rs17880345 Rat Genome Database

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Variant: rs17880345 -  Homo sapiens

RGD ID: 15159458
RS ID: rs17880345
ClinVar ID: CV777808
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: AS3MT  BORCS7-ASMT  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 104,629,831
GRCh38 10 102,870,074
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_020682.4:c.43-10G>T
NC_000010.11:g.102870074G>T
NC_000010.10:g.104629831G>T
NM_020682.3:c.43-10G>T
 07/05/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:CYT19
Accession:NM_020682
Location:INTRON

Gene Symbol:BORCS7-ASMT
Accession:NR_037644
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV000947280 CLINVAR
dbSNP (RS) rs17880345 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene AS3MT CLINVAR
  BORCS7-ASMT CLINVAR
OMIM 611806 CLINVAR