RGD:14723215 Rat Genome Database

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Variant: RGD:14723215 -  Homo sapiens

RGD ID: 14723215
RS ID: rs59033408
ClinVar ID: CV670044
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: GCDH  
Reference Nucleotide: G
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 19 13,007,569
GRCh38 19 12,896,755
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_013976.5:c.853-155G>A
NM_000159.4:c.853-155G>A
NG_009292.1:g.10596G>A
NC_000019.10:g.12896755G>A
More... 		06/14/2018 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:GCDH
Accession:NM_000159
Location:INTRON

Gene Symbol:GCDH
Accession:NM_013976
Location:INTRON

Gene Symbol:GCDH
Accession:NR_102316
Location:INTRON;NON-CODING

Gene Symbol:GCDH
Accession:NR_102317
Location:INTRON;NON-CODING

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV000832432 CLINVAR
dbSNP (RS) rs59033408 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene GCDH CLINVAR
OMIM 608801 CLINVAR