RGD:150455067 Rat Genome Database

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Variant: RGD:150455067 -  Homo sapiens

RGD ID: 150455067
RS ID: rs79161028
ClinVar ID: CV1220403
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LPIN1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 2 11,954,942
GRCh38 2 11,814,816
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001349208.2:c.2289-272T>C
NM_001349207.2:c.2340-272T>C
NM_001261428.3:c.2397-272T>C
NM_001349205.2:c.2250-272T>C
More... 		07/09/2018 intron variant 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 Information

Database Acc Id Source(s)
ClinVar RCV001612496 CLINVAR
dbSNP (RS) rs79161028 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LPIN1 CLINVAR
OMIM 605518 CLINVAR