RGD:14745300 Rat Genome Database

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Variant: RGD:14745300 -  Homo sapiens

RGD ID: 14745300
RS ID: rs2245677
ClinVar ID: CV663820
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127816054  LRSAM1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 130,251,512
GRCh38 9 127,489,233
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001005374.4:c.1348-211G>A
NM_001384142.1:c.1348-211G>A
NM_001190723.3:c.1348-211G>A
NM_138361.5:c.1348-211G>A
More...
06/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LRSAM1
Accession:NM_001005373
Location:INTRON

Gene Symbol:LRSAM1
Accession:NM_001190723
Location:INTRON

Gene Symbol:LRSAM1
Accession:NM_138361
Location:INTRON

Gene Symbol:LRSAM1
Accession:NM_001005374
Location:INTRON

Gene Symbol:LRSAM1
Accession:NM_001384142
Location:INTRON

Gene Symbol:LRSAM1
Accession:NM_001384143
Location:INTRON

Gene Symbol:LRSAM1
Accession:NM_001384144
Location:INTRON

Gene Symbol:LRSAM1
Accession:XM_047424058
Location:INTRON

Gene Symbol:LRSAM1
Accession:XM_047424059
Location:INTRON

Gene Symbol:LRSAM1
Accession:NR_168892
Location:INTRON;NON-CODING

Gene Symbol:LRSAM1
Accession:NR_168891
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000843278 CLINVAR
dbSNP (RS) rs2245677 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LRSAM1 CLINVAR
OMIM 610933 CLINVAR