Variant #0000569925 (NC_000020.10:g.4893560_4893568del, NM_005116.5:c.166_174del (SLC23A2))

Chromosome 20
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.4893560_4893568del
DNA change (hg38) g.4912914_4912922del
Published as SLC23A2(NM_005116.5):c.166_174del (p.(Leu56_Ala58del))
ISCN -
DB-ID SLC23A2_000003
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
SLC23A2 NM_005116.5 -?/. - c.166_174del r.(?) p.(Leu56_Ala58del)


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