RGD:14729845 Rat Genome Database

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Variant: RGD:14729845 -  Homo sapiens

RGD ID: 14729845
ClinVar ID: CV671622
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FANCI  POLG  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 15 89,860,157
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
NM_002693.2:c.3644-99C>T
NC_000015.10:g.89316926G>A
NC_000015.9:g.89860157G>A
 06/16/2018 likely benign

Variant Details
Variant Transcripts
Gene Symbol:FANCI
Accession:NM_018193
Location:3UTRS;EXON

Gene Symbol:FANCI
Accession:NM_001113378
Location:3UTRS;EXON

Gene Symbol:POLG
Accession:NM_001126131
Location:INTRON

Gene Symbol:POLG
Accession:NM_002693
Location:INTRON

Variant Samples