Variant #0000611523 (NC_000008.10:g.145583380C>T, NM_024531.4:c.228C>T (SLC52A2))
Chromosome |
8 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.145583380C>T |
DNA change (hg38) |
g.144359720C>T |
Published as |
SLC52A2(NM_024531.4):c.228C>T (p.D76=), SLC52A2(NM_024531.5):c.228C>T (p.D76=) |
ISCN |
- |
DB-ID |
SLC52A2_000015 See all 2 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) |
0.00073 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2019-12-04 15:24:38 +01:00 (CET) |
Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
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