All of V0051

ID Consequence Gene/Location Detail Geno Type CHD Type
S0150 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G isolated CHD: ASD
S0151 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G isolated CHD: ASD
S0152 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G isolated CHD: ASD
S0153 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/A isolated CHD: ASD
S0154 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/A isolated CHD: ASD
S0155 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/A isolated CHD: ASD
S0156 missense_variant MTHFD1 NM_001364837.1:c.1958G>A A/A isolated CHD: ASD
S0157 missense_variant MTHFD1 NM_001364837.1:c.1958G>A A/A isolated CHD: ASD
S0158 missense_variant MTHFD1 NM_001364837.1:c.1958G>A A/A isolated CHD: ASD
S0159 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G isolated CHD: ASD
S0160 missense_variant MTHFD1 NM_001364837.1:c.1958G>A A isolated CHD: ASD
S0199 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G and G/G(father and mother) isolated CHD: ASD
S0200 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G and G/A(or A/A)(father and mother) isolated CHD: ASD
S0201 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/A and G/A(or A/A)(father and mother) isolated CHD: ASD
S0202 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: ASD

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