Variant #0000534203 (NC_000008.10:g.145583505C>A, NM_024531.4:c.353C>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.145583505C>A
DNA change (hg38) g.144359845C>A
Published as SLC52A2(NM_024531.4):c.353C>A (p.A118D), SLC52A2(NM_024531.5):c.353C>A (p.A118D)
ISCN -
DB-ID SLC52A2_000016 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) 0.00274 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM249 NM_001252402.1 -?/. - c.-5078G>T r.(?) p.(=)
SLC52A2 NM_024531.4 -?/. - c.353C>A r.(?) p.(Ala118Asp)
FBXL6 NM_024555.5 -?/. - c.-1398G>T r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.