RGD:28902962 Rat Genome Database

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Variant: RGD:28902962 -  Homo sapiens

RGD ID: 28902962
RS ID: rs867272212
ClinVar ID: CV892518
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC124900602  SNCA  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 90,646,487
GRCh38 4 89,725,336
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.117961C>T
NC_000004.12:g.89725336G>A
NC_000004.11:g.90646487G>A
NR_164676.1:n.2013C>T
More...
01/12/2018 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:SNCA
Accession:NM_001146055
Location:3UTRS;EXON

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

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

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

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

Gene Symbol:SNCA
Accession:NM_001375286
Location:3UTRS;EXON

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

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

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

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

Gene Symbol:LOC124900602
Accession:XR_007058466
Location:EXON;NON-CODING

Gene Symbol:SNCA
Accession:XM_011532205
Location:INTRON

Gene Symbol:SNCA
Accession:XM_011532203
Location:INTRON

Gene Symbol:SNCA
Accession:XM_011532206
Location:INTRON

Gene Symbol:SNCA
Accession:XM_011532204
Location:INTRON

Gene Symbol:SNCA
Accession:XM_011532207
Location:INTRON

Gene Symbol:SNCA
Accession:XM_047416097
Location:INTRON

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

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

Gene Symbol:LOC124900602
Accession:XR_007058465
Location:INTRON;NON-CODING

Gene Symbol:LOC105377329
Accession:XR_001741764
Location:INTRON;NON-CODING

Gene Symbol:LOC105377329
Accession:XR_938983
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001157354 CLINVAR
dbSNP (RS) rs867272212 CLINVAR
MedGen CN239359 CLINVAR
NCBI Gene SNCA CLINVAR
OMIM 163890 CLINVAR