RGD:13803954 Rat Genome Database

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Variant: RGD:13803954 -  Homo sapiens

RGD ID: 13803954
RS ID: rs1569491107
ClinVar ID: CV578099
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL4A5  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 X 107,824,258
GRCh38 X 108,581,028
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000495.5:c.936+1G>A
NC_000023.11:g.108581028G>A
LRG_232:g.146105G>A
NC_000023.10:g.107824258G>A
More... 		03/03/2020 splice donor variant pathogenic|likely pathogenic none provided

Variant Details
Variant Transcripts
Gene Symbol:COL4A5
Accession:NM_000495
Location:INTRON

Gene Symbol:COL4A5
Accession:NM_033380
Location:INTRON

Gene Symbol:COL4A5
Accession:XM_017029262
Location:INTRON

Gene Symbol:COL4A5
Accession:XM_011530849
Location:INTRON

Gene Symbol:COL4A5
Accession:XM_047441811
Location:INTRON

Gene Symbol:COL4A5
Accession:XM_017029260
Location:INTRON

Gene Symbol:COL4A5
Accession:XM_047441810
Location:INTRON

Gene Symbol:COL4A5
Accession:XM_017029261
Location:INTRON

Gene Symbol:COL4A5
Accession:XM_017029259
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:9195222   PMID:10752524   PMID:14514738   PMID:16199547   PMID:24854265   PMID:26809805   PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV001379652 CLINVAR
dbSNP (RS) rs1569491107 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene COL4A5 CLINVAR
OMIM 303630 CLINVAR