All of V0938

ID Consequence Gene/Location Detail Geno Type CHD Type
S2052 5_prime_UTR_variant RCAN1 NC_000021.9:g.34615054G>A G/G isolated CHD : ASD/VSD/TOF/PDA/CoA/other
S2053 5_prime_UTR_variant RCAN1 NC_000021.9:g.34615054G>A G/A isolated CHD : ASD/VSD/TOF/PDA/CoA/other
S2054 5_prime_UTR_variant RCAN1 NC_000021.9:g.34615054G>A A/A isolated CHD : ASD/VSD/TOF/PDA/CoA/other
S2055 5_prime_UTR_variant RCAN1 NC_000021.9:g.34615054G>A G/A+A/A isolated CHD : ASD/VSD/TOF/PDA/CoA/other
S2056 5_prime_UTR_variant RCAN1 NC_000021.9:g.34615054G>A G/G isolated CHD : ASD/VSD/TOF/PDA/CoA/other
S2057 5_prime_UTR_variant RCAN1 NC_000021.9:g.34615054G>A G/A isolated CHD : ASD/VSD/TOF/PDA/CoA/other
S2058 5_prime_UTR_variant RCAN1 NC_000021.9:g.34615054G>A A/A isolated CHD : ASD/VSD/TOF/PDA/CoA/other
S2059 5_prime_UTR_variant RCAN1 NC_000021.9:g.34615054G>A G/A+A/A isolated CHD : ASD/VSD/TOF/PDA/CoA/other
S2060 5_prime_UTR_variant RCAN1 NC_000021.9:g.34615054G>A G/G isolated CHD : ASD/VSD/TOF/PDA/CoA/other
S2061 5_prime_UTR_variant RCAN1 NC_000021.9:g.34615054G>A G/A isolated CHD : ASD/VSD/TOF/PDA/CoA/other
S2062 5_prime_UTR_variant RCAN1 NC_000021.9:g.34615054G>A A/A isolated CHD : ASD/VSD/TOF/PDA/CoA/other
S2063 5_prime_UTR_variant RCAN1 NC_000021.9:g.34615054G>A G/A+A/A isolated CHD : ASD/VSD/TOF/PDA/CoA/other

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