Variant #0000326802 (NC_000019.9:g.55363674T>A, NM_001242867.1:c.292T>A (KIR3DL2))

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.55363674T>A
DNA change (hg38) g.54852219T>A
Published as KIR3DL2(NM_001242867.1):c.292T>A (p.(Ser98Thr))
ISCN -
DB-ID KIR3DL2_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) 0.00055 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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIR3DL2 NM_001242867.1 -?/. - c.292T>A r.(?) p.(Ser98Thr)
KIR2DS4 NM_012314.3 -?/. - c.*4276T>A r.(=) p.(=)


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