Variant #0000618326 (NC_000021.8:g.34099164dup, NM_203446.2:c.164dup (SYNJ1))

Chromosome 21
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.34099164dup
DNA change (hg38) g.32726853dup
Published as -
ISCN -
DB-ID SYNJ1_000062
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-16 22:04:15 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAXBP1 NM_013329.3 +/. - c.*14660dup r.(?) p.(=)
SYNJ1 NM_203446.2 +/. - c.164dup r.(?) p.(Pro56ThrfsTer9)


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