RGD:150516618 Rat Genome Database

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Variant: RGD:150516618 -  Homo sapiens

RGD ID: 150516618
RS ID: rs2528649
ClinVar ID: CV1227152
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LAMB1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 107,591,916
GRCh38 7 107,951,471
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.3295-149G>A
NG_023255.1:g.56889G>A
NC_000007.14:g.107951471C>T
NC_000007.13:g.107591916C>T
 06/30/2018 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 RCV001639250 CLINVAR
dbSNP (RS) rs2528649 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene LAMB1 CLINVAR
OMIM 150240 CLINVAR