Variant #0000324502 (NC_000016.9:g.2522473_2522482del, NM_001199107.1:c.-2814_-2805del (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.2522473_2522482del
DNA change (hg38) g.2472472_2472481del
Published as NTN3(NM_006181.2):c.771_780del (p.(Cys257TrpfsTer13))
ISCN -
DB-ID NTN3_000009
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) 0.00174 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-09 11:07:18 +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.-2814_-2805del r.(?) p.(=)
NTN3 NM_006181.2 ?/. - c.771_780del r.(?) p.(Cys257TrpfsTer13)
TBC1D24 NM_020705.2 ?/. - c.-2814_-2805del r.(?) p.(=)
C16orf59 NM_025108.2 ?/. - c.*7804_*7813del r.(=) p.(=)


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