RGD:405123068 Rat Genome Database

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Variant: RGD:405123068 -  Homo sapiens

RGD ID: 405123068
ClinVar ID: CV3020985
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KMT2A  
Reference Nucleotide: C
Variant Nucleotide: A
Position
Assembly Chr Position
GRCh37 11 118,373,226
GRCh38 11 118,502,511
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_613t1:c.6619C>A
NM_005933.4:c.6610C>A
NM_001197104.2:c.6619C>A
NM_001412597.1:c.6709C>A
More... 		03/02/2023 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003700967 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KMT2A CLINVAR
OMIM 159555 CLINVAR