All of V0065

ID Consequence Gene/Location Detail Geno Type CHD Type
S0268 missense_variant CBS NM_000071.2:c.919G>A G/G isolated CHD: VSD
S0269 missense_variant CBS NM_000071.2:c.919G>A G/A isolated CHD: VSD
S0270 missense_variant CBS NM_000071.2:c.919G>A A/A isolated CHD: VSD
S0283 missense_variant CBS NM_000071.2:c.919G>A G/G isolated CHD: VSD
S0284 missense_variant CBS NM_000071.2:c.919G>A G/A isolated CHD: VSD
S0285 missense_variant CBS NM_000071.2:c.919G>A A/A isolated CHD: VSD
S0286 missense_variant CBS NM_000071.2:c.919G>A G/G isolated CHD: VSD
S0287 missense_variant CBS NM_000071.2:c.919G>A G/A isolated CHD: VSD
S0288 missense_variant CBS NM_000071.2:c.919G>A A/A isolated CHD: VSD

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