All of V0053

ID Consequence Gene/Location Detail Geno Type CHD Type
S0172 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G isolated CHD: PAD
S0173 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G isolated CHD: PAD
S0174 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G isolated CHD: PAD
S0175 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/A isolated CHD: PAD
S0176 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/A isolated CHD: PAD
S0177 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/A isolated CHD: PAD
S0178 missense_variant MTHFD1 NM_001364837.1:c.1958G>A A/A isolated CHD: PAD
S0179 missense_variant MTHFD1 NM_001364837.1:c.1958G>A A/A isolated CHD: PAD
S0180 missense_variant MTHFD1 NM_001364837.1:c.1958G>A A/A isolated CHD: PAD
S0181 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G isolated CHD: PAD
S0182 missense_variant MTHFD1 NM_001364837.1:c.1958G>A A isolated CHD: PAD
S0207 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G and G/G(father and mother) isolated CHD: PAD
S0208 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G and G/A(or A/A)(father and mother) isolated CHD: PAD
S0209 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/A and G/A(or A/A)(father and mother) isolated CHD: PAD
S0210 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: PAD

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