Variant #0000866267 (NC_000019.9:g.55325299C>T, NM_001080770.1:c.762C>T (KIR2DL4))

Chromosome 19
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.55325299C>T
DNA change (hg38) -
Published as KIR2DL4(NM_002255.6):c.866C>T (p.A289V)
ISCN -
DB-ID KIR2DL4_000011
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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIR2DL4 NM_001080770.1 -?/. - c.762C>T r.(?) p.(Asp254=)
KIR3DL1 NM_013289.2 -?/. - c.-2657C>T r.(?) p.(=)


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