Variant #0000534213 (NC_000008.10:g.145584497_145584499del, NM_024531.4:c.1160_1162del (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.145584497_145584499del
DNA change (hg38) g.144360837_144360839del
Published as SLC52A2(NM_024531.4):c.1160_1162delCCT (p.S387del)
ISCN -
DB-ID SLC52A2_000024
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC52A2 NM_024531.4 ?/. - c.1160_1162del r.(?) p.(Ser387del)
FBXL6 NM_024555.5 ?/. - c.-2390_-2388del r.(?) p.(=)


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