All of V1122

ID Consequence Gene/Location Detail Geno Type CHD Type
S2351 missense_variant MTHFR NM_005957.5:c.1793G>A G/G isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2352 missense_variant MTHFR NM_005957.5:c.1793G>A G/A isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2366 missense_variant MTHFR NM_005957.5:c.1793G>A G/G isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2368 missense_variant MTHFR NM_005957.5:c.1793G>A G/A isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2370 missense_variant MTHFR NM_005957.5:c.1793G>A G/G isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2372 missense_variant MTHFR NM_005957.5:c.1793G>A G/A isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2374 missense_variant MTHFR NM_005957.5:c.1793G>A G/G isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2376 missense_variant MTHFR NM_005957.5:c.1793G>A G/G isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2378 missense_variant MTHFR NM_005957.5:c.1793G>A G/A isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2380 missense_variant MTHFR NM_005957.5:c.1793G>A G/G isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S2382 missense_variant MTHFR NM_005957.5:c.1793G>A G/A isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S3420 missense_variant MTHFR NM_005957.5:c.1793G>A G isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA
S3421 missense_variant MTHFR NM_005957.5:c.1793G>A A isolated CHD: VSD/ASD/PDA/TOF/TGA/PTA

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