Variant #0000536312 (NC_000009.11:g.130493404G>A, NM_130459.3:c.*2091C>T (TOR2A))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.130493404G>A
DNA change (hg38) g.127731125G>A
Published as TTC16(NM_144965.3):c.2342G>A (p.R781Q)
ISCN -
DB-ID TOR2A_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) 9.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TOR2A NM_130459.3 -?/. - c.*2091C>T r.(=) p.(=)
TTC16 NM_144965.1 -?/. - c.2342G>A r.(?) p.(Arg781Gln)


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