Variant #0000568430 (NC_000019.9:g.55358743dup, NM_001242867.1:c.-3188dup (KIR3DL2))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.55358743dup
DNA change (hg38) g.54847288dup
Published as KIR2DS4(NM_012314.6):c.791_792insA (p.L265Pfs*30)
ISCN -
DB-ID KIR2DS4_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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.-3188dup r.(?) p.(=)
KIR2DS4 NM_012314.3 -/. - c.820dup r.(?) p.(Asn274LysfsTer21)


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