RGD:405151735 Rat Genome Database

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Variant: RGD:405151735 -  Homo sapiens

RGD ID: 405151735
ClinVar ID: CV2950432
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KMT2A  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 11 118,343,980
GRCh38 11 118,473,265
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_613t1:c.2106T>C
NM_001197104.2:c.2106T>C
NM_005933.4:c.2106T>C
NM_001412597.1:c.2205T>C
More... 		01/04/2024 synonymous variant likely benign none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003670105 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KMT2A CLINVAR
OMIM 159555 CLINVAR