Variant #0000531947 (NC_000007.13:g.40085606A>G, NM_003718.4:c.2525A>G (CDK13))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.40085606A>G
DNA change (hg38) g.40046007A>G
Published as CDK13(NM_003718.4):c.2525A>G (p.(Asn842Ser), p.N842S), CDK13(NM_003718.5):c.2525A>G (p.N842S)
ISCN -
DB-ID CDK13_000005 See all 5 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) 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDK13 NM_003718.4 +/. - c.2525A>G r.(?) p.(Asn842Ser)


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