Variant #0000401462 (NC_000016.9:g.2546265C>T, NM_001199107.1:c.116C>T (TBC1D24))

Chromosome 16
Allele Maternal (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.2546265C>T
DNA change (hg38) g.2496264C>T
Published as -
ISCN -
DB-ID TBC1D24_000070 See all 7 reported entries
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 13:53:31 +02:00 (CEST)
Date last edited 2018-08-20 16:45:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBC1D24 NM_001199107.1 +?/. - c.116C>T r.(?) p.(Ala39Val)
TBC1D24 NM_020705.2 +?/. - c.116C>T r.(?) p.(Ala39Val)



Screenings

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