RGD:12742295 Rat Genome Database

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Variant: RGD:12742295 -  Homo sapiens

RGD ID: 12742295
RS ID: rs1057518208
ClinVar ID: CV359851
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ADAM9  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 8 38,869,176
GRCh38 8 39,011,657
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.19672G>A
NC_000008.11:g.39011657G>A
NC_000008.10:g.38869176G>A
NM_003816.2:c.196-1G>A
More... 		11/03/2016 splice acceptor variant pathogenic none provided

Variant Details
Variant Transcripts
Gene Symbol:ADAM9
Accession:XM_047422390
Location:INTRON

Gene Symbol:ADAM9
Accession:XM_011544682
Location:INTRON

Gene Symbol:ADAM9
Accession:NM_003816
Location:INTRON

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

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

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000413336 CLINVAR
dbSNP (RS) rs1057518208 CLINVAR
MedGen CN517202 CLINVAR
NCBI Gene ADAM9 CLINVAR
OMIM 602713 CLINVAR