RGD:156177165 Rat Genome Database

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Variant: RGD:156177165 -  Homo sapiens

RGD ID: 156177165
ClinVar ID: CV2010421
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC126806147  LPIN1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 11,919,639
GRCh38 2 11,779,513
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001349199.2:c.723-6C>T
NM_001349200.2:c.723-6C>T
NM_001349201.2:c.723-6C>T
NM_145693.4:c.723-6C>T
More... 		06/23/2022 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LPIN1
Accession:NM_145693
Location:INTRON

Gene Symbol:LPIN1
Accession:NM_001261428
Location:INTRON

Gene Symbol:LPIN1
Accession:NM_001261427
Location:INTRON

Gene Symbol:LPIN1
Accession:NM_001349208
Location:INTRON

Gene Symbol:LPIN1
Accession:NM_001349207
Location:INTRON

Gene Symbol:LPIN1
Accession:NM_001349204
Location:INTRON

Gene Symbol:LPIN1
Accession:NM_001349202
Location:INTRON

Gene Symbol:LPIN1
Accession:NM_001349200
Location:INTRON

Gene Symbol:LPIN1
Accession:NM_001349199
Location:INTRON

Gene Symbol:LPIN1
Accession:NM_001349206
Location:INTRON

Gene Symbol:LPIN1
Accession:NM_001349203
Location:INTRON

Gene Symbol:LPIN1
Accession:NM_001349201
Location:INTRON

Gene Symbol:LPIN1
Accession:NM_001349205
Location:INTRON

Gene Symbol:LPIN1
Accession:NR_146080
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002710666 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LOC126806147 CLINVAR
  LPIN1 CLINVAR
OMIM 605518 CLINVAR