RGD:407517586 Rat Genome Database

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Variant: RGD:407517586 -  Homo sapiens

RGD ID: 407517586
ClinVar ID: CV3485942
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TCP1  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 6 160,202,114
GRCh38 6 159,781,082
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
NM_001008897.2:c.361C>G
NM_030752.3:c.826C>G
NC_000006.12:g.159781082G>C
NC_000006.11:g.160202114G>C
More... 		04/15/2024 missense variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004675663 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene TCP1 CLINVAR
OMIM 186980 CLINVAR