Variant #0000891687 (NC_000014.8:g.23790684_23790701dup, NM_004643.3:c.6_23dup (PABPN1))

Chromosome 14
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.23790684_23790701dup
DNA change (hg38) -
Published as PABPN1(NM_004643.3):c.6_23dupGGCGGCGGCGGCGGCGGC (p.A6_A11dup)
ISCN -
DB-ID PABPN1_000006 See all 6 reported entries
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 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
BCL2L2-PABPN1 NM_001199864.1 +?/. - c.433-706_433-689dup - r.(=) p.(=)
BCL2L2 NM_004050.4 +?/. - c.*12510_*12527dup - r.(=) p.(=)
PABPN1 NM_004643.3 +?/. - c.6_23dup - r.(?) p.(Ala6_Ala11dup)


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