Variant #0000436514 (NC_000015.9:g.65370375C>T, NM_001101362.2:c.1222C>T (KBTBD13))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.65370375C>T
DNA change (hg38) g.65078037C>T
Published as -
ISCN -
DB-ID KBTBD13_000001 See all 5 reported entries
Variant remarks expression cloining inC2C12, mouse cardiomyocytes, no abnormalities obeserved
Reference PubMed: Sambuughin 2010, PubMed: Gommans 2003
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nyamkhishig Sambuughin
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2010-12-11 18:22:30 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KBTBD13 NM_001101362.2 -?/. 1 c.1222C>T r.(?) p.(Arg408Cys)


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