Variant #0000970280 (NC_000021.8:g.34099201C>T, NM_203446.2:c.123G>A (SYNJ1))

Chromosome 21
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.34099201C>T
DNA change (hg38) -
Published as SYNJ1(NM_003895.3):c.123G>A (p.A41=), SYNJ1(NM_203446.2):c.123G>A (p.A41=)
ISCN -
DB-ID SYNJ1_000001 See all 2 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) 0.00512 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAXBP1 NM_013329.3 -?/. - c.*14619G>A r.(=) p.(=)
SYNJ1 NM_203446.2 -?/. - c.123G>A r.(?) p.(=)


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