RGD:13525817 Rat Genome Database

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Variant: RGD:13525817 -  Homo sapiens

RGD ID: 13525817
RS ID: rs147388951
ClinVar ID: CV504200
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: CSRP3-AS1  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 19,223,542
GRCh38 11 19,201,995
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Clinical Significance Trait Synonyms
LRG_440:g.13579C>T
NG_011932.2:g.13579C>T
NM_003476.3:c.-70C>T
NC_000011.10:g.19201995G>A
More... 		09/12/2017 likely benign AllHighlyPenetrant

Variant Details
Variant Transcripts
Gene Symbol:CSRP3-AS1
Accession:NR_183673
Location:INTRON;NON-CODING

Gene Symbol:CSRP3-AS1
Accession:NR_183672
Location:INTRON;NON-CODING

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

Gene Symbol:CSRP3-AS1
Accession:NR_183675
Location:INTRON;NON-CODING

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

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

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000603470 CLINVAR
dbSNP (RS) rs147388951 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene CSRP3 CLINVAR
  CSRP3-AS1 CLINVAR
OMIM 600824 CLINVAR