Variant #0000533327 (NC_000008.10:g.101719035_101719115del, NC_000008.10(NM_002568.3):c.1447+1_1448-1del (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.101719035_101719115del
DNA change (hg38) g.100706807_100706887del
Published as PABPC1(NM_002568.3):c.1447+1_1448-1del (p.?)
ISCN -
DB-ID PABPC1_000007
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-24 15:09:15 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PABPC1 NM_002568.3 -?/. - c.1447+1_1448-1del r.spl? p.?


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