RGD:151774777 Rat Genome Database

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Variant: RGD:151774777 -  Homo sapiens

RGD ID: 151774777
RS ID: rs200961860
ClinVar ID: CV1424181
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MME  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 3 154,856,024
GRCh38 3 155,138,235
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.854A>G
NM_001354642.2:c.854A>G
NM_001354643.1:c.854A>G
NM_007287.4:c.854A>G
More... 		08/12/2021 missense variant uncertain significance none provided

Variant Details
Variant Transcripts
Gene Symbol:MME
Accession:XM_011512856
Location:EXON

Gene Symbol:MME
Accession:XM_011512857
Location:EXON

Gene Symbol:MME
Accession:NM_000902
Location:EXON

Gene Symbol:MME
Accession:NM_001354642
Location:EXON

Gene Symbol:MME
Accession:NM_007289
Location:EXON

Gene Symbol:MME
Accession:NM_001354643
Location:EXON

Gene Symbol:MME
Accession:XM_047448157
Location:EXON

Gene Symbol:MME
Accession:NM_007287
Location:EXON

Gene Symbol:MME
Accession:NM_007288
Location:EXON

Gene Symbol:MME
Accession:XM_006713647
Location:EXON

Gene Symbol:MME
Accession:NM_001354644
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:20692264   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002025700 CLINVAR
dbSNP (RS) rs200961860 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MME CLINVAR
OMIM 120520 CLINVAR