Variant #0001075687 (NC_000008.10:g.68334861C>T, NM_020361.4:c.1192G>A (CPA6))

Chromosome 8
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.68334861C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID CPA6_000074
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs775233588
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-04-29 10:42:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPA6 NM_020361.4 ?/. - c.1192G>A r.(?) p.(Glu398Lys)


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