Variant #0000658862 (NC_000021.8:g.47754487_47754488insGGTGACCACCCACCAGAACAGCATGGGATGTTCACAGTC, PCNT(NM_006031.5):c.444_445insGGTGACCACCCACCAGAACAGCATGGGATGTTCACAGTC)

Chromosome 21
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.47754487_47754488insGGTGACCACCCACCAGAACAGCATGGGATGTTCACAGTC
DNA change (hg38) g.46334573_46334574insGGTGACCACCCACCAGAACAGCATGGGATGTTCACAGTC
Published as PCNT(NM_006031.6):c.444_445ins39 (p.V148_S149ins13)
ISCN -
DB-ID PCNT_000488
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) Variant not found in online data sets
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCNT NM_006031.5 -?/. - c.444_445insGGTGACCACCCACCAGAACAGCATGGGATGTTCACAGTC r.(?) p.(Val148_Ser149insGlyAspHisProProGluGlnHisGlyMetPheThrVal)