RGD:15114793 Rat Genome Database

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Variant: RGD:15114793 -  Homo sapiens

RGD ID: 15114793
RS ID: rs77238980
ClinVar ID: CV779378
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CD109  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 6 74,495,203
GRCh38 6 73,785,480
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001159588.3:c.2106+3A>G
NM_001159587.3:c.2337+3A>G
NM_133493.4:c.2337+3A>G
LRG_1002:g.94696A>G
More... 		05/14/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CD109
Accession:XM_047418212
Location:INTRON

Gene Symbol:CD109
Accession:NM_001159588
Location:INTRON

Gene Symbol:CD109
Accession:XM_047418215
Location:INTRON

Gene Symbol:CD109
Accession:XM_047418217
Location:INTRON

Gene Symbol:CD109
Accession:XM_047418214
Location:INTRON

Gene Symbol:CD109
Accession:XM_047418213
Location:INTRON

Gene Symbol:CD109
Accession:XM_047418211
Location:INTRON

Gene Symbol:CD109
Accession:XM_047418216
Location:INTRON

Gene Symbol:CD109
Accession:NM_001159587
Location:INTRON

Gene Symbol:CD109
Accession:NM_133493
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000961740 CLINVAR
dbSNP (RS) rs77238980 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene CD109 CLINVAR
OMIM 608859 CLINVAR