RGD:152064453 Rat Genome Database

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Variant: RGD:152064453 -  Homo sapiens

RGD ID: 152064453
RS ID: rs373431345
ClinVar ID: CV1535805
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: TGM1  
Reference Nucleotide: G
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 14 24,723,499
GRCh38 14 24,254,293
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_000359.3:c.2089-5C>G
NG_007150.2:g.13874C>G
NC_000014.9:g.24254293G>C
NC_000014.8:g.24723499G>C
More... 		10/21/2021 intron variant likely benign none provided

Variant Details
Variant Transcripts
Gene Symbol:TGM1
Accession:NM_000359
Location:INTRON

Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV002168440 CLINVAR
dbSNP (RS) rs373431345 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene TGM1 CLINVAR
OMIM 190195 CLINVAR