Variant #0000997495 (NC_000009.11:g.130491894C>T, NM_130459.3:c.*3601G>A (TOR2A))

Chromosome 9
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.130491894C>T
DNA change (hg38) -
Published as TTC16(NM_144965.1):c.1799C>T (p.(Ala600Val))
ISCN -
DB-ID C9orf117_000002
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) 2.0E-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 2024-08-28 13:16:32 +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     
PTRH1 NM_001002913.1 ?/. - c.-13976G>A r.(?) p.(=)
C9orf117 NM_001012502.2 ?/. - c.*15710C>T r.(=) p.(=)
TOR2A NM_130459.3 ?/. - c.*3601G>A r.(=) p.(=)
TTC16 NM_144965.1 ?/. - c.1799C>T r.(?) p.(Ala600Val)


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