RGD:150331772 Rat Genome Database

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Variant: RGD:150331772 -  Homo sapiens

RGD ID: 150331772
RS ID: rs78177862
ClinVar ID: CV1171063
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MME  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 154,878,093
GRCh38 3 155,160,304
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000902.5:c.1602-86G>A
NM_007289.4:c.1602-86G>A
NC_000003.12:g.155160304G>A
NC_000003.11:g.154878093G>A
More... 		01/28/2019 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MME
Accession:XM_006713647
Location:INTRON

Gene Symbol:MME
Accession:XM_047448157
Location:INTRON

Gene Symbol:MME
Accession:NM_007289
Location:INTRON

Gene Symbol:MME
Accession:NM_001354642
Location:INTRON

Gene Symbol:MME
Accession:XM_011512856
Location:INTRON

Gene Symbol:MME
Accession:NM_001354643
Location:INTRON

Gene Symbol:MME
Accession:NM_007288
Location:INTRON

Gene Symbol:MME
Accession:NM_000902
Location:INTRON

Gene Symbol:MME
Accession:NM_007287
Location:INTRON

Gene Symbol:MME
Accession:NM_001354644
Location:INTRON

Gene Symbol:MME
Accession:XM_011512857
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001538768 CLINVAR
dbSNP (RS) rs78177862 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MME CLINVAR
OMIM 120520 CLINVAR