Variant #0000349726 (NC_000008.10:g.145583745G>A, NM_024531.4:c.593G>A (SLC52A2))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.145583745G>A
DNA change (hg38) g.144360085G>A
Published as -
ISCN -
DB-ID SLC52A2_000009
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-24 19:07:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC52A2 NM_024531.4 +/. - c.593G>A r.(?) p.(Trp198Ter)
FBXL6 NM_024555.5 +/. - c.-1638C>T r.(?) p.(=)


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