RGD:407487194 Rat Genome Database

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Variant: RGD:407487194 -  Homo sapiens

RGD ID: 407487194
ClinVar ID: CV3420888
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: BACH2  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 6 90,660,313
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000006.11:g.90660313G>C
NM_021813.2:c.1512C>G
NP_001164265.1:p.Ile504Met
NP_068585.1:p.Ile504Met
More... 		06/13/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004603718 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene BACH2 CLINVAR
OMIM 605394 CLINVAR