Variant #0001040986 (NC_000016.9:g.2522475A>G, NM_001199107.1:c.-2812A>G (TBC1D24))

Chromosome 16
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.2522475A>G
DNA change (hg38) -
Published as NTN3(NM_006181.3):c.773A>G (p.(Asn258Ser))
ISCN -
DB-ID TBC1D24_000142
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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.-2812A>G r.(?) p.(=)
NTN3 NM_006181.2 ?/. - c.773A>G r.(?) p.(Asn258Ser)
TBC1D24 NM_020705.2 ?/. - c.-2812A>G r.(?) p.(=)
C16orf59 NM_025108.2 ?/. - c.*7806A>G r.(=) p.(=)


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