RGD:15139318 Rat Genome Database

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Variant: RGD:15139318 -  Homo sapiens

RGD ID: 15139318
RS ID: rs61755651
ClinVar ID: CV779763
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RGS6  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 14 72,431,599
GRCh38 14 71,964,882
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000014.9:g.71964882C>T
NC_000014.8:g.72431599C>T
NM_004296.6:c.84+7C>T
NM_001204423.2:c.-22+32649C>T
More... 		08/15/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:RGS6
Accession:NM_001204423
Location:5UTRS;INTRON

Gene Symbol:RGS6
Accession:NM_001204424
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001204417
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370281
Location:INTRON

Gene Symbol:RGS6
Accession:XM_047431990
Location:INTRON

Gene Symbol:RGS6
Accession:XM_017021822
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370287
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370276
Location:INTRON

Gene Symbol:RGS6
Accession:XM_024449759
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001204418
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370291
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370278
Location:INTRON

Gene Symbol:RGS6
Accession:XM_017021820
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370271
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370284
Location:INTRON

Gene Symbol:RGS6
Accession:NM_004296
Location:INTRON

Gene Symbol:RGS6
Accession:XM_017021825
Location:INTRON

Gene Symbol:RGS6
Accession:XM_024449760
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370274
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370293
Location:INTRON

Gene Symbol:RGS6
Accession:XM_011537397
Location:INTRON

Gene Symbol:RGS6
Accession:XM_024449763
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370294
Location:INTRON

Gene Symbol:RGS6
Accession:XM_047431988
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370270
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370280
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370288
Location:INTRON

Gene Symbol:RGS6
Accession:XM_017021830
Location:INTRON

Gene Symbol:RGS6
Accession:XM_017021828
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370290
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001204422
Location:INTRON

Gene Symbol:RGS6
Accession:XM_017021831
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370289
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370282
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370272
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001204419
Location:INTRON

Gene Symbol:RGS6
Accession:XM_024449764
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370292
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001204416
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001204420
Location:INTRON

Gene Symbol:RGS6
Accession:XM_024449776
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370273
Location:INTRON

Gene Symbol:RGS6
Accession:XM_017021827
Location:INTRON

Gene Symbol:RGS6
Accession:XM_017021832
Location:INTRON

Gene Symbol:RGS6
Accession:XM_024449761
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370275
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370283
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370277
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001204421
Location:INTRON

Gene Symbol:RGS6
Accession:XM_017021826
Location:INTRON

Gene Symbol:RGS6
Accession:XM_017021833
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370286
Location:INTRON

Gene Symbol:RGS6
Accession:NM_001370279
Location:INTRON

Gene Symbol:RGS6
Accession:XM_047431987
Location:INTRON

Gene Symbol:RGS6
Accession:XM_047431985
Location:INTRON

Gene Symbol:RGS6
Accession:NR_135235
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000965944 CLINVAR
dbSNP (RS) rs61755651 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene RGS6 CLINVAR
OMIM 603894 CLINVAR