Variant #0001035426 (NC_000006.11:g.118786602G>T, NM_002667.3:c.-83051G>T (PLN))

Chromosome 6
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.118786602G>T
DNA change (hg38) -
Published as CEP85L(NM_001042475.3):c.2384C>A (p.A795D)
ISCN -
DB-ID PLN_000075
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CEP85L NM_001042475.2 ?/. - c.2384C>A r.(?) p.(Ala795Asp)
PLN NM_002667.3 ?/. - c.-83051G>T r.(?) p.(=)


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