Variant #0000293966 (NC_000006.11:g.118880124_118880126del, PLN(NM_002667.3):c.40_42del)

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.118880124_118880126del
DNA change (hg38) g.118558961_118558963del
Published as PLN(NM_002667.3):c.40_42delAGA (p.R14del), PLN(NM_002667.5):c.40_42delAGA (p.R14del)
ISCN -
DB-ID PLN_000020 See all 7 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CEP85L NM_001042475.2 +/. - c.1020+6570_1020+6572del r.(=) p.(=)
PLN NM_002667.3 +/. - c.40_42del r.(?) p.(Arg14del)