Variant #0000808863 (NC_000019.9:g.40327266T>G, NM_004714.1:c.-2705A>C (DYRK1B))

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.40327266T>G
DNA change (hg38) -
Published as FBL(NM_001436.4):c.725A>C (p.Q242P)
ISCN -
DB-ID DYRK1B_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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBL NM_001436.3 ?/. - c.725A>C r.(?) p.(Gln242Pro)
DYRK1B NM_004714.1 ?/. - c.-2705A>C r.(?) p.(=)


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