Variant #0000000102 (NC_000011.10:g.64809858_64809861delAGAC, NM_000244.3:c.249_252delGTCT (MEN1))

Individual ID 00000004
Chromosome 11
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.64809858_64809861delAGAC
Published as -
Reference dbSNPB.T. Teh et al.(1998), dbSNP, ClinVar
DB-ID MEN1_000001
dbSNP ID rs587776841
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MyHVP
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by MyHVP
Date created 2017-11-22 09:33:14 +08:00 (CST)
Date last edited 2021-09-09 12:04:56 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
MEN1 NM_000244.3 +/. 2 c.249_252delGTCT - r.(?) p.(Ile85Serfs*33) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000017 DNA ? MEN1 1 MyHVP