RGD:152139164 Rat Genome Database

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Variant: RGD:152139164 -  Homo sapiens

RGD ID: 152139164
RS ID: rs114777882
ClinVar ID: CV1549649
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: EXOC3L2  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 19 45,731,531
GRCh38 19 45,228,273
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001382422.1:c.1270-7A>G
NG_054912.2:g.22135A>G
NC_000019.10:g.45228273T>C
NC_000019.9:g.45731531T>C
More... 		07/11/2021 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:EXOC3L2
Accession:NM_001382422
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002156537 CLINVAR
dbSNP (RS) rs114777882 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene EXOC3L2 CLINVAR
OMIM 616927 CLINVAR