RGD:150442828 Rat Genome Database

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Variant: RGD:150442828 -  Homo sapiens

RGD ID: 150442828
RS ID: rs56208271
ClinVar ID: CV1266295
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MME  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 154,801,832
GRCh38 3 155,084,043
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001354642.2:c.-10-115G>A
NM_001354643.1:c.-10-115G>A
NM_001354644.1:c.-10-115G>A
NM_007287.4:c.-10-115G>A
More... 		07/15/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MME
Accession:XM_006713647
Location:5UTRS;INTRON

Gene Symbol:MME
Accession:NM_007288
Location:5UTRS;INTRON

Gene Symbol:MME
Accession:NM_007289
Location:5UTRS;INTRON

Gene Symbol:MME
Accession:NM_000902
Location:5UTRS;INTRON

Gene Symbol:MME
Accession:NM_001354642
Location:5UTRS;INTRON

Gene Symbol:MME
Accession:XM_011512856
Location:5UTRS;INTRON

Gene Symbol:MME
Accession:XM_011512857
Location:5UTRS;INTRON

Gene Symbol:MME
Accession:NM_001354644
Location:5UTRS;INTRON

Gene Symbol:MME
Accession:NM_007287
Location:5UTRS;INTRON

Gene Symbol:MME
Accession:XM_047448157
Location:5UTRS;INTRON

Gene Symbol:MME
Accession:NM_001354643
Location:5UTRS;INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001690731 CLINVAR
dbSNP (RS) rs56208271 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MME CLINVAR
OMIM 120520 CLINVAR