Variant #0001035222 (NC_000005.9:g.37226614C>T, NM_023073.3:c.2083G>A (C5orf42))

Chromosome 5
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.37226614C>T
DNA change (hg38) -
Published as CPLANE1(NM_001384732.1):c.2083G>A (p.(Val695Ile))
ISCN -
DB-ID C5orf42_000348
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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C5orf42 NM_001384732.1 ?/. - c.2083G>A r.(?) p.(Val695Ile)
C5orf42 NM_023073.3 ?/. - c.2083G>A r.(?) p.(Val695Ile)


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