RGD:156348191 Rat Genome Database

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Variant: RGD:156348191 -  Homo sapiens

RGD ID: 156348191
ClinVar ID: CV2128933
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FANCE  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 6 35,426,062
GRCh38 6 35,458,285
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_007104.1:c.-10150C>T
NM_021922.3:c.970-12C>T
LRG_498:g.10925C>T
NG_011708.1:g.10925C>T
More... 		03/25/2022 intron variant likely benign
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:FANCE
Accession:NM_021922
Location:INTRON

Gene Symbol:FANCE
Accession:XM_005248887
Location:INTRON

Gene Symbol:FANCE
Accession:XM_005248885
Location:INTRON

Gene Symbol:FANCE
Accession:XM_005248886
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:FANCE
Accession:XM_011514343
Location:INTRON

Gene Symbol:FANCE
Accession:XM_047418300
Location:INTRON

Gene Symbol:FANCE
Accession:XM_047418303
Location:INTRON

Gene Symbol:FANCE
Accession:XM_047418301
Location:INTRON

Gene Symbol:FANCE
Accession:XM_047418302
Location:INTRON

Gene Symbol:FANCE
Accession:NM_001410876
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002966095 CLINVAR
MedGen C3160739 CLINVAR
NCBI Gene FANCE CLINVAR
OMIM 600901 CLINVAR
  613976 CLINVAR