Variant #0000436509 (NC_000015.9:g.65369951A>G, NM_001101362.2:c.798A>G (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.65369951A>G
DNA change (hg38) g.65077613A>G
Published as -
ISCN -
DB-ID KBTBD13_000004 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2919360
Origin Germline
Segregation -
Frequency 0.50-1.00
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.87368 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.798A>G r.(?) p.(=)


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