Variant #0000912398 (NC_000006.11:g.118880118dup, PLN(NM_002667.3):c.34dup)

Chromosome 6
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.118880118dup
DNA change (hg38) -
Published as PLN(NM_002667.5):c.34dupA (p.I12Nfs*8)
ISCN -
DB-ID PLN_000062
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 2023-01-11 15:44:22 +01:00 (CET)
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.1020+6574dup r.(=) p.(=)
PLN NM_002667.3 +?/. - c.34dup r.(?) p.(Ile12Asnfs*8)