rs2019740042 Rat Genome Database

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Variant: rs2019740042 -  Homo sapiens

RGD ID: 152155806
RS ID: rs2019740042
ClinVar ID: CV1561030
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ZNF341  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 20 32,369,200
GRCh38 20 33,781,394
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001282935.2:c.1449+7G>T
NM_032819.5:c.1698+7G>T
NM_001282933.2:c.1719+7G>T
NG_053072.1:g.54635G>T
More... 		06/27/2022 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:ZNF341
Accession:NM_032819
Location:INTRON

Gene Symbol:ZNF341
Accession:NM_001282933
Location:INTRON

Gene Symbol:ZNF341
Accession:NM_001282935
Location:INTRON

Gene Symbol:ZNF341
Accession:NR_104259
Location:INTRON;NON-CODING

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002102914 CLINVAR
dbSNP (RS) rs2019740042 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene ZNF341 CLINVAR
OMIM 618269 CLINVAR