RGD:15143501 Rat Genome Database

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Variant: RGD:15143501 -  Homo sapiens

RGD ID: 15143501
RS ID: rs192180976
ClinVar ID: CV744230
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SUGCT  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 40,535,879
GRCh38 7 40,496,280
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001193313.2:c.987-4T>C
NM_001193312.2:c.843-4T>C
NM_024728.3:c.876-4T>C
NC_000007.13:g.40535879T>C
More... 		10/17/2017 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SUGCT
Accession:NM_001193311
Location:INTRON

Gene Symbol:SUGCT
Accession:NM_001193312
Location:INTRON

Gene Symbol:SUGCT
Accession:XM_011515529
Location:INTRON

Gene Symbol:SUGCT
Accession:XM_011515530
Location:INTRON

Gene Symbol:SUGCT
Accession:XM_011515526
Location:INTRON

Gene Symbol:SUGCT
Accession:XM_006715775
Location:INTRON

Gene Symbol:SUGCT
Accession:XM_017012622
Location:INTRON

Gene Symbol:SUGCT
Accession:XM_047420843
Location:INTRON

Gene Symbol:SUGCT
Accession:XM_047420840
Location:INTRON

Gene Symbol:SUGCT
Accession:NM_001193313
Location:INTRON

Gene Symbol:SUGCT
Accession:XM_047420842
Location:INTRON

Gene Symbol:SUGCT
Accession:NM_024728
Location:INTRON

Gene Symbol:SUGCT
Accession:XM_011515525
Location:INTRON

Gene Symbol:SUGCT
Accession:XM_047420841
Location:INTRON

Gene Symbol:SUGCT
Accession:XM_011515527
Location:INTRON

Gene Symbol:SUGCT
Accession:XM_017012621
Location:INTRON

Gene Symbol:SUGCT
Accession:XR_007060157
Location:INTRON;NON-CODING

Gene Symbol:SUGCT
Accession:XR_007060158
Location:INTRON;NON-CODING

Gene Symbol:SUGCT
Accession:XR_007060156
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000899848 CLINVAR
dbSNP (RS) rs192180976 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SUGCT CLINVAR
OMIM 609187 CLINVAR