RGD:8649388 Rat Genome Database

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Variant: RGD:8649388 -  Homo sapiens

RGD ID: 8649388
ClinVar ID: CV125962
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CALN1  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 71,374,444
GRCh38 7 71,909,459
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000007.14:g.71909459T>A
NC_000007.13:g.71374444T>A
NM_001017440.2:c.376-98967A>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:CALN1
Accession:XM_011516596
Location:INTRON

Gene Symbol:CALN1
Accession:XM_017012679
Location:INTRON

Gene Symbol:CALN1
Accession:XM_017012678
Location:INTRON

Gene Symbol:CALN1
Accession:NM_031468
Location:INTRON

Gene Symbol:CALN1
Accession:NM_001017440
Location:INTRON

Gene Symbol:CALN1
Accession:XM_017012682
Location:INTRON

Gene Symbol:CALN1
Accession:XM_017012680
Location:INTRON

Gene Symbol:CALN1
Accession:XM_017012677
Location:INTRON

Gene Symbol:CALN1
Accession:XM_017012676
Location:INTRON

Gene Symbol:CALN1
Accession:XM_047420910
Location:INTRON

Gene Symbol:CALN1
Accession:XM_011516594
Location:INTRON

Gene Symbol:CALN1
Accession:XM_011516597
Location:INTRON

Gene Symbol:CALN1
Accession:NM_001363460
Location:INTRON

Gene Symbol:CALN1
Accession:XM_047420911
Location:INTRON

Gene Symbol:CALN1
Accession:XM_017012683
Location:INTRON

Variant Samples