RGD:11659775 Rat Genome Database

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Variant: RGD:11659775 -  Homo sapiens

RGD ID: 11659775
RS ID: rs886061036
ClinVar ID: CV305739
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LAMA2  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 6 129,204,288
GRCh38 6 128,883,143
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_409t1:c.-103C>T
LRG_409:g.5003C>T
NG_008678.1:g.5003C>T
NC_000006.12:g.128883143C>T
More... 		01/13/2018 5 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:LAMA2
Accession:NM_001079823
Location:5UTRS;EXON

Gene Symbol:LAMA2
Accession:NM_000426
Location:5UTRS;EXON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000361300 CLINVAR
dbSNP (RS) rs886061036 CLINVAR
MedGen C1842898 CLINVAR
NCBI Gene LAMA2 CLINVAR
OMIM 156225 CLINVAR