RGD:150539299 Rat Genome Database

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Variant: RGD:150539299 -  Homo sapiens

RGD ID: 150539299
RS ID: rs185158687
ClinVar ID: CV1308629
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ELMOD3  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 2 85,590,199
GRCh38 2 85,363,076
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001135022.2:c.130-21A>G
NM_001329793.2:c.130-21A>G
NG_051291.1:g.13683A>G
NC_000002.12:g.85363076A>G
More... 		07/29/2020 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ELMOD3
Accession:XM_047445965
Location:INTRON

Gene Symbol:ELMOD3
Accession:XM_047445974
Location:INTRON

Gene Symbol:ELMOD3
Accession:NM_001329792
Location:INTRON

Gene Symbol:ELMOD3
Accession:XM_047445966
Location:INTRON

Gene Symbol:ELMOD3
Accession:XM_047445978
Location:INTRON

Gene Symbol:ELMOD3
Accession:NM_001135022
Location:INTRON

Gene Symbol:ELMOD3
Accession:XM_024453171
Location:INTRON

Gene Symbol:ELMOD3
Accession:NM_001329793
Location:INTRON

Gene Symbol:ELMOD3
Accession:XM_047445971
Location:INTRON

Gene Symbol:ELMOD3
Accession:XM_047445968
Location:INTRON

Gene Symbol:ELMOD3
Accession:XM_047445963
Location:INTRON

Gene Symbol:ELMOD3
Accession:XM_047445977
Location:INTRON

Gene Symbol:ELMOD3
Accession:NM_001135023
Location:INTRON

Gene Symbol:ELMOD3
Accession:NM_001329791
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:ELMOD3
Accession:XM_047445973
Location:INTRON

Gene Symbol:ELMOD3
Accession:XM_047445979
Location:INTRON

Gene Symbol:ELMOD3
Accession:XM_047445969
Location:INTRON

Gene Symbol:ELMOD3
Accession:NM_001135021
Location:INTRON

Gene Symbol:ELMOD3
Accession:XM_047445972
Location:INTRON

Gene Symbol:ELMOD3
Accession:XM_047445964
Location:INTRON

Gene Symbol:ELMOD3
Accession:NM_032213
Location:INTRON

Gene Symbol:ELMOD3
Accession:XM_047445975
Location:INTRON

Gene Symbol:ELMOD3
Accession:XM_024453169
Location:INTRON

Gene Symbol:ELMOD3
Accession:XM_047445976
Location:INTRON

Gene Symbol:ELMOD3
Accession:XM_047445967
Location:INTRON

Gene Symbol:ELMOD3
Accession:XM_024453170
Location:INTRON

Gene Symbol:ELMOD3
Accession:NR_138133
Location:INTRON;NON-CODING

Gene Symbol:ELMOD3
Accession:NR_138131
Location:INTRON;NON-CODING

Gene Symbol:ELMOD3
Accession:NR_138132
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001766133 CLINVAR
dbSNP (RS) rs185158687 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ELMOD3 CLINVAR
OMIM 615427 CLINVAR