACATCAGATCTTTC |
| DNA change (hg38) |
g.178447589_178447590insTGCAGGTTATGTCACCAACGGTTACTCTGAAGGTGAAAGTGGGCACGTGTATTTGCACATCAGATCTTTC |
| Published as |
PRKRA(NM_001139517.1):c.203-4_203-3insGAAAGATCTGATGTGCAAATACACGTGCCCACTTTCACCTTCAGAGTAACCGTTGGTGACATAACCTGCA (p.?) |
| ISCN |
- |
| DB-ID |
DFNB59_000026 |
| 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 14:54:23 +01:00 (CET) |
| Date last edited |
2020-06-09 19:35:27 +02:00 (CEST) |

Variant on transcripts
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