Variant #0000610858 (NC_000007.13:g.129944340_129944347del, NM_016352.3:c.407_414del (CPA4))

Chromosome 7
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.129944340_129944347del
DNA change (hg38) g.130304500_130304507del
Published as CPA4(NM_001163446.1):c.306_313del (p.(Ile103ArgfsTer4))
ISCN -
DB-ID CPA4_000019
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-23 14:15:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPA4 NM_016352.3 ?/. - c.407_414del r.(?) p.(Ile136ArgfsTer4)


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