RGD:13706316 Rat Genome Database

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Variant: RGD:13706316 -  Homo sapiens

RGD ID: 13706316
RS ID: rs1553680151
ClinVar ID: CV537429
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IMPG2  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 100,949,989
GRCh38 3 101,231,145
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_028284.1:g.94431G>T
NP_057331.2:p.Arg1078Ser
NC_000003.12:g.101231145C>A
NM_016247.4:c.3234G>T
More... 		03/31/2018 missense variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:IMPG2
Accession:NM_016247
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000658967 CLINVAR
dbSNP (RS) rs1553680151 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene IMPG2 CLINVAR
OMIM 607056 CLINVAR