Variant #0000807296 (NC_000016.9:g.2546606G>A, NM_001199107.1:c.457G>A (TBC1D24))

Chromosome 16
Allele Unknown
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.2546606G>A
DNA change (hg38) -
Published as TBC1D24(NM_001199107.1):c.457G>A (p.E153K, p.(Glu153Lys))
ISCN -
DB-ID TBC1D24_000096 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 7.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBC1D24 NM_001199107.1 +?/. - c.457G>A r.(?) p.(Glu153Lys)
TBC1D24 NM_020705.2 +?/. - c.457G>A r.(?) p.(Glu153Lys)


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