RGD:407532425 Rat Genome Database

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Variant: RGD:407532425 -  Homo sapiens

RGD ID: 407532425
ClinVar ID: CV3493099
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TUT7  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 9 88,967,949
GRCh38 9 86,353,034
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001330718.2:c.-2131A>T
NM_001185059.2:c.166A>T
NM_001185074.2:c.166A>T
NM_024617.4:c.166A>T
More... 		05/02/2024 5 prime utr variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004683069 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene TUT7 CLINVAR
OMIM 613467 CLINVAR