Variant #0000859925 (NC_000005.9:g.37205466G>A, NM_023073.3:c.3240C>T (C5orf42))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.37205466G>A
DNA change (hg38) -
Published as CPLANE1(NM_023073.3):c.3240C>T (p.A1080=)
ISCN -
DB-ID C5orf42_000304
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) 0.00311 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C5orf42 NM_001384732.1 -/. - c.3240C>T r.(?) p.(Ala1080=)
C5orf42 NM_023073.3 -/. - c.3240C>T r.(?) p.(Ala1080=)


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