RGD:150421890 Rat Genome Database

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Variant: RGD:150421890 -  Homo sapiens

RGD ID: 150421890
RS ID: rs113646446
ClinVar ID: CV1181342
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MYH11  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 16 15,878,701
GRCh38 16 15,784,844
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1401t1:c.633+1786T>C
LRG_1401t2:c.634-126T>C
NM_002474.3:c.633+1786T>C
NM_022844.3:c.633+1786T>C
More... 		07/15/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MYH11
Accession:NM_002474
Location:INTRON

Gene Symbol:MYH11
Accession:NM_022844
Location:INTRON

Gene Symbol:MYH11
Accession:NM_001040114
Location:INTRON

Gene Symbol:MYH11
Accession:NM_001040113
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001552221 CLINVAR
dbSNP (RS) rs113646446 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MYH11 CLINVAR
OMIM 160745 CLINVAR