All of V0052

ID Consequence Gene/Location Detail Geno Type CHD Type
S0161 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G isolated CHD: VSD
S0162 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G isolated CHD: VSD
S0163 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G isolated CHD: VSD
S0164 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/A isolated CHD: VSD
S0165 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/A isolated CHD: VSD
S0166 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/A isolated CHD: VSD
S0167 missense_variant MTHFD1 NM_001364837.1:c.1958G>A A/A isolated CHD: VSD
S0168 missense_variant MTHFD1 NM_001364837.1:c.1958G>A A/A isolated CHD: VSD
S0169 missense_variant MTHFD1 NM_001364837.1:c.1958G>A A/A isolated CHD: VSD
S0170 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G isolated CHD: VSD
S0171 missense_variant MTHFD1 NM_001364837.1:c.1958G>A A isolated CHD: VSD
S0203 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G and G/G(father and mother) isolated CHD: VSD
S0204 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/G and G/A(or A/A)(father and mother) isolated CHD: VSD
S0205 missense_variant MTHFD1 NM_001364837.1:c.1958G>A G/A and G/A(or A/A)(father and mother) isolated CHD: VSD
S0206 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: VSD

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