RGD:407459901 Rat Genome Database

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Variant: RGD:407459901 -  Homo sapiens

RGD ID: 407459901
ClinVar ID: CV3472610
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: RFTN1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 16,535,262
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000003.11:g.16535262G>A
NM_015150.1:c.115C>T
NP_055965.1:p.Arg39Cys
NM_015150.2:c.115C>T
More... 		04/09/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004658314 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene RFTN1 CLINVAR
OMIM 618210 CLINVAR