RGD:150437451 Rat Genome Database

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Variant: RGD:150437451 -  Homo sapiens

RGD ID: 150437451
RS ID: rs12112612
ClinVar ID: CV1237870
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LAMB1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 107,575,558
GRCh38 7 107,935,113
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002291.3:c.4188+302C>T
NG_023255.1:g.73247C>T
NC_000007.14:g.107935113G>A
NC_000007.13:g.107575558G>A
 06/26/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:LAMB1
Accession:XM_047420359
Location:INTRON

Gene Symbol:LAMB1
Accession:XM_047420360
Location:INTRON

Gene Symbol:LAMB1
Accession:NM_002291
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001644368 CLINVAR
dbSNP (RS) rs12112612 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LAMB1 CLINVAR
OMIM 150240 CLINVAR