RGD:405190440 Rat Genome Database

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Variant: RGD:405190440 -  Homo sapiens

RGD ID: 405190440
ClinVar ID: CV2874956
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KMT2A  TTC36-AS1  
Reference Nucleotide: A
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 11 118,392,649
GRCh38 11 118,521,934
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
LRG_613t1:c.11681A>T
NM_005933.4:c.11672A>T
NM_001197104.2:c.11681A>T
NM_001412597.1:c.11771A>T
More... 		01/25/2024 missense variant uncertain significance none provided

Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003550253 CLINVAR
MedGen C3661900 CLINVAR
NCBI Gene KMT2A CLINVAR
  TTC36-AS1 CLINVAR
OMIM 159555 CLINVAR