All of V2367

ID Consequence Gene/Location Detail Geno Type CHD Type
S4639 missense_variant DNMT1 NC_000019.10:g.10180505T>C T/T isolated CHD/non-isolated CHD: VSD/ASD/TOF/PDA/PAH/DORV/PS/AS/VSD, PFO/VSD, PFO, PAH/ASD, PAH/ASD, VSD, PAH/other
S4640 missense_variant DNMT1 NC_000019.10:g.10180505T>C C/T isolated CHD/non-isolated CHD: VSD/ASD/TOF/PDA/PAH/DORV/PS/AS/VSD, PFO/VSD, PFO, PAH/ASD, PAH/ASD, VSD, PAH/other
S4641 missense_variant DNMT1 NC_000019.10:g.10180505T>C C/C isolated CHD/non-isolated CHD: VSD/ASD/TOF/PDA/PAH/DORV/PS/AS/VSD, PFO/VSD, PFO, PAH/ASD, PAH/ASD, VSD, PAH/other
S4642 missense_variant DNMT1 NC_000019.10:g.10180505T>C C/T+C/C isolated CHD/non-isolated CHD: VSD/ASD/TOF/PDA/PAH/DORV/PS/AS/VSD, PFO/VSD, PFO, PAH/ASD, PAH/ASD, VSD, PAH/other
S4643 missense_variant DNMT1 NC_000019.10:g.10180505T>C C/T+T/T isolated CHD/non-isolated CHD: VSD/ASD/TOF/PDA/PAH/DORV/PS/AS/VSD, PFO/VSD, PFO, PAH/ASD, PAH/ASD, VSD, PAH/other
S4644 missense_variant DNMT1 NC_000019.10:g.10180505T>C T isolated CHD/non-isolated CHD: VSD/ASD/TOF/PDA/PAH/DORV/PS/AS/VSD, PFO/VSD, PFO, PAH/ASD, PAH/ASD, VSD, PAH/other
S4645 missense_variant DNMT1 NC_000019.10:g.10180505T>C C isolated CHD/non-isolated CHD: VSD/ASD/TOF/PDA/PAH/DORV/PS/AS/VSD, PFO/VSD, PFO, PAH/ASD, PAH/ASD, VSD, PAH/other