RGD:14736853 Rat Genome Database

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Variant: RGD:14736853 -  Homo sapiens

RGD ID: 14736853
RS ID: rs112797038
ClinVar ID: CV668320
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LPIN2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 18 2,927,502
GRCh38 18 2,927,504
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_014646.2:c.1710+218G>A
NG_007507.1:g.89444G>A
NC_000018.10:g.2927504C>T
NC_000018.9:g.2927502C>T
More... 		06/14/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LPIN2
Accession:NM_001375809
Location:INTRON

Gene Symbol:LPIN2
Accession:XM_017026099
Location:INTRON

Gene Symbol:LPIN2
Accession:XM_047437958
Location:INTRON

Gene Symbol:LPIN2
Accession:XM_005258177
Location:INTRON

Gene Symbol:LPIN2
Accession:XM_047437959
Location:INTRON

Gene Symbol:LPIN2
Accession:NM_014646
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 RCV000838674 CLINVAR
dbSNP (RS) rs112797038 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LPIN2 CLINVAR
OMIM 605519 CLINVAR