All of V0054

ID Consequence Gene/Location Detail Geno Type CHD Type
S0183 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G isolated CHD: TOF
S0184 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G isolated CHD: TOF
S0185 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G isolated CHD: TOF
S0186 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/A isolated CHD: TOF
S0187 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/A isolated CHD: TOF
S0188 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/A isolated CHD: TOF
S0189 missense_variant MTHFD1 NM_001364837.1:c.1958G>A A/A isolated CHD: TOF
S0190 missense_variant MTHFD1 NM_001364837.1:c.1958G>A A/A isolated CHD: TOF
S0191 missense_variant MTHFD1 NM_001364837.1:c.1958G>A A/A isolated CHD: TOF
S0192 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G isolated CHD: TOF
S0193 missense_variant MTHFD1 NM_001364837.1:c.1958G>A A isolated CHD: TOF
S0211 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G and G/G(father and mother) isolated CHD: TOF
S0212 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G and G/A(or A/A)(father and mother) isolated CHD: TOF
S0213 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/A and G/A(or A/A)(father and mother) isolated CHD: TOF
S0214 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/A and G/A(or A/A)+G/G and G/A(or A/A)(father and mother) isolated CHD: TOF
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