RGD:150536774 Rat Genome Database

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Variant: RGD:150536774 -  Homo sapiens

RGD ID: 150536774
ClinVar ID: CV1314270
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: C19orf12  
Reference Nucleotide: T
Variant Nucleotide: G
Position
Assembly Chr Position
GRCh37 19 30,193,886
GRCh38 19 29,702,979
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_001256046.3:c.161-2A>C
NM_001256047.2:c.161-2A>C
NM_031448.6:c.161-2A>C
NC_000019.10:g.29702979T>G
More... 		09/30/2019 splice acceptor variant likely pathogenic none provided

Variant Details
Variant Transcripts
Gene Symbol:C19orf12
Accession:NM_001282931
Location:5UTRS;INTRON

Gene Symbol:C19orf12
Accession:NM_001282930
Location:5UTRS;INTRON

Gene Symbol:C19orf12
Accession:NM_001282929
Location:5UTRS;INTRON

Gene Symbol:C19orf12
Accession:XM_047439497
Location:5UTRS;INTRON

Gene Symbol:C19orf12
Accession:NM_001256047
Location:INTRON

Gene Symbol:C19orf12
Accession:NM_001256046
Location:INTRON

Gene Symbol:C19orf12
Accession:NM_001031726
Location:INTRON

Gene Symbol:C19orf12
Accession:XM_047439496
Location:INTRON

Gene Symbol:C19orf12
Accession:XM_024451735
Location:INTRON

Gene Symbol:C19orf12
Accession:NM_031448
Location:INTRON

Gene Symbol:C19orf12
Accession:XM_024451734
Location:INTRON

Variant Samples