RGD:150548293 Rat Genome Database

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Variant: RGD:150548293 -  Homo sapiens

RGD ID: 150548293
RS ID: rs76187771
ClinVar ID: CV1316197
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC16A12  
Reference Nucleotide: G
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 10 91,203,478
GRCh38 10 89,443,721
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_213606.4:c.304+35C>A
NG_021179.1:g.96836C>A
NC_000010.11:g.89443721G>T
NC_000010.10:g.91203478G>T
 05/16/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:SLC16A12
Accession:XM_017016238
Location:INTRON

Gene Symbol:SLC16A12
Accession:XM_047425223
Location:INTRON

Gene Symbol:SLC16A12
Accession:XM_047425221
Location:INTRON

Gene Symbol:SLC16A12
Accession:XM_047425222
Location:INTRON

Gene Symbol:SLC16A12
Accession:NM_213606
Location:INTRON

Gene Symbol:SLC16A12
Accession:XM_017016239
Location:INTRON

Gene Symbol:SLC16A12
Accession:XM_017016237
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001785998 CLINVAR
dbSNP (RS) rs76187771 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene SLC16A12 CLINVAR
OMIM 611910 CLINVAR