RGD:155710698 Rat Genome Database

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Variant: RGD:155710698 -  Homo sapiens

RGD ID: 155710698
ClinVar ID: CV1805837
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LAMA4  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 6 112,513,052
GRCh38 6 112,191,850
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000006.11:g.112513052T>C
NM_002290.3:c.504A>G
LRG_433t2:c.504A>G
NM_001105206.3:c.504A>G
More... 		02/20/2020 synonymous variant likely benign

Variant Details
Variant Transcripts
Gene Symbol:LAMA4
Accession:XM_005266983
Location:INTRON

Gene Symbol:LAMA4
Accession:NM_001105207
Location:INTRON

Gene Symbol:LAMA4
Accession:NM_001105209
Location:INTRON

Gene Symbol:LAMA4
Accession:XM_017010854
Location:INTRON

Gene Symbol:LAMA4
Accession:NM_002290
Location:INTRON

Gene Symbol:LAMA4
Accession:XM_005266984
Location:INTRON

Gene Symbol:LAMA4
Accession:XM_047418770
Location:INTRON

Gene Symbol:LAMA4
Accession:XM_047418769
Location:INTRON

Gene Symbol:LAMA4
Accession:NM_001105206
Location:INTRON

Gene Symbol:LAMA4
Accession:XM_047418771
Location:INTRON

Gene Symbol:LAMA4
Accession:NM_001105208
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV002335704 CLINVAR
MedGen CN230736 CLINVAR
NCBI Gene LAMA4 CLINVAR
OMIM 600133 CLINVAR