RGD:150499751 Rat Genome Database

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Variant: RGD:150499751 -  Homo sapiens

RGD ID: 150499751
RS ID: rs6931532
ClinVar ID: CV1224648
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GTF2H5  
Reference Nucleotide: A
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 6 158,591,619
GRCh38 6 158,170,587
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_207118.3:c.35+49T>G
LRG_469:g.7241T>G
NG_032889.1:g.2694A>C
NG_011758.1:g.7241T>G
More... 		07/05/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:GTF2H5
Accession:NM_207118
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001620479 CLINVAR
dbSNP (RS) rs6931532 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GTF2H5 CLINVAR
OMIM 608780 CLINVAR