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DOT1L c.2802C>G ;(p.P934=)
Variant ID: 19-2220217-C-G
NM_032482.2(
DOT1L
):c.2802C>G;(p.P934=)
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
De novo mutations in moderate or severe intellectual disability.
Plos Genetics
Hamdan, Fadi F FF; Srour, Myriam M; Capo-Chichi, Jose-Mario JM; Daoud, Hussein H; Nassif, Christina C; Patry, Lysanne L; Massicotte, Christine C; Ambalavanan, Amirthagowri A; Spiegelman, Dan D; Diallo, Ousmane O; Henrion, Edouard E; Dionne-Laporte, Alexandre A; Fougerat, Anne A; Pshezhetsky, Alexey V AV; Venkateswaran, Sunita S; Rouleau, Guy A GA; Michaud, Jacques L JL
Publication Date: 2014-10
Variant appearance in text: DOT1L: P934P
PubMed Link:
25356899
Variant Present in the following documents:
pgen.1004772.s004.xlsx, sheet 35
View BVdb publication page