All of V1121

ID Consequence Gene/Location Detail Geno Type CHD Type
S2349 missense_variant MTHFR NM_005957.5:c.1298A>C A/A isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2350 missense_variant MTHFR NM_005957.5:c.1298A>C A/C isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2354 missense_variant MTHFR NM_005957.5:c.1298A>C A/A isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2356 missense_variant MTHFR NM_005957.5:c.1298A>C A/C isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2358 missense_variant MTHFR NM_005957.5:c.1298A>C A/A isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2360 missense_variant MTHFR NM_005957.5:c.1298A>C A/C isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2362 missense_variant MTHFR NM_005957.5:c.1298A>C A/A isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2364 missense_variant MTHFR NM_005957.5:c.1298A>C A/C isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2375 missense_variant MTHFR NM_005957.5:c.1298A>C A/A isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2377 missense_variant MTHFR NM_005957.5:c.1298A>C A/A isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2379 missense_variant MTHFR NM_005957.5:c.1298A>C A/C isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2381 missense_variant MTHFR NM_005957.5:c.1298A>C A/C isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S3418 missense_variant MTHFR NM_005957.5:c.1298A>C A isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S3419 missense_variant MTHFR NM_005957.5:c.1298A>C C isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA