RGD:150423994 Rat Genome Database

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Variant: RGD:150423994 -  Homo sapiens

RGD ID: 150423994
RS ID: rs116485090
ClinVar ID: CV1185352
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LPIN2  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 18 2,923,925
GRCh38 18 2,923,927
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_174t1:c.2088-66C>G
NM_001375808.2:c.2088-66C>G
NM_001375809.1:c.2088-66C>G
NM_014646.2:c.2088-66C>G
More... 		10/05/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LPIN2
Accession:XM_047437958
Location:INTRON

Gene Symbol:LPIN2
Accession:XM_047437959
Location:INTRON

Gene Symbol:LPIN2
Accession:NM_014646
Location:INTRON

Gene Symbol:LPIN2
Accession:XM_017026099
Location:INTRON

Gene Symbol:LPIN2
Accession:NM_001375809
Location:INTRON

Gene Symbol:LPIN2
Accession:XM_005258177
Location:INTRON

Gene Symbol:LPIN2
Accession:NM_001375808
Location:INTRON

Gene Symbol:LPIN2
Accession:XR_935074
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001556065 CLINVAR
dbSNP (RS) rs116485090 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LPIN2 CLINVAR
OMIM 605519 CLINVAR