Variant #0000861125 (NC_000008.10:g.145582839T>C, NC_000008.10(NM_024531.4):c.-110-5T>C (SLC52A2))
Chromosome |
8 |
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.145582839T>C |
DNA change (hg38) |
- |
Published as |
SLC52A2(NM_024531.5):c.-110-5T>C |
ISCN |
- |
DB-ID |
SLC52A2_000056 |
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_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2022-05-09 15:51:19 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
|