RGD:405128697 Rat Genome Database

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Variant: RGD:405128697 -  Homo sapiens

RGD ID: 405128697
ClinVar ID: CV2962368
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: KMT2D  
Reference Nucleotide: C
Variant Nucleotide: T
Position
Assembly Chr Position
GRCh37 12 49,444,829
GRCh38 12 49,051,046
JBrowse: View Region in Genome Browser (JBrowse)
Model



ClinVar Data
HGVS Name(s) Last Evaluated Molecular Consequence Clinical Significance Trait Synonyms
NG_027827.1:g.9279G>A
NC_000012.12:g.49051046C>T
NC_000012.11:g.49444829C>T
NM_003482.3:c.2637G>A
More... 		08/17/2023 synonymous variant benign Kabuki make-up syndrome; Niikawa-Kuroki syndrome
Disease Annotations     Click to see Annotation Detail View


Variant Details
Variant Samples
Additional References at PubMed
PMID:28492532  


Additional Information

Database Acc Id Source(s)
ClinVar RCV003753941 CLINVAR
MedGen C0796004 CLINVAR
NCBI Gene KMT2D CLINVAR
OMIM 147920 CLINVAR
  602113 CLINVAR
SNOMED CT 313426007 CLINVAR