Variant #0000272319 (NC_000005.9:g.37226961G>A, NM_023073.3:c.1736C>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.37226961G>A
DNA change (hg38) g.37226859G>A
Published as C5orf42(NM_023073.3):c.1736C>T (p.A579V), CPLANE1(NM_001384732.1):c.1736C>T (p.(Ala579Val)), CPLANE1(NM_023073.4):c.1736C>T (p.A579V)
ISCN -
DB-ID C5orf42_000116 See all 4 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) 0.00126 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C5orf42 NM_023073.3 -/. - c.1736C>T r.(?) p.(Ala579Val)


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