Variant #0000983960 (NC_000021.8:g.34100261T>A, NM_203446.2:c.91A>T (SYNJ1))

Chromosome 21
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.34100261T>A
DNA change (hg38) -
Published as SYNJ1(NM_003895.3):c.91A>T (p.(Lys31*))
ISCN -
DB-ID PAXBP1_000004
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAXBP1 NM_013329.3 ?/. - c.*13559A>T r.(=) p.(=)
SYNJ1 NM_203446.2 ?/. - c.91A>T r.(?) p.(Lys31*)


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