RGD:407532400 Rat Genome Database

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Variant: RGD:407532400 -  Homo sapiens

RGD ID: 407532400
ClinVar ID: CV3493074
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TUT1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 62,344,390
GRCh38 11 62,576,918
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001367906.1:c.1311C>T
NM_022830.3:c.1370C>T
NC_000011.10:g.62576918G>A
NC_000011.9:g.62344390G>A
More... 		03/29/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004683044 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene TUT1 CLINVAR
OMIM 610641 CLINVAR