Variant #0000887980 (NC_000007.13:g.77824247C>T, NM_012301.3:c.2213G>A (MAGI2))

Chromosome 7
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.77824247C>T
DNA change (hg38) -
Published as MAGI2(NM_012301.3):c.2213G>A (p.(Arg738Gln)), MAGI2(NM_012301.4):c.2213G>A (p.R738Q)
ISCN -
DB-ID MAGI2_000032 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) 0.00199 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAGI2 NM_012301.3 -?/. - c.2213G>A r.(?) p.(Arg738Gln)


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