RGD:405290105 Rat Genome Database

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Variant: RGD:405290105 -  Homo sapiens

RGD ID: 405290105
ClinVar ID: CV3206016
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MAGI2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 77,708,260
GRCh38 7 78,078,943
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001301128.2:c.3664+4C>T
NM_012301.4:c.3706+4C>T
NG_011487.2:g.1379632C>T
NC_000007.14:g.78078943G>A
More... 		09/01/2022 intron variant likely benign MAGI2-related condition

Variant Details
Variant Transcripts
Gene Symbol:MAGI2
Accession:XM_017012841
Location:INTRON

Gene Symbol:MAGI2
Accession:NM_001301128
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_017012842
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_047421092
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_011516720
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_017012846
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_017012840
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_017012845
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_047421093
Location:INTRON

Gene Symbol:MAGI2
Accession:NM_012301
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_017012844
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_011516718
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_017012843
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_011516728
Location:INTRON

Gene Symbol:MAGI2
Accession:XM_017012847
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003962135 CLINVAR
NCBI Gene MAGI2 CLINVAR
OMIM 606382 CLINVAR