Variant #0000270561 (NC_000008.10:g.68396042C>T, NM_020361.4:c.799G>A (CPA6))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.68396042C>T
DNA change (hg38) g.67483807C>T
Published as CPA6(NM_020361.4):c.799G>A (p.G267R), CPA6(NM_020361.5):c.799G>A (p.G267R)
ISCN -
DB-ID CPA6_000002 See all 9 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) 0.00203 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
CPA6 NM_020361.4 +?/. - c.799G>A r.(?) p.(Gly267Arg)


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