RGD:15161719 Rat Genome Database

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Variant: RGD:15161719 -  Homo sapiens

RGD ID: 15161719
RS ID: rs143086637
ClinVar ID: CV731145
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: LOC127886579  ZNHIT3  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 17 34,842,638
GRCh38 17 36,486,794
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001281433.2:c.86+9G>A
NM_001281434.2:c.86+9G>A
NM_001281432.2:c.86+9G>A
NM_004773.3:c.86+9G>A
More... 		02/06/2019 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ZNHIT3
Accession:NM_001281434
Location:INTRON

Gene Symbol:ZNHIT3
Accession:NM_001281432
Location:INTRON

Gene Symbol:ZNHIT3
Accession:NM_004773
Location:INTRON

Gene Symbol:ZNHIT3
Accession:NM_001281433
Location:INTRON

Gene Symbol:ZNHIT3
Accession:NR_104010
Location:INTRON;NON-CODING

Gene Symbol:ZNHIT3
Accession:NR_104009
Location:INTRON;NON-CODING

Gene Symbol:ZNHIT3
Accession:NR_104011
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000881622 CLINVAR
dbSNP (RS) rs143086637 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ZNHIT3 CLINVAR
OMIM 604500 CLINVAR