Variant #0001041144 (NC_000016.9:g.46726435dup, NM_018206.4:c.-3390dup (VPS35))

Chromosome 16
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.46726435dup
DNA change (hg38) -
Published as ORC6(NM_014321.4):c.337dup (p.(Met113Asnfs*10))
ISCN -
DB-ID ORC6_000008
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
ORC6 NM_014321.3 +?/. - c.337dup r.(?) p.(Met113Asnfs*10)
VPS35 NM_018206.4 +?/. - c.-3390dup r.(?) p.(=)


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