All of V0067

ID Consequence Gene/Location Detail Geno Type CHD Type
S0274 missense_variant CBS NM_000071.2:c.919G>A G/G isolated CHD: TOF/other
S0275 missense_variant CBS NM_000071.2:c.919G>A G/A isolated CHD: TOF/other
S0276 missense_variant CBS NM_000071.2:c.919G>A A/A isolated CHD: TOF/other
S0295 missense_variant CBS NM_000071.2:c.919G>A G/G isolated CHD: TOF/other
S0296 missense_variant CBS NM_000071.2:c.919G>A G/A isolated CHD: TOF/other
S0297 missense_variant CBS NM_000071.2:c.919G>A A/A isolated CHD: TOF/other
S0298 missense_variant CBS NM_000071.2:c.919G>A G/G isolated CHD: TOF/other
S0299 missense_variant CBS NM_000071.2:c.919G>A G/A isolated CHD: TOF/other
S0300 missense_variant CBS NM_000071.2:c.919G>A A/A isolated CHD: TOF/other

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