RGD:407515171 Rat Genome Database

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Variant: RGD:407515171 -  Homo sapiens

RGD ID: 407515171
ClinVar ID: CV3440842
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IGSF10  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 3 151,163,631
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001385060.1:c.4138A>G
NM_001385061.1:c.4138A>G
NM_001385062.1:c.4138A>G
NM_001385063.1:c.4138A>G
More... 		04/09/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004627821 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene IGSF10 CLINVAR
OMIM 617351 CLINVAR