Variant #0001052464 (NC_000006.11:g.111136248G>A, NM_015076.3:c.92C>T (CDK19))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.111136248G>A
DNA change (hg38) -
Published as CDK19(NM_015076.5):c.92C>T (p.(Thr31Ile))
ISCN -
DB-ID AMD1_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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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     
AMD1 NM_001033059.1 +?/. - c.-60188G>A r.(?) p.(=)
CDK19 NM_015076.3 +?/. - c.92C>T r.(?) p.(Thr31Ile)


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