RGD:407484722 Rat Genome Database

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Variant: RGD:407484722 -  Homo sapiens

RGD ID: 407484722
ClinVar ID: CV3449677
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC129998720  MAGI2  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 77,648,892
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.4066C>G
NM_012301.4:c.4108C>G
NG_011487.2:g.1439000C>G
NG_178166.1:g.152G>C
More... 		03/15/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004640577 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene LOC129998720 CLINVAR
  MAGI2 CLINVAR
OMIM 606382 CLINVAR