Variant #0000318009 (NC_000009.11:g.130479998C>T, NM_130459.3:c.*15497G>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.130479998C>T
DNA change (hg38) g.127717719C>T
Published as TTC16(NM_144965.3):c.373C>T (p.Q125*)
ISCN -
DB-ID PTRH1_000001
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-25 18:24:03 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTRH1 NM_001002913.1 ?/. - c.-2080G>A r.(?) p.(=)
C9orf117 NM_001012502.2 ?/. - c.*3814C>T r.(=) p.(=)
TOR2A NM_130459.3 ?/. - c.*15497G>A r.(=) p.(=)
TTC16 NM_144965.1 ?/. - c.373C>T r.(?) p.(Gln125Ter)


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