Variant #0007564762 (NC_000011.9:g.105948553C>T, NM_152433.3:c.-527G>A (KBTBD3))

Chromosome 11
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.105948553C>T
DB-ID -
dbSNP ID -
gnomAD frequency 1/246230
gnomAD homozygote count 0/123114
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AASDHPPT NM_015423.2 ./. c.116C>T r.(?) p.(Ser39Leu)
KBTBD3 NM_152433.3 ./. c.-527G>A r.(=) p.(=)
KBTBD3 NM_198439.2 ./. c.-728G>A r.(=) p.(=)