RGD:407498317 Rat Genome Database

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Variant: RGD:407498317 -  Homo sapiens

RGD ID: 407498317
ClinVar ID: CV3479024
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: THSD7A  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 7 11,676,543
GRCh38 7 11,636,916
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_015204.3:c.236T>A
NG_027670.1:g.200282T>A
NG_027670.2:g.200282T>A
NC_000007.14:g.11636916A>T
More... 		05/13/2024 missense variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004668629 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene THSD7A CLINVAR
OMIM 612249 CLINVAR