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Table 3 NCOR1 variants observed during the validation by Sanger sequencing method. The variants of G207C and C241T present only in VSD cases. G244A present in three TOF cases as well

From: Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defects

Chromosome position Variants VSD and TOF cases (26) Control (10)
17: 16068377-16068377 G207C 4/26 (15.35%) Nil
17: 16068343-16068343 C241T 5/26 (19.2%)
17: 16068340-16068340 G244A 12/26 (46.1%)