RGD:401904236 Rat Genome Database

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Variant: RGD:401904236 -  Homo sapiens

RGD ID: 401904236
ClinVar ID: CV2816529
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: NAV2  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 11 20,124,794
GRCh38 11 20,103,248
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001111018.2:c.6226-7A>G
NM_145117.5:c.6418-7A>G
NM_182964.6:c.6427-7A>G
NM_001244963.2:c.6595-7A>G
More... 		04/01/2023 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:NAV2
Accession:XM_005253214
Location:INTRON

Gene Symbol:NAV2
Accession:NM_145117
Location:INTRON

Gene Symbol:NAV2
Accession:XM_006718366
Location:INTRON

Gene Symbol:NAV2
Accession:XM_011520447
Location:INTRON

Gene Symbol:NAV2
Accession:NM_001244963
Location:INTRON

Gene Symbol:NAV2
Accession:XM_011520446
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427814
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427838
Location:INTRON

Gene Symbol:NAV2
Accession:NM_001111018
Location:INTRON

Gene Symbol:NAV2
Accession:NM_001111019
Location:INTRON

Gene Symbol:NAV2
Accession:XM_017018521
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427825
Location:INTRON

Gene Symbol:NAV2
Accession:XM_006718365
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427828
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427831
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427837
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427820
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427817
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427811
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427812
Location:INTRON

Gene Symbol:NAV2
Accession:XM_011520444
Location:INTRON

Gene Symbol:NAV2
Accession:XM_024448758
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427809
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427822
Location:INTRON

Gene Symbol:NAV2
Accession:XM_011520450
Location:INTRON

Gene Symbol:NAV2
Accession:XM_017018520
Location:INTRON

Gene Symbol:NAV2
Accession:XM_017018524
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427829
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427836
Location:INTRON

Gene Symbol:NAV2
Accession:XM_006718364
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427821
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427834
Location:INTRON

Gene Symbol:NAV2
Accession:NM_182964
Location:INTRON

Gene Symbol:NAV2
Accession:XM_017018522
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427833
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427819
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427823
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427815
Location:INTRON

Gene Symbol:NAV2
Accession:XM_011520449
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427813
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427818
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427816
Location:INTRON

Gene Symbol:NAV2
Accession:XM_011520448
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427824
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427827
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427835
Location:INTRON

Gene Symbol:NAV2
Accession:XM_011520445
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427830
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427810
Location:INTRON

Gene Symbol:NAV2
Accession:XM_047427826
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV003394785 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene NAV2 CLINVAR
OMIM 607026 CLINVAR