RGD:126909064 Rat Genome Database

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Variant: RGD:126909064 -  Homo sapiens

RGD ID: 126909064
RS ID: rs1475452583
ClinVar ID: CV1053084
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SNX14  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 6 86,246,650
GRCh38 6 85,536,932
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001350545.2:c.1032-8A>G
NM_001350546.2:c.1032-8A>G
NM_001350544.2:c.1176-8A>G
NM_001350532.1:c.1539-8A>G
More... 		02/18/2020 intron variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:SNX14
Accession:XM_047419123
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350551
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350543
Location:INTRON

Gene Symbol:SNX14
Accession:XM_047419125
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350539
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350546
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350553
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350550
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350549
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350533
Location:INTRON

Gene Symbol:SNX14
Accession:NM_020468
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350552
Location:INTRON

Gene Symbol:SNX14
Accession:XM_047419127
Location:INTRON

Gene Symbol:SNX14
Accession:XM_047419121
Location:INTRON

Gene Symbol:SNX14
Accession:XM_047419129
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350547
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350536
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350532
Location:INTRON

Gene Symbol:SNX14
Accession:NM_153816
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001297614
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350545
Location:INTRON

Gene Symbol:SNX14
Accession:XM_047419128
Location:INTRON

Gene Symbol:SNX14
Accession:XM_017011090
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350544
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350542
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350548
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350538
Location:INTRON

Gene Symbol:SNX14
Accession:XM_047419126
Location:INTRON

Gene Symbol:SNX14
Accession:XM_047419122
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350540
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001304479
Location:INTRON

Gene Symbol:SNX14
Accession:XM_047419120
Location:INTRON

Gene Symbol:SNX14
Accession:XM_047419124
Location:INTRON

Gene Symbol:SNX14
Accession:XM_011535977
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350534
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350537
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350535
Location:INTRON

Gene Symbol:SNX14
Accession:NM_001350541
Location:INTRON

Gene Symbol:SNX14
Accession:NR_146776
Location:INTRON;NON-CODING

Gene Symbol:SNX14
Accession:NR_146778
Location:INTRON;NON-CODING

Gene Symbol:SNX14
Accession:NR_146774
Location:INTRON;NON-CODING

Gene Symbol:SNX14
Accession:NR_146779
Location:INTRON;NON-CODING

Gene Symbol:SNX14
Accession:NR_146775
Location:INTRON;NON-CODING

Gene Symbol:SNX14
Accession:NR_146777
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:25741868  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001374928 CLINVAR
dbSNP (RS) rs1475452583 CLINVAR
MedGen C1535926 CLINVAR
NCBI Gene SNX14 CLINVAR
OMIM 616105 CLINVAR