Variant #0000567852 (NC_000019.9:g.47978735G>A, NM_007059.2:c.1249C>T (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.47978735G>A
DNA change (hg38) g.47475478G>A
Published as KPTN(NM_007059.3):c.1249C>T (p.R417C), KPTN(NM_007059.4):c.1249C>T (p.R417C)
ISCN -
DB-ID KPTN_000013 See all 2 reported entries
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) 0.00011 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KPTN NM_007059.2 ?/. - c.1249C>T r.(?) p.(Arg417Cys)
SLC8A2 NM_015063.2 ?/. - c.-3706C>T r.(?) p.(=)


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