Variant #0000341379 (NC_000019.9:g.47980074C>G, NM_007059.2:c.985G>C (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.47980074C>G
DNA change (hg38) g.47476817C>G
Published as KPTN(NM_007059.4):c.985G>C (p.A329P)
ISCN -
DB-ID KPTN_000010 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) 4.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +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.985G>C r.(?) p.(Ala329Pro)
SLC8A2 NM_015063.2 ?/. - c.-5045G>C r.(?) p.(=)


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