RGD:150487839 Rat Genome Database

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Variant: RGD:150487839 -  Homo sapiens

RGD ID: 150487839
RS ID: rs78356340
ClinVar ID: CV1251583
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: MMP13  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 102,819,916
GRCh38 11 102,949,187
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NM_002427.4:c.918-29C>T
NG_021404.1:g.11548C>T
NC_000011.10:g.102949187G>A
NC_000011.9:g.102819916G>A
 05/25/2020 intron variant benign none provided

Variant Details
Variant Transcripts
Gene Symbol:MMP13
Accession:NM_002427
Location:INTRON

Variant Samples

Additional Information

Database Acc Id Source(s)
ClinVar RCV001674254 CLINVAR
dbSNP (RS) rs78356340 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene MMP13 CLINVAR
OMIM 600108 CLINVAR