rs17135115 Rat Genome Database

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Variant: rs17135115 -  Homo sapiens

RGD ID: 150499668
RS ID: rs17135115
ClinVar ID: CV1282891
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: AP5Z1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 7 4,820,581
GRCh38 7 4,780,950
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_1247t1:c.42-225T>C
NM_001364858.1:c.-240-225T>C
NM_014855.3:c.42-225T>C
LRG_1247:g.10320T>C
More... 		08/15/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:AP5Z1
Accession:NM_001364858
Location:5UTRS;INTRON

Gene Symbol:AP5Z1
Accession:NM_014855
Location:INTRON

Gene Symbol:AP5Z1
Accession:XM_047421098
Location:INTRON

Gene Symbol:AP5Z1
Accession:NR_157345
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001718232 CLINVAR
dbSNP (RS) rs17135115 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene AP5Z1 CLINVAR
OMIM 613653 CLINVAR