Variant #0000655381 (NC_000005.9:g.37227868A>C, NM_023073.3:c.1173T>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.37227868A>C
DNA change (hg38) g.37227766A>C
Published as CPLANE1(NM_023073.3):c.1173T>G (p.A391=), CPLANE1(NM_023073.4):c.1173T>G (p.A391=)
ISCN -
DB-ID C5orf42_000122 See all 2 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) 0.0006 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C5orf42 NM_023073.3 -?/. - c.1173T>G r.(?) p.(Ala391=)


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