RGD:8633930 Rat Genome Database

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Variant: RGD:8633930 -  Homo sapiens

RGD ID: 8633930
ClinVar ID: CV89146
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KCNJ5  KCNJ5-AS1  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 128,774,456
GRCh38 11 128,904,561
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_333t1:c.-10-6703C>A
NM_000890.3:c.-10-6703C>A
LRG_333:g.18144C>A
NG_023406.2:g.18144C>A
More... 		intron|intron variant|missense variant|non-coding transcript variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:KCNJ5
Accession:NM_000890
Location:5UTRS;INTRON

Gene Symbol:KCNJ5
Accession:NM_001354169
Location:5UTRS;INTRON

Gene Symbol:KCNJ5-AS1
Accession:NR_169216
Location:EXON;NON-CODING

Gene Symbol:KCNJ5-AS1
Accession:NR_169217
Location:EXON;NON-CODING

Gene Symbol:KCNJ5-AS1
Accession:NR_169215
Location:EXON;NON-CODING

Gene Symbol:KCNJ5-AS1
Accession:NR_045767
Location:EXON;NON-CODING

Gene Symbol:KCNJ5
Accession:XM_011542810
Location:INTRON

Variant Samples