All of V1120

ID Consequence Gene/Location Detail Geno Type CHD Type
S2345 missense_variant MTHFR NM_005957.5:c.677T>C C/C isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2346 missense_variant MTHFR NM_005957.5:c.677T>C C/T isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2347 missense_variant MTHFR NM_005957.5:c.677T>C T/T isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2348 missense_variant MTHFR NM_005957.5:c.677T>C C/T+T/T isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2353 missense_variant MTHFR NM_005957.5:c.677T>C C/C isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2355 missense_variant MTHFR NM_005957.5:c.677T>C C/C isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2357 missense_variant MTHFR NM_005957.5:c.677T>C C/T isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2359 missense_variant MTHFR NM_005957.5:c.677T>C C/T isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2361 missense_variant MTHFR NM_005957.5:c.677T>C T/T isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2363 missense_variant MTHFR NM_005957.5:c.677T>C T/T isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2365 missense_variant MTHFR NM_005957.5:c.677T>C C/C isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2367 missense_variant MTHFR NM_005957.5:c.677T>C C/C isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2369 missense_variant MTHFR NM_005957.5:c.677T>C C/T isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2371 missense_variant MTHFR NM_005957.5:c.677T>C C/T isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2373 missense_variant MTHFR NM_005957.5:c.677T>C T/T isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S3416 missense_variant MTHFR NM_005957.5:c.677T>C C isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S3417 missense_variant MTHFR NM_005957.5:c.677T>C T isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA