All of V1189

ID Consequence Gene/Location Detail Geno Type CHD Type
S2493 missense_variant BMPR2 NM_001204.7:c.1042G>A A isolated CHD/non-isolated CHD: PVD
S2494 missense_variant BMPR2 NM_001204.7:c.1042G>A A isolated CHD/non-isolated CHD: PVD
S2495 missense_variant BMPR2 NM_001204.7:c.1042G>A A isolated CHD/non-isolated CHD: PVD
S2496 missense_variant BMPR2 NM_001204.7:c.1042G>A A isolated CHD/non-isolated CHD: PVD
S2497 missense_variant BMPR2 NM_001204.7:c.1042G>A A isolated CHD/non-isolated CHD: PVD
S2498 missense_variant BMPR2 NM_001204.7:c.1042G>A A isolated CHD/non-isolated CHD: PVD

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