Variant #0000995294 (NC_000006.11:g.118786654G>A, NM_002667.3:c.-82999G>A (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.118786654G>A
DNA change (hg38) -
Published as CEP85L(NM_001042475.2):c.2332C>T (p.(Gln778*))
ISCN -
DB-ID PLN_000065
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 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     
CEP85L NM_001042475.2 ?/. - c.2332C>T r.(?) p.(Gln778*)
PLN NM_002667.3 ?/. - c.-82999G>A r.(?) p.(=)


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