RGD:150447026 Rat Genome Database

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Variant: RGD:150447026 -  Homo sapiens

RGD ID: 150447026
RS ID: rs2671266
ClinVar ID: CV1270243
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EPHX1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 1 226,027,196
GRCh38 1 225,839,495
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001378432.1:c.365-2871C>T
NM_001378431.1:c.494+149C>T
NM_001378428.1:c.695+149C>T
NM_000120.4:c.722+149C>T
More... 		11/11/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:EPHX1
Accession:NM_001136018
Location:INTRON

Gene Symbol:EPHX1
Accession:NM_000120
Location:INTRON

Gene Symbol:EPHX1
Accession:NM_001378430
Location:INTRON

Gene Symbol:EPHX1
Accession:NM_001291163
Location:INTRON

Gene Symbol:EPHX1
Accession:NM_001378427
Location:INTRON

Gene Symbol:EPHX1
Accession:NM_001378431
Location:INTRON

Gene Symbol:EPHX1
Accession:NM_001378426
Location:INTRON

Gene Symbol:EPHX1
Accession:NM_001378429
Location:INTRON

Gene Symbol:EPHX1
Accession:NM_001378432
Location:INTRON

Gene Symbol:EPHX1
Accession:NM_001378428
Location:INTRON

Gene Symbol:EPHX1
Accession:NR_165624
Location:INTRON;NON-CODING

Gene Symbol:EPHX1
Accession:NR_165625
Location:INTRON;NON-CODING

Gene Symbol:EPHX1
Accession:NR_165626
Location:INTRON;NON-CODING

Gene Symbol:EPHX1
Accession:NR_165627
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001691377 CLINVAR
dbSNP (RS) rs2671266 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene EPHX1 CLINVAR
OMIM 132810 CLINVAR