Variant #0000912335 (NC_000005.9:g.37183719T>C, NM_023073.3:c.4564A>G (C5orf42))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.37183719T>C
DNA change (hg38) -
Published as CPLANE1(NM_023073.3):c.4564A>G (p.T1522A)
ISCN -
DB-ID C5orf42_000316
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) 1.0E-5 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 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C5orf42 NM_001384732.1 -?/. - c.4564A>G r.(?) p.(Thr1522Ala)
C5orf42 NM_023073.3 -?/. - c.4564A>G r.(?) p.(Thr1522Ala)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.