RGD:407504349 Rat Genome Database

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Variant: RGD:407504349 -  Homo sapiens

RGD ID: 407504349
ClinVar ID: CV3484960
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ATG7  
Reference Nucleotide: T
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 3 11,340,200
GRCh38 3 11,298,726
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001349238.2:c.-781T>A
NM_001136031.3:c.31T>A
NM_001144912.2:c.31T>A
NM_001349232.2:c.31T>A
More... 		05/29/2024 5 prime utr variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004670501 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene ATG7 CLINVAR
OMIM 608760 CLINVAR