Variant #0000565241 (NC_000018.9:g.61018142_61018143insGATT, NM_002035.2:c.587_588insAATC (KDSR))

Chromosome 18
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.61018142_61018143insGATT
DNA change (hg38) g.63350909_63350910insGATT
Published as KDSR(NM_002035.4):c.587_588insAATC (p.A197Ifs*13)
ISCN -
DB-ID KDSR_000002
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 2020-07-15 09:00:27 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KDSR NM_002035.2 +/. - c.587_588insAATC r.(?) p.(Ala197IlefsTer13)


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