Variant #0000332262 (NC_000008.10:g.101724627_101724628del, NM_002568.3:c.935_936del (PABPC1))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.101724627_101724628del
DNA change (hg38) g.100712399_100712400del
Published as PABPC1(NM_002568.3):c.935_936del (p.(Lys312ArgfsTer10))
ISCN -
DB-ID PABPC1_000006
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-24 15:09:16 +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.935_936del r.(?) p.(Lys312ArgfsTer10)


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