Variant #0000547919 (NC_000012.11:g.32994058A>C, NM_004572.3:c.1592T>G (PKP2))
| Chromosome |
12 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.32994058A>C |
| DNA change (hg38) |
g.32841124A>C |
| Published as |
PKP2(NM_001005242.2):c.1460T>G (p.(Ile487Ser)), PKP2(NM_004572.3):c.1592T>G (p.I531S), PKP2(NM_004572.4):c.1592T>G (p.I531S) |
| ISCN |
- |
| DB-ID |
PKP2_000056 See all 13 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) |
0.00493 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 |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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