RGD:8654080 Rat Genome Database

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Variant: RGD:8654080 -  Homo sapiens

RGD ID: 8654080
ClinVar ID: CV130655
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: SLC16A7  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 60,051,894
GRCh38 12 59,658,113
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NC_000012.12:g.59658113C>T
NC_000012.11:g.60051894C>T
NM_001270622.1:c.-11+2863C>T
 intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:SLC16A7
Accession:NM_001270623
Location:5UTRS;INTRON

Gene Symbol:SLC16A7
Accession:NM_001270622
Location:5UTRS;INTRON

Gene Symbol:SLC16A7
Accession:XM_011538989
Location:5UTRS;INTRON

Gene Symbol:SLC16A7
Accession:XM_047429885
Location:INTRON

Gene Symbol:SLC16A7
Accession:XM_011538992
Location:INTRON

Gene Symbol:SLC16A7
Accession:XM_011538991
Location:INTRON

Gene Symbol:SLC16A7
Accession:NM_004731
Location:INTRON

Gene Symbol:SLC16A7
Accession:XM_005269231
Location:INTRON

Gene Symbol:SLC16A7
Accession:XM_011538995
Location:INTRON

Gene Symbol:SLC16A7
Accession:XM_017020226
Location:INTRON

Gene Symbol:SLC16A7
Accession:XM_024449276
Location:INTRON

Gene Symbol:SLC16A7
Accession:XM_011538990
Location:INTRON

Gene Symbol:SLC16A7
Accession:NR_073055
Location:INTRON;NON-CODING

Gene Symbol:SLC16A7
Accession:NR_073056
Location:INTRON;NON-CODING

Variant Samples