RGD:8649074 Rat Genome Database

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Variant: RGD:8649074 -  Homo sapiens

RGD ID: 8649074
RS ID: rs121913181
ClinVar ID: CV116899
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IFNGR1  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 6 137,522,488
GRCh38 6 137,201,351
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000416.3:c.734-343C>A
LRG_66t1:c.734-343C>A
LRG_66:g.23080C>A
NG_007394.1:g.23080C>A
More... 		intron|intron variant not provided none provided

Variant Details
Variant Transcripts
Gene Symbol:IFNGR1
Accession:NM_000416
Location:INTRON

Gene Symbol:IFNGR1
Accession:XM_011535793
Location:INTRON

Gene Symbol:IFNGR1
Accession:XM_011535794
Location:INTRON

Gene Symbol:IFNGR1
Accession:XM_006715470
Location:INTRON

Gene Symbol:IFNGR1
Accession:XM_047418726
Location:INTRON

Gene Symbol:IFNGR1
Accession:NM_001363526
Location:INTRON

Gene Symbol:IFNGR1
Accession:NM_001363527
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000097419 CLINVAR
dbSNP (RS) rs121913181 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene IFNGR1 CLINVAR
OMIM 107470 CLINVAR