All of V0068

ID Consequence Gene/Location Detail Geno Type CHD Type
S0301 missense_variant CBS NM_000071.2:c.919G>A G/G isolated CHD: NA
S0302 missense_variant CBS NM_000071.2:c.919G>A G/A isolated CHD: NA
S0303 missense_variant CBS NM_000071.2:c.919G>A A/A isolated CHD: NA
S0304 missense_variant CBS NM_000071.2:c.919G>A G isolated CHD: NA
S0305 missense_variant CBS NM_000071.2:c.919G>A A isolated CHD: NA
S0306 missense_variant CBS NM_000071.2:c.919G>A G/G isolated CHD: NA
S0307 missense_variant CBS NM_000071.2:c.919G>A G/A isolated CHD: NA
S0308 missense_variant CBS NM_000071.2:c.919G>A A/A isolated CHD: NA
S0309 missense_variant CBS NM_000071.2:c.919G>A G isolated CHD: NA
S0310 missense_variant CBS NM_000071.2:c.919G>A A isolated CHD: NA
S0311 missense_variant CBS NM_000071.2:c.919G>A G/G isolated CHD: NA
S0312 missense_variant CBS NM_000071.2:c.919G>A G/A isolated CHD: NA
S0313 missense_variant CBS NM_000071.2:c.919G>A A/A isolated CHD: NA
S0314 missense_variant CBS NM_000071.2:c.919G>A G isolated CHD: NA
S0315 missense_variant CBS NM_000071.2:c.919G>A A isolated CHD: NA
S0316 missense_variant CBS NM_000071.2:c.919G>A G/G isolated CHD: NA
S0317 missense_variant CBS NM_000071.2:c.919G>A G/A isolated CHD: NA
S0318 missense_variant CBS NM_000071.2:c.919G>A A/A isolated CHD: NA
S0319 missense_variant CBS NM_000071.2:c.919G>A G/G isolated CHD: NA
S0320 missense_variant CBS NM_000071.2:c.919G>A G/A isolated CHD: NA
S0321 missense_variant CBS NM_000071.2:c.919G>A A/A isolated CHD: NA
S0322 missense_variant CBS NM_000071.2:c.919G>A G/G isolated CHD: NA
S0323 missense_variant CBS NM_000071.2:c.919G>A G/A isolated CHD: NA
S0324 missense_variant CBS NM_000071.2:c.919G>A A/A isolated CHD: NA

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