Variant #0001036846 (NC_000008.10:g.145584087T>C, NM_024531.4:c.935T>C (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.145584087T>C
DNA change (hg38) -
Published as SLC52A2(NM_001363118.2):c.935T>C (p.(Leu312Pro))
ISCN -
DB-ID SLC52A2_000054 See all 3 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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC52A2 NM_024531.4 +/. - c.935T>C r.(?) p.(Leu312Pro)
FBXL6 NM_024555.5 +/. - c.-1980A>G r.(?) p.(=)


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