Variant #0000802463 (NC_000006.11:g.28227439A>G, NM_001007531.1:c.290A>G (NKAPL))

Chromosome 6
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.28227439A>G
DNA change (hg38) -
Published as NKAPL(NM_001007531.2):c.290A>G (p.H97R)
ISCN -
DB-ID NKAPL_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) 1.0E-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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NKAPL NM_001007531.1 -?/. - c.290A>G r.(?) p.(His97Arg)
ZKSCAN4 NM_019110.3 -?/. - c.-7681T>C r.(?) p.(=)


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