Variant #0000990111 (NC_000001.10:g.11259709A>T, NM_004958.3:c.3996T>A (MTOR))

Chromosome 1
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.11259709A>T
DNA change (hg38) -
Published as MTOR(NM_004958.3):c.3996T>A (p.D1332E, p.(Asp1332Glu)), MTOR(NM_004958.4):c.3996T>A (p.D1332E)
ISCN -
DB-ID MTOR_000070 See all 3 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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MTOR NM_004958.3 -?/. - c.3996T>A r.(?) p.(Asp1332Glu)
ANGPTL7 NM_021146.2 -?/. - c.*4629A>T r.(=) p.(=)


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