Variant #0000283010 (NC_000019.9:g.40329748G>A, NM_004714.1:c.-5187C>T (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.40329748G>A
DNA change (hg38) g.39839108G>A
Published as FBL(NM_001436.4):c.476C>T (p.P159L)
ISCN -
DB-ID FBL_000002
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) 3.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FBL NM_001436.3 ?/. - c.476C>T r.(?) p.(Pro159Leu)
DYRK1B NM_004714.1 ?/. - c.-5187C>T r.(?) p.(=)


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