RGD:12841350 Rat Genome Database

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Variant: RGD:12841350 -  Homo sapiens

RGD ID: 12841350
RS ID: rs577925407
ClinVar ID: CV374704
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ACSF3  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 16 89,165,005
GRCh38 16 89,098,597
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001284316.2:c.-129-4007C>T
NG_031961.1:g.9789C>T
NC_000016.10:g.89098597C>T
NC_000016.9:g.89165005C>T
More... 		05/21/2018 5 prime utr variant|intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ACSF3
Accession:NM_174917
Location:5UTRS;EXON

Gene Symbol:ACSF3
Accession:NM_001243279
Location:5UTRS;EXON

Gene Symbol:
Accession:
Location:5UTRS;EXON

Gene Symbol:
Accession:
Location:5UTRS;EXON

Gene Symbol:
Accession:
Location:5UTRS;EXON

Gene Symbol:
Accession:
Location:5UTRS;EXON

Gene Symbol:
Accession:
Location:5UTRS;EXON

Gene Symbol:
Accession:
Location:5UTRS;EXON

Gene Symbol:
Accession:
Location:5UTRS;EXON

Gene Symbol:
Accession:
Location:5UTRS;EXON

Gene Symbol:
Accession:
Location:5UTRS;EXON

Gene Symbol:ACSF3
Accession:NM_001127214
Location:5UTRS;INTRON

Gene Symbol:ACSF3
Accession:NM_001284316
Location:5UTRS;INTRON

Gene Symbol:
Accession:
Location:5UTRS;INTRON

Gene Symbol:
Accession:
Location:5UTRS;INTRON

Gene Symbol:
Accession:
Location:5UTRS;INTRON

Gene Symbol:
Accession:
Location:5UTRS;INTRON

Gene Symbol:
Accession:
Location:5UTRS;INTRON

Gene Symbol:ACSF3
Accession:NR_104293
Location:EXON;NON-CODING

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

Gene Symbol:ACSF3
Accession:NR_147928
Location:EXON;NON-CODING

Gene Symbol:ACSF3
Accession:NR_147929
Location:EXON;NON-CODING

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

Gene Symbol:ACSF3
Accession:NR_045667
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001703764 CLINVAR
dbSNP (RS) rs577925407 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ACSF3 CLINVAR
OMIM 614245 CLINVAR