RGD:11648041 Rat Genome Database

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Variant: RGD:11648041 -  Homo sapiens

RGD ID: 11648041
RS ID: rs886059727
ClinVar ID: CV296195
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SNCA  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 90,647,502
GRCh38 4 89,726,351
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_011851.1:g.116946G>T
NC_000004.12:g.89726351C>A
NC_000004.11:g.90647502C>A
NM_000345.4:c.*277G>T
More... 		06/14/2016 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:SNCA
Accession:NM_001375286
Location:3UTRS;EXON

Gene Symbol:SNCA
Accession:NM_001375285
Location:3UTRS;EXON

Gene Symbol:SNCA
Accession:NM_001375290
Location:3UTRS;EXON

Gene Symbol:SNCA
Accession:NM_001146055
Location:3UTRS;EXON

Gene Symbol:SNCA
Accession:NM_000345
Location:3UTRS;EXON

Gene Symbol:SNCA
Accession:NM_001146054
Location:3UTRS;EXON

Gene Symbol:SNCA
Accession:NM_001375287
Location:3UTRS;EXON

Gene Symbol:SNCA
Accession:NM_007308
Location:3UTRS;EXON

Gene Symbol:SNCA
Accession:NM_001375288
Location:3UTRS;EXON

Gene Symbol:SNCA
Accession:NR_164676
Location:EXON;NON-CODING

Gene Symbol:SNCA
Accession:NR_164675
Location:EXON;NON-CODING

Gene Symbol:SNCA
Accession:NR_164674
Location:EXON;NON-CODING

Gene Symbol:SNCA
Accession:XM_011532203
Location:INTRON

Gene Symbol:SNCA
Accession:XM_011532207
Location:INTRON

Gene Symbol:SNCA
Accession:XM_011532206
Location:INTRON

Gene Symbol:SNCA
Accession:XM_011532205
Location:INTRON

Gene Symbol:SNCA
Accession:XM_047416097
Location:INTRON

Gene Symbol:SNCA
Accession:XM_011532204
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000279992 CLINVAR
dbSNP (RS) rs886059727 CLINVAR
MedGen CN239359 CLINVAR
NCBI Gene SNCA CLINVAR
OMIM 163890 CLINVAR