Variant #0000611523 (NC_000008.10:g.145583380C>T, NM_024531.4:c.228C>T (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.145583380C>T
DNA change (hg38) g.144359720C>T
Published as SLC52A2(NM_024531.4):c.228C>T (p.D76=), SLC52A2(NM_024531.5):c.228C>T (p.D76=)
ISCN -
DB-ID SLC52A2_000015 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) 0.00073 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 2019-12-04 15:24:38 +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.-4953G>A r.(?) p.(=)
SLC52A2 NM_024531.4 -?/. - c.228C>T r.(?) p.(Asp76=)
FBXL6 NM_024555.5 -?/. - c.-1273G>A r.(?) p.(=)


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