RGD:11605388 Rat Genome Database

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Variant: RGD:11605388 -  Homo sapiens

RGD ID: 11605388
RS ID: rs763045109
ClinVar ID: CV314247
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ADAM9  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 8 38,961,351
GRCh38 8 39,103,832
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_016335.1:g.111847C>T
NC_000008.11:g.39103832C>T
NC_000008.10:g.38961351C>T
NR_027878.2:n.2577C>T
More...
06/14/2016 3 prime utr variant uncertain significance
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Transcripts
Gene Symbol:ADAM9
Accession:NM_003816
Location:3UTRS;EXON

Gene Symbol:ADAM9
Accession:XM_011544682
Location:3UTRS;EXON

Gene Symbol:ADAM9
Accession:NR_027638
Location:EXON;NON-CODING

Gene Symbol:ADAM9
Accession:NR_027878
Location:EXON;NON-CODING

Gene Symbol:ADAM9
Accession:NR_027639
Location:EXON;NON-CODING

Gene Symbol:ADAM9
Accession:XM_047422390
Location:INTRON

Gene Symbol:ADAM9
Accession:XR_007060759
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000319035 CLINVAR
dbSNP (RS) rs763045109 CLINVAR
MedGen C1423873 CLINVAR
NCBI Gene ADAM9 CLINVAR
OMIM 602713 CLINVAR
  612775 CLINVAR