RGD:408367230 Rat Genome Database

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Variant: RGD:408367230 -  Homo sapiens

RGD ID: 408367230
ClinVar ID: CV3517036
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: COL25A1  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 4 109,738,589
GRCh38 4 108,817,433
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_198721.4:c.1926G>T
NG_047204.1:g.490320G>T
NC_000004.12:g.108817433C>A
NC_000004.11:g.109738589C>A
More... 		09/11/2019 non-coding transcript variant likely benign COL25A1-related condition

Variant Details
Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV004757917 CLINVAR
NCBI Gene COL25A1 CLINVAR
OMIM 610004 CLINVAR