Variant #0000567857 (NC_000019.9:g.47987230C>T, NM_007059.2:c.188G>A (KPTN))

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.47987230C>T
DNA change (hg38) g.47483973C>T
Published as KPTN(NM_007059.3):c.188G>A (p.R63Q)
ISCN -
DB-ID KPTN_000018
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) 0.00136 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
NAPA NM_003827.3 ?/. - c.*4315G>A r.(=) p.(=)
KPTN NM_007059.2 ?/. - c.188G>A r.(?) p.(Arg63Gln)


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