All of V0064

ID Consequence Gene/Location Detail Geno Type CHD Type
S0265 missense_variant CBS NM_000071.2:c.919G>A G/G isolated CHD: ASD
S0266 missense_variant CBS NM_000071.2:c.919G>A G/A isolated CHD: ASD
S0267 missense_variant CBS NM_000071.2:c.919G>A A/A isolated CHD: ASD
S0277 missense_variant CBS NM_000071.2:c.919G>A G/G isolated CHD: ASD
S0278 missense_variant CBS NM_000071.2:c.919G>A G/A isolated CHD: ASD
S0279 missense_variant CBS NM_000071.2:c.919G>A A/A isolated CHD: ASD
S0280 missense_variant CBS NM_000071.2:c.919G>A G/G isolated CHD: ASD
S0281 missense_variant CBS NM_000071.2:c.919G>A G/A isolated CHD: ASD
S0282 missense_variant CBS NM_000071.2:c.919G>A A/A isolated CHD: ASD