RGD:150504835 Rat Genome Database

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Variant: RGD:150504835 -  Homo sapiens

RGD ID: 150504835
RS ID: rs2014227
ClinVar ID: CV1211472
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ISCU  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 12 108,962,927
GRCh38 12 108,569,151
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001320042.1:c.*1447G>A
NM_014301.4:c.*235G>A
NM_213595.4:c.*235G>A
NM_001301140.1:c.*360G>A
More...
06/28/2018 3 prime utr variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ISCU
Accession:NM_014301
Location:3UTRS;EXON

Gene Symbol:ISCU
Accession:NM_213595
Location:3UTRS;EXON

Gene Symbol:ISCU
Accession:NM_001301140
Location:3UTRS;EXON

Gene Symbol:ISCU
Accession:NM_001301141
Location:3UTRS;EXON

Gene Symbol:ISCU
Accession:NM_001320042
Location:3UTRS;EXON

Gene Symbol:ISCU
Accession:XM_047428627
Location:3UTRS;EXON

Gene Symbol:ISCU
Accession:NR_135127
Location:EXON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001595637 CLINVAR
dbSNP (RS) rs2014227 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ISCU CLINVAR
OMIM 611911 CLINVAR