Variant #0000326795 (NC_000019.9:g.55325364_55325365del, NM_001080770.1:c.827_828del (KIR2DL4))

Chromosome 19
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.55325364_55325365del
DNA change (hg38) g.54813909_54813910del
Published as KIR2DL4(NM_001080770.1):c.824_825del (p.?)
ISCN -
DB-ID KIR2DL4_000005
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-16 13:47:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIR2DL4 NM_001080770.1 ?/. - c.827_828del r.(?) p.(Arg276LysfsTer26)
KIR3DL1 NM_013289.2 ?/. - c.-2592_-2591del r.(?) p.(=)


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