Variant #0000866613 (NC_000021.8:g.34100338C>T, NM_203446.2:c.14G>A (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.34100338C>T
DNA change (hg38) -
Published as SYNJ1(NM_203446.2):c.14G>A (p.W5*)
ISCN -
DB-ID PAXBP1_000003
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +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.*13482G>A r.(=) p.(=)
SYNJ1 NM_203446.2 +/. - c.14G>A r.(?) p.(Trp5*)


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