Variant #0000933607 (NC_000013.10:g.100764317dup, NC_000013.10(NM_000282.3):c.300+2dup (PCCA))

Chromosome 13
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.100764317dup
DNA change (hg38) -
Published as -
ISCN -
DB-ID PCCA_000048
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2048370100
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-09-22 11:21:01 +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     
PCCA NM_000282.3 +?/. - c.300+2dup r.(?) p.(?)


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