Variant #0000618202 (NC_000020.10:g.4893576_4893577insG, NM_005116.5:c.156_157insC (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.4893576_4893577insG
DNA change (hg38) g.4912930_4912931insG
Published as SLC23A2(NM_005116.5):c.156_157insC (p.(Asp53ArgfsTer3))
ISCN -
DB-ID SLC23A2_000007
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-16 14:56:18 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC23A2 NM_005116.5 -?/. - c.156_157insC r.(?) p.(Asp53ArgfsTer3)


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