Variant #0001002497 (NC_000016.9:g.685313G>A, NM_021168.4:c.*7691G>A (RAB40C))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.685313G>A
DNA change (hg38) -
Published as C16ORF13(NM_032366.3):c.388C>T (p.(Leu130Phe))
ISCN -
DB-ID RAB40C_000004
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) 0.0009 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C16orf13 NM_001040160.1 ?/. - c.388C>T r.(?) p.(Leu130Phe)
RAB40C NM_021168.4 ?/. - c.*7691G>A r.(=) p.(=)
WFIKKN1 NM_053284.2 ?/. - c.*1256G>A r.(=) p.(=)


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