Variant #0000502499 (NC_000001.10:g.11253716G>A, NC_000001.10(NM_004958.3):c.4253+5599C>T (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.11253716G>A
DNA change (hg38) g.11193659G>A
Published as MTOR(NM_004958.4):c.4253+5599C>T
ISCN -
DB-ID MTOR_000047
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) 5.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.4253+5599C>T r.(=) p.(=)
ANGPTL7 NM_021146.2 -?/. - c.557G>A r.(?) p.(Arg186Gln)


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