Variant #0000721853 (NC_000008.10:g.145583396C>T, NM_024531.4:c.244C>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.145583396C>T
DNA change (hg38) -
Published as SLC52A2(NM_001363118.1):c.244C>T (p.R82W), SLC52A2(NM_024531.5):c.244C>T (p.R82W)
ISCN -
DB-ID SLC52A2_000038 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) 7.0E-5 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM249 NM_001252402.1 ?/. - c.-4969G>A r.(?) p.(=)
SLC52A2 NM_024531.4 ?/. - c.244C>T r.(?) p.(Arg82Trp)
FBXL6 NM_024555.5 ?/. - c.-1289G>A r.(?) p.(=)


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