Variant #0000311976 (NC_000009.11:g.132576387C>A, NM_000113.2:c.863G>T (TOR1A))

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.132576387C>A
DNA change (hg38) g.129814108C>A
Published as TOR1A(NM_000113.3):c.863G>T (p.R288L)
ISCN -
DB-ID TOR1A_000012 See all 2 reported entries
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TOR1A NM_000113.2 ?/. - c.863G>T r.(?) p.(Arg288Leu)
TOR1B NM_014506.1 ?/. - c.*4525C>A r.(=) p.(=)


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