Variant #0000948612 (NC_000006.11:g.111136257C>T, NM_015076.3:c.83G>A (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.111136257C>T
DNA change (hg38) -
Published as CDK19(NM_001300960.2):c.83G>A (p.G28E)
ISCN -
DB-ID AMD1_000001
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-11-27 17:35:39 +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.-60179C>T r.(?) p.(=)
CDK19 NM_015076.3 +?/. - c.83G>A r.(?) p.(Gly28Glu)


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