Variant #0000323573 (NC_000014.8:g.23790699_23790701dup, NM_004643.3:c.21_23dup (PABPN1))

Chromosome 14
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.23790699_23790701dup
DNA change (hg38) g.23321490_23321492dup
Published as BCL2L2-PABPN1(NM_001199864.1):c.433-710_433-709insGGC (p.(=))
ISCN -
DB-ID PABPN1_000001 See all 15 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_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 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
BCL2L2-PABPN1 NM_001199864.1 ?/. - c.433-691_433-689dup - r.(=) p.(=)
BCL2L2 NM_004050.4 ?/. - c.*12525_*12527dup - r.(=) p.(=)
PABPN1 NM_004643.3 ?/. 1 c.21_23dup - r.(?) p.(Ala11dup)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.