rs201603249 Rat Genome Database

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Variant: rs201603249 -  Homo sapiens

RGD ID: 15102185
RS ID: rs201603249
ClinVar ID: CV729924
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: YY1AP1  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 1 155,646,332
GRCh38 1 155,676,541
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_139119.3:c.324+7C>T
NM_001198900.2:c.291+7C>T
NM_001198906.2:c.522+7C>T
NM_139118.3:c.522+7C>T
More... 		08/01/2024 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:YY1AP1
Accession:NM_001198906
Location:INTRON

Gene Symbol:YY1AP1
Accession:NM_018253
Location:INTRON

Gene Symbol:YY1AP1
Accession:NM_139119
Location:INTRON

Gene Symbol:YY1AP1
Accession:NM_001198900
Location:INTRON

Gene Symbol:YY1AP1
Accession:NM_001198901
Location:INTRON

Gene Symbol:YY1AP1
Accession:NM_139118
Location:INTRON

Gene Symbol:YY1AP1
Accession:NM_001198902
Location:INTRON

Gene Symbol:YY1AP1
Accession:NM_001198905
Location:INTRON

Gene Symbol:YY1AP1
Accession:NM_001198903
Location:INTRON

Gene Symbol:YY1AP1
Accession:NM_139121
Location:INTRON

Gene Symbol:YY1AP1
Accession:NM_001198904
Location:INTRON

Gene Symbol:YY1AP1
Accession:NM_001198899
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000892430 CLINVAR
dbSNP (RS) rs201603249 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene YY1AP1 CLINVAR
OMIM 607860 CLINVAR