RGD:11651767 Rat Genome Database

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Variant: RGD:11651767 -  Homo sapiens

RGD ID: 11651767
RS ID: rs886046747
ClinVar ID: CV309548
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: HABP2  NRAP  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 115,348,893
GRCh38 10 113,589,134
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_004132.5:c.*765C>T
NM_001322945.2:c.4981-55G>A
NG_008956.1:g.41116C>T
NC_000010.11:g.113589134C>T
More... 		01/13/2018 3 prime utr variant uncertain significance Factor vii-activating protease marburg i
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:HABP2
Accession:NM_001177660
Location:3UTRS;EXON

Gene Symbol:HABP2
Accession:NM_004132
Location:3UTRS;EXON

Gene Symbol:NRAP
Accession:XM_005269867
Location:INTRON

Gene Symbol:NRAP
Accession:XM_024448029
Location:INTRON

Gene Symbol:NRAP
Accession:NM_001261463
Location:INTRON

Gene Symbol:NRAP
Accession:XM_011539832
Location:INTRON

Gene Symbol:NRAP
Accession:XM_005269865
Location:INTRON

Gene Symbol:NRAP
Accession:XM_006717870
Location:INTRON

Gene Symbol:NRAP
Accession:NM_001322945
Location:INTRON

Gene Symbol:NRAP
Accession:NM_006175
Location:INTRON

Gene Symbol:NRAP
Accession:XM_047425253
Location:INTRON

Gene Symbol:NRAP
Accession:NM_198060
Location:INTRON

Gene Symbol:NRAP
Accession:XM_005269864
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000300970 CLINVAR
dbSNP (RS) rs886046747 CLINVAR
MedGen CN068943 CLINVAR
NCBI Gene HABP2 CLINVAR
  NRAP CLINVAR
OMIM 602873 CLINVAR
  603924 CLINVAR