Variant #0000655518 (NC_000006.11:g.15524698T>C, NC_000006.11(NM_032122.4):c.811+59A>G (DTNBP1))
Chromosome |
6 |
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.15524698T>C |
DNA change (hg38) |
g.15524467T>C |
Published as |
DTNBP1(NM_183040.2):c.870A>G (p.(Pro290=)) |
ISCN |
- |
DB-ID |
DTNBP1_000034 |
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) |
0.03594 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2020-03-23 16:13:27 +01:00 (CET) |
Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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