RGD:11660357 Rat Genome Database

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Variant: RGD:11660357 -  Homo sapiens

RGD ID: 11660357
RS ID: rs886047531
ClinVar ID: CV324192
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ZFYVE27  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 99,520,340
GRCh38 10 97,760,583
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_017075.1:g.28463C>T
NC_000010.11:g.97760583C>T
NC_000010.10:g.99520340C>T
NR_169797.1:n.2480C>T
More... 		01/13/2018 3 prime utr variant uncertain significance Spastic paraplegia 33, autosomal dominant
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:ZFYVE27
Accession:NM_001002261
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001174119
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001174121
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385911
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385906
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385891
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385877
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385886
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385881
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385893
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385885
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385888
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385887
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385904
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385905
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385918
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001174120
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001174122
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385890
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385894
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385871
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385908
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385915
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385889
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385902
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385875
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385880
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385919
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_144588
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001002262
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385876
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385895
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385900
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385916
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385898
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385903
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385899
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385897
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385901
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385892
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385879
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385878
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NM_001385896
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:XM_047424567
Location:3UTRS;EXON

Gene Symbol:ZFYVE27
Accession:NR_169809
Location:EXON;NON-CODING

Gene Symbol:ZFYVE27
Accession:NR_169802
Location:EXON;NON-CODING

Gene Symbol:ZFYVE27
Accession:NR_169799
Location:EXON;NON-CODING

Gene Symbol:ZFYVE27
Accession:NR_169797
Location:EXON;NON-CODING

Gene Symbol:ZFYVE27
Accession:NR_169794
Location:EXON;NON-CODING

Gene Symbol:ZFYVE27
Accession:NR_169811
Location:EXON;NON-CODING

Gene Symbol:ZFYVE27
Accession:NR_169804
Location:EXON;NON-CODING

Gene Symbol:ZFYVE27
Accession:NR_169806
Location:EXON;NON-CODING

Gene Symbol:ZFYVE27
Accession:NR_169803
Location:EXON;NON-CODING

Gene Symbol:ZFYVE27
Accession:NR_169801
Location:EXON;NON-CODING

Gene Symbol:ZFYVE27
Accession:NR_169810
Location:EXON;NON-CODING

Gene Symbol:ZFYVE27
Accession:NR_169808
Location:EXON;NON-CODING

Gene Symbol:ZFYVE27
Accession:NR_169798
Location:EXON;NON-CODING

Gene Symbol:ZFYVE27
Accession:NR_169805
Location:EXON;NON-CODING

Gene Symbol:ZFYVE27
Accession:NR_169795
Location:EXON;NON-CODING

Gene Symbol:ZFYVE27
Accession:NR_169796
Location:EXON;NON-CODING

Gene Symbol:ZFYVE27
Accession:NR_169800
Location:EXON;NON-CODING

Gene Symbol:ZFYVE27
Accession:NM_001385882
Location:INTRON

Gene Symbol:ZFYVE27
Accession:NM_001385883
Location:INTRON

Gene Symbol:ZFYVE27
Accession:XM_017015644
Location:INTRON

Gene Symbol:ZFYVE27
Accession:XM_011539253
Location:INTRON

Gene Symbol:ZFYVE27
Accession:XM_017015645
Location:INTRON

Gene Symbol:ZFYVE27
Accession:NM_001385884
Location:INTRON

Gene Symbol:ZFYVE27
Accession:XM_011539252
Location:INTRON

Gene Symbol:ZFYVE27
Accession:XM_017015646
Location:INTRON

Gene Symbol:ZFYVE27
Accession:XR_945594
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000366072 CLINVAR
dbSNP (RS) rs886047531 CLINVAR
MedGen C1853251 CLINVAR
NCBI Gene ZFYVE27 CLINVAR
OMIM 610243 CLINVAR
  610244 CLINVAR