RGD:8654019 Rat Genome Database

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Variant: RGD:8654019 -  Homo sapiens

RGD ID: 8654019
ClinVar ID: CV130594
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: ANO6  LOC105369743  
Reference Nucleotide: C
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 12 45,788,288
GRCh38 12 45,394,505
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001142679.1:c.1386+4007C>G
NG_028220.1:g.183519C>G
NC_000012.12:g.45394505C>G
NC_000012.11:g.45788288C>G
More... 		intron|intron variant uncertain significance Lung cancer, somatic

Variant Details
Variant Transcripts
Gene Symbol:ANO6
Accession:NM_001142679
Location:INTRON

Gene Symbol:ANO6
Accession:NM_001025356
Location:INTRON

Gene Symbol:ANO6
Accession:NM_001142678
Location:INTRON

Gene Symbol:ANO6
Accession:NM_001204803
Location:INTRON

Gene Symbol:ANO6
Accession:XM_005268707
Location:INTRON

Gene Symbol:
Accession:
Location:INTRON

Gene Symbol:ANO6
Accession:NM_001410973
Location:INTRON

Gene Symbol:LOC105369743
Accession:XR_944886
Location:INTRON;NON-CODING

Gene Symbol:LOC105369743
Accession:XR_944887
Location:INTRON;NON-CODING

Variant Samples