RGD:13525735 Rat Genome Database

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Variant: RGD:13525735 -  Homo sapiens

RGD ID: 13525735
RS ID: rs199582237
ClinVar ID: CV507821
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SSR4  
Reference Nucleotide: A
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 X 153,063,513
GRCh38 X 153,798,058
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_041795.1:g.8884A>G
NC_000023.11:g.153798058A>G
NC_000023.10:g.153063513A>G
NM_001204527.2:c.376-13A>G
More... 		12/15/2021 intron variant benign|likely benign AllHighlyPenetrant; none provided

Variant Details
Variant Transcripts
Gene Symbol:SSR4
Accession:XM_047442390
Location:INTRON

Gene Symbol:SSR4
Accession:XM_047442389
Location:INTRON

Gene Symbol:SSR4
Accession:NM_001204526
Location:INTRON

Gene Symbol:SSR4
Accession:NM_001204527
Location:INTRON

Gene Symbol:SSR4
Accession:NM_006280
Location:INTRON

Gene Symbol:SSR4
Accession:NR_037927
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000603400 CLINVAR
  RCV002066873 CLINVAR
dbSNP (RS) rs199582237 CLINVAR
MedGen C3661900 CLINVAR
  CN169374 CLINVAR
NCBI Gene SSR4 CLINVAR
OMIM 300090 CLINVAR