Variant #0000436511 (NC_000015.9:g.65369395C>T, NM_001101362.2:c.242C>T (KBTBD13))

Chromosome 15
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.65369395C>T
DNA change (hg38) g.65077057C>T
Published as -
ISCN -
DB-ID KBTBD13_000006 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2919358
Origin Germline
Segregation -
Frequency 0.31-0.50
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.44925 View details
Owner Johan den Dunnen
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 2012-11-02 20:42:42 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KBTBD13 NM_001101362.2 ?/. 1 c.242C>T r.(?) p.Ala81Val


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