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Variant : CV511891 (NM_001197104.1(KMT2A):c.3790C>T (p.Arg1264Ter)) Homo sapiens

Symbol: CV511891
Name: NM_001197104.1(KMT2A):c.3790C>T (p.Arg1264Ter)
Condition: Inborn genetic diseases [RCV000622624]|not provided [RCV000760554]
Clinical Significance: pathogenic
Last Evaluated: 10/15/2018
Review Status: criteria provided, single submitter
Related Genes: KMT2A  
Variant Type: single nucleotide variant (SO:0001587)
Source: CLINVAR
Molecular Consequence: nonsense
Evidence: clinical testing
HGVS Name(s): NM_001197104.1:c.3790C>T
NC_000011.9:g.118352585C>T
LRG_613:g.50381C>T
LRG_613p1:p.Arg1264Ter
NG_027813.1:g.50381C>T
NC_000011.10:g.118481870C>T
NP_001184033.1:p.Arg1264Ter
LRG_613t1:c.3790C>T
NM_005933.4:c.3790C>T
NP_005924.2:p.Arg1264Ter
Position
Human AssemblyChrPosition (strand)Source
GRCh3811118,481,870 - 118,481,870CLINVAR
GRCh3711118,352,585 - 118,352,585CLINVAR
Cytogenetic Map1111q23.3CLINVAR



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13530599
Created: 2018-05-08
Species: Homo sapiens
Last Modified: 2020-09-22
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.