Variant #0000401466 (NC_000016.9:g.2546591G>A, NM_001199107.1:c.442G>A (TBC1D24))

Chromosome 16
Allele Paternal (confirmed)
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.2546591G>A
DNA change (hg38) g.2496590G>A
Published as -
ISCN -
DB-ID TBC1D24_000078
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Somatic
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner Jing Zhang
Database submission license No license selected
Created by Jing Zhang
Date created 2018-08-19 14:03:12 +02:00 (CEST)
Date last edited 2018-08-22 18:30:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBC1D24 NM_001199107.1 +?/. - c.442G>A r.(?) p.(Glu148Lys)
TBC1D24 NM_020705.2 +?/. - c.442G>A r.(?) p.(Glu148Lys)



Screenings

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