Variant #0000996834 (NC_000008.10:g.101725047_101725048dup, NC_000008.10(NM_002568.3):c.739-21_739-20dup (PABPC1))

Chromosome 8
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.101725047_101725048dup
DNA change (hg38) -
Published as PABPC1(NM_002568.4):c.739-21_739-20dupTT
ISCN -
DB-ID PABPC1_000017
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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     
PABPC1 NM_002568.3 -?/. - c.739-21_739-20dup r.(=) p.(=)


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