Variant #0000716689 (NC_000001.10:g.11259668G>A, NM_004958.3:c.4037C>T (MTOR))

Chromosome 1
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.11259668G>A
DNA change (hg38) -
Published as MTOR(NM_004958.4):c.4037C>T (p.T1346I)
ISCN -
DB-ID MTOR_000049
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MTOR NM_004958.3 ?/. - c.4037C>T r.(?) p.(Thr1346Ile)
ANGPTL7 NM_021146.2 ?/. - c.*4588G>A r.(=) p.(=)


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