Variant #0000326405 (NC_000019.9:g.38572753_38572772dup, NM_015073.1:c.548_567dup (SIPA1L3))

Chromosome 19
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.38572753_38572772dup
DNA change (hg38) g.38082113_38082132dup
Published as SIPA1L3(NM_015073.1):c.545_546insGGACGCGGGGGAGCCGCGGG (p.(Ala190ThrfsTer40))
ISCN -
DB-ID SIPA1L3_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 2020-07-15 17:44:06 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SIPA1L3 NM_015073.1 ?/. - c.548_567dup r.(?) p.(Ala190ThrfsTer40)


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