All of V0066

ID Consequence Gene/Location Detail Geno Type CHD Type
S0271 missense_variant CBS NM_000071.2:c.919G>A G/G isolated CHD: PDA
S0272 missense_variant CBS NM_000071.2:c.919G>A G/A isolated CHD: PDA
S0273 missense_variant CBS NM_000071.2:c.919G>A A/A isolated CHD: PDA
S0289 missense_variant CBS NM_000071.2:c.919G>A G/G isolated CHD: PDA
S0290 missense_variant CBS NM_000071.2:c.919G>A G/A isolated CHD: PDA
S0291 missense_variant CBS NM_000071.2:c.919G>A A/A isolated CHD: PDA
S0292 missense_variant CBS NM_000071.2:c.919G>A G/G isolated CHD: PDA
S0293 missense_variant CBS NM_000071.2:c.919G>A G/A isolated CHD: PDA
S0294 missense_variant CBS NM_000071.2:c.919G>A A/A isolated CHD: PDA

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