RGD:8630536 Rat Genome Database

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Variant: RGD:8630536 -  Homo sapiens

RGD ID: 8630536
ClinVar ID: CV85691
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: PHLDB2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 111,630,481
GRCh38 3 111,911,634
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001134438.1:c.1336-1685G>A
NM_001134439.1:c.1336-1685G>A
NM_145753.2:c.1336-1685G>A
NM_001134437.1:c.1417-1685G>A
More... 		intron|intron variant not provided Malignant melanoma, somatic

Variant Details
Variant Transcripts
Gene Symbol:PHLDB2
Accession:NM_001134437
Location:INTRON

Gene Symbol:PHLDB2
Accession:NM_001134438
Location:INTRON

Gene Symbol:PHLDB2
Accession:NM_145753
Location:INTRON

Gene Symbol:PHLDB2
Accession:NM_001134439
Location:INTRON

Variant Samples