Variant #0000978130 (NC_000008.10:g.145584361G>A, NM_024531.4:c.1113G>A (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.145584361G>A
DNA change (hg38) -
Published as SLC52A2(NM_001253815.1):c.1113G>A (p.(Gly371=)), SLC52A2(NM_001363118.2):c.1113G>A (p.G371=), SLC52A2(NM_024531.4):c.1113G>A (p.G371=), SLC52A2(NM...)
ISCN -
DB-ID SLC52A2_000023 See all 4 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) 0.00013 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-04-19 20:27:30 +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.1113G>A r.(?) p.(Gly371=)
FBXL6 NM_024555.5 -?/. - c.-2254C>T r.(?) p.(=)


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