Variant #0000617864 (NC_000019.9:g.55327963T>G, NM_001080770.1:c.*2397T>G (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.55327963T>G
DNA change (hg38) g.54816508T>G
Published as KIR3DL1(NM_001322168.1):c.8T>G (p.L3R)
ISCN -
DB-ID KIR2DL4_000010
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIR2DL4 NM_001080770.1 ?/. - c.*2397T>G r.(=) p.(=)
KIR3DL1 NM_013289.2 ?/. - c.8T>G r.(?) p.(Leu3Arg)


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