Variant #0000653589 (NC_000001.10:g.11316244C>G, NM_004958.3:c.510G>C (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.11316244C>G
DNA change (hg38) g.11256187C>G
Published as MTOR(NM_004958.3):c.510G>C (p.L170=), MTOR(NM_004958.4):c.510G>C (p.L170=)
ISCN -
DB-ID MTOR_000086 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) 0.00338 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 2020-03-23 16:13:27 +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.510G>C r.(?) p.(Leu170=)


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