Variant #0000948558 (NC_000005.9:g.37244554del, NM_023073.3:c.493del (C5orf42))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.37244554del
DNA change (hg38) -
Published as C5orf42(NM_023073.3):c.493del (p.(Ile165TyrfsTer17))
ISCN -
DB-ID C5orf42_000012 See all 6 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) 0.00015 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 2023-11-27 17:35:39 +01:00 (CET)
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.493del r.(?) p.(Ile165Tyrfs*17)
C5orf42 NM_023073.3 +?/. - c.493del r.(?) p.(Ile165Tyrfs*17)


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