Variant #0000658662 (NC_000019.9:g.55363703G>A, NM_001242867.1:c.321G>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.55363703G>A
DNA change (hg38) g.54852248G>A
Published as KIR3DL2(NM_006737.3):c.321G>A (p.S107=)
ISCN -
DB-ID KIR2DS4_000007
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) 6.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2020-07-16 13:49:11 +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.321G>A r.(?) p.(Ser107=)
KIR2DS4 NM_012314.3 -?/. - c.*4305G>A r.(=) p.(=)


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