Variant #0000993877 (NC_000003.11:g.66023892G>A, NM_004742.2:c.92C>T (MAGI1))

Chromosome 3
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.66023892G>A
DNA change (hg38) -
Published as MAGI1(NM_001033057.1):c.92C>T (p.(Thr31Met)), MAGI1(NM_015520.1):c.92C>T (p.T31M)
ISCN -
DB-ID MAGI1_000007 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) 0.00038 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 13:16:32 +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     
MAGI1 NM_004742.2 -?/. - c.92C>T r.(?) p.(Thr31Met)


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