Variant #0000247895 (NC_000001.10:g.20977000A>C, PINK1(NM_032409.2):c.1562A>C)
Chromosome |
1 |
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.20977000A>C |
DNA change (hg38) |
g.20650507A>C |
Published as |
PINK1(NM_032409.2):c.1562A>C (p.N521T), PINK1(NM_032409.3):c.1562A>C (p.N521T) |
ISCN |
- |
DB-ID |
PINK1_000062 See all 5 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) |
0.29304 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |

Variant on transcripts
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