Variant #0000297028 (NC_000012.11:g.33049457C>A, NM_004572.3:c.209G>T (PKP2))
| Chromosome |
12 |
| 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.33049457C>A |
| DNA change (hg38) |
g.32896523C>A |
| Published as |
PKP2(NM_001005242.3):c.209G>T (p.(Ser70Ile)), PKP2(NM_004572.3):c.209G>T (p.S70I), PKP2(NM_004572.4):c.209G>T (p.S70I) |
| ISCN |
- |
| DB-ID |
PKP2_000011 See all 7 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) |
0.02121 View details |
| Owner |
VKGL-NL_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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