Variant #0000326798 (NC_000019.9:g.55329851A>G, NM_001080770.1:c.*4285A>G (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.55329851A>G
DNA change (hg38) g.54818396A>G
Published as KIR3DL1(NM_013289.2):c.152A>G (p.(Tyr51Cys))
ISCN -
DB-ID KIR3DL1_000003
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) 0.00858 View details
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 2024-08-28 13:16:32 +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.*4285A>G r.(=) p.(=)
KIR3DL1 NM_013289.2 -?/. - c.152A>G r.(?) p.(Tyr51Cys)


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