RGD:14735983 Rat Genome Database

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Variant: RGD:14735983 -  Homo sapiens

RGD ID: 14735983
RS ID: rs13057374
ClinVar ID: CV669510
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TXNRD2  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 22 19,871,097
GRCh38 22 19,883,574
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001352302.2:c.662-113G>C
NM_001352301.2:c.860-113G>C
NM_001352300.2:c.947-113G>C
NM_006440.5:c.950-113G>C
More... 		06/18/2018 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TXNRD2
Accession:NM_006440
Location:INTRON

Gene Symbol:TXNRD2
Accession:NM_001282512
Location:INTRON

Gene Symbol:TXNRD2
Accession:NM_001352302
Location:INTRON

Gene Symbol:TXNRD2
Accession:NM_001352303
Location:INTRON

Gene Symbol:TXNRD2
Accession:NM_001352300
Location:INTRON

Gene Symbol:TXNRD2
Accession:NM_001352301
Location:INTRON

Gene Symbol:TXNRD2
Accession:NR_147957
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000838265 CLINVAR
dbSNP (RS) rs13057374 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TXNRD2 CLINVAR
OMIM 606448 CLINVAR