RGD:28881205 Rat Genome Database

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Variant: RGD:28881205 -  Homo sapiens

RGD ID: 28881205
RS ID: rs371579247
ClinVar ID: CV863391
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LAMB3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 209,788,354
GRCh38 1 209,615,009
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001017402.2:c.*262G>A
NG_007116.1:g.42467G>A
NC_000001.11:g.209615009C>T
NM_001127641.1:c.*262G>A
More... 		01/12/2018 3 prime utr variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:LAMB3
Accession:XM_017001272
Location:3UTRS;EXON

Gene Symbol:LAMB3
Accession:NM_000228
Location:3UTRS;EXON

Gene Symbol:LAMB3
Accession:NM_001017402
Location:3UTRS;EXON

Gene Symbol:LAMB3
Accession:NM_001127641
Location:3UTRS;EXON

Gene Symbol:LAMB3
Accession:XM_005273124
Location:3UTRS;EXON

Gene Symbol:LAMB3
Accession:XM_047420351
Location:3UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001096782 CLINVAR
dbSNP (RS) rs371579247 CLINVAR
MedGen C0079301 CLINVAR
NCBI Gene LAMB3 CLINVAR
OMIM 150310 CLINVAR