RGD:15104259 Rat Genome Database

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Variant: RGD:15104259 -  Homo sapiens

RGD ID: 15104259
RS ID: rs761799071
ClinVar ID: CV782731
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LAMB1  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 7 107,635,404
GRCh38 7 107,994,959
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.351T>C
NG_023255.1:g.13401T>C
NC_000007.14:g.107994959A>G
NC_000007.13:g.107635404A>G
More... 		10/17/2018 synonymous variant likely benign none provided

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

Gene Symbol:LAMB1
Accession:NM_002291
Location:EXON

Gene Symbol:LAMB1
Accession:XM_047420360
Location:EXON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000976183 CLINVAR
dbSNP (RS) rs761799071 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene LAMB1 CLINVAR
OMIM 150240 CLINVAR