Variant #0000978129 (NC_000008.10:g.145584041G>T, NM_024531.4:c.889G>T (SLC52A2))
Chromosome |
8 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.145584041G>T |
DNA change (hg38) |
- |
Published as |
SLC52A2(NM_001363118.1):c.889G>T (p.V297L), SLC52A2(NM_001363118.2):c.889G>T (p.(Val297Leu)) |
ISCN |
- |
DB-ID |
SLC52A2_000039 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) |
5.0E-5 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2024-04-19 20:27:30 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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