Variant #0000566022 (NC_000019.9:g.11558370_11558372dup, NM_001001329.1:c.966_968dup (PRKCSH))
| Chromosome |
19 |
| 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.11558370_11558372dup |
| DNA change (hg38) |
g.11447555_11447557dup |
| Published as |
PRKCSH(NM_001289103.1):c.966_968dupGGA (p.E325dup), PRKCSH(NM_002743.3):c.966_968dupGGA (p.E325dup) |
| ISCN |
- |
| DB-ID |
ELAVL3_000005 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) |
Retrieve |
| 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 |
2024-10-29 21:08:56 +01:00 (CET) |

Variant on transcripts
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