Variant #0000618203 (NC_000020.10:g.4893577_4893578insCGTA, NM_005116.5:c.155_156insTACG (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.4893577_4893578insCGTA
DNA change (hg38) g.4912931_4912932insCGTA
Published as SLC23A2(NM_005116.5):c.155_156insTACG (p.(Glu52AspfsTer5))
ISCN -
DB-ID SLC23A2_000008
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 14:56:19 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SLC23A2 NM_005116.5 -?/. - c.155_156insTACG r.(?) p.(Glu52AspfsTer5)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.