RGD:8625396 Rat Genome Database

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Variant: RGD:8625396 -  Homo sapiens

RGD ID: 8625396
ClinVar ID: CV80519
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ANTXR1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 2 69,330,071
GRCh38 2 69,102,939
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000002.10:g.69183575C>T
NM_053034.2:c.801C>T
NM_018153.3:c.801C>T
NM_032208.2:c.801C>T
More...
synonymous variant|2kb upstream variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:ANTXR1
Accession:NM_032208
Location:EXON

Gene Symbol:ANTXR1
Accession:NM_053034
Location:EXON

Gene Symbol:ANTXR1
Accession:NM_018153
Location:EXON

Gene Symbol:ANTXR1
Accession:XM_017005077
Location:EXON

Gene Symbol:
Accession:
Location:EXON

Gene Symbol:ANTXR1
Accession:XM_017005076
Location:EXON

Gene Symbol:ANTXR1
Accession:NM_001410840
Location:EXON

Variant Samples