Variant #0000690205 (NC_000008.10:g.145577725G>A, NM_024531.4:c.-4829G>A (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.145577725G>A
DNA change (hg38) -
Published as TMEM249(NM_001280561.1):c.331C>T (p.R111C)
ISCN -
DB-ID SLC52A2_000037
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +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     
TMEM249 NM_001252402.1 ?/. - c.331C>T r.(?) p.(Arg111Cys)
SLC52A2 NM_024531.4 ?/. - c.-4829G>A r.(?) p.(=)
FBXL6 NM_024555.5 ?/. - c.*1466C>T r.(=) p.(=)


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