RGD:15163880 Rat Genome Database

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Variant: RGD:15163880 -  Homo sapiens

RGD ID: 15163880
RS ID: rs367721228
ClinVar ID: CV760948
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ARHGAP6  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 11,162,373
GRCh38 X 11,144,253
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_013423.3:c.1299-5G>T
NM_001287242.2:c.1368-5G>T
NM_006125.3:c.1908-5G>T
NM_013427.3:c.1908-5G>T
More... 		06/16/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ARHGAP6
Accession:NM_006125
Location:INTRON

Gene Symbol:ARHGAP6
Accession:NM_013427
Location:INTRON

Gene Symbol:ARHGAP6
Accession:NM_001287242
Location:INTRON

Gene Symbol:ARHGAP6
Accession:NM_013423
Location:INTRON

Gene Symbol:ARHGAP6
Accession:NR_109776
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000926240 CLINVAR
dbSNP (RS) rs367721228 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene ARHGAP6 CLINVAR
OMIM 300118 CLINVAR