RGD:14716244 Rat Genome Database

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Variant: RGD:14716244 -  Homo sapiens

RGD ID: 14716244
RS ID: rs76834265
ClinVar ID: CV666457
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: FGD4  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 12 32,786,460
GRCh38 12 32,633,526
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_008626.2:g.238998T>G
NC_000012.11:g.32786460T>G
NM_139241.2:c.1762-23T>G
NM_001370297.1:c.1210-23T>G
More... 		06/20/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:FGD4
Accession:NM_001384128
Location:INTRON

Gene Symbol:FGD4
Accession:NM_001384130
Location:INTRON

Gene Symbol:FGD4
Accession:XM_011520558
Location:INTRON

Gene Symbol:FGD4
Accession:NM_001304484
Location:INTRON

Gene Symbol:FGD4
Accession:NM_001304481
Location:INTRON

Gene Symbol:FGD4
Accession:NM_001330374
Location:INTRON

Gene Symbol:FGD4
Accession:NM_001384132
Location:INTRON

Gene Symbol:FGD4
Accession:XM_047428291
Location:INTRON

Gene Symbol:FGD4
Accession:NM_001370298
Location:INTRON

Gene Symbol:FGD4
Accession:NM_001385118
Location:INTRON

Gene Symbol:FGD4
Accession:XM_047428292
Location:INTRON

Gene Symbol:FGD4
Accession:NM_001370297
Location:INTRON

Gene Symbol:FGD4
Accession:NM_001384127
Location:INTRON

Gene Symbol:FGD4
Accession:XM_047428294
Location:INTRON

Gene Symbol:FGD4
Accession:NM_001384131
Location:INTRON

Gene Symbol:FGD4
Accession:XM_005253310
Location:INTRON

Gene Symbol:FGD4
Accession:XM_011520559
Location:INTRON

Gene Symbol:FGD4
Accession:NM_001384126
Location:INTRON

Gene Symbol:FGD4
Accession:XM_047428293
Location:INTRON

Gene Symbol:FGD4
Accession:XM_047428295
Location:INTRON

Gene Symbol:FGD4
Accession:XM_047428296
Location:INTRON

Gene Symbol:FGD4
Accession:XM_047428297
Location:INTRON

Gene Symbol:FGD4
Accession:NM_139241
Location:INTRON

Gene Symbol:FGD4
Accession:NM_001304483
Location:INTRON

Gene Symbol:FGD4
Accession:NM_001330373
Location:INTRON

Gene Symbol:FGD4
Accession:NR_168884
Location:INTRON;NON-CODING

Gene Symbol:FGD4
Accession:XR_001748576
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000829663 CLINVAR
dbSNP (RS) rs76834265 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene FGD4 CLINVAR
OMIM 611104 CLINVAR