Variant #0000536311 (NC_000009.11:g.130478425A>G, NM_130459.3:c.*17070T>C (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.130478425A>G
DNA change (hg38) g.127716146A>G
Published as TTC16(NM_144965.3):c.1A>G (p.M1?)
ISCN -
DB-ID C9orf117_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) 0.00049 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-25 18:23:38 +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.-507T>C r.(?) p.(=)
C9orf117 NM_001012502.2 ?/. - c.*2241A>G r.(=) p.(=)
TOR2A NM_130459.3 ?/. - c.*17070T>C r.(=) p.(=)
TTC16 NM_144965.1 ?/. - c.1A>G r.(?) p.(Met1?)


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