RGD:329955194 Rat Genome Database

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Variant: RGD:329955194 -  Homo sapiens

RGD ID: 329955194
ClinVar ID: CV2671135
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC107986822  PON2  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 7 95,039,206
GRCh38 7 95,409,894
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001018161.2:c.659+7C>T
NM_000305.3:c.695+7C>T
NG_008725.1:g.30179C>T
NC_000007.14:g.95409894G>A
More... 		05/18/2023 intron variant uncertain significance AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:PON2
Accession:XM_005250453
Location:INTRON

Gene Symbol:PON2
Accession:NM_000305
Location:INTRON

Gene Symbol:PON2
Accession:NM_001018161
Location:INTRON

Gene Symbol:PON2
Accession:XM_017012357
Location:INTRON

Gene Symbol:LOC107986822
Accession:XR_007060439
Location:INTRON;NON-CODING

Gene Symbol:LOC107986822
Accession:XR_001745283
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003236408 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene PON2 CLINVAR
OMIM 602447 CLINVAR