All of V0600

ID Consequence Gene/Location Detail Geno Type CHD Type
S1424 missense_variant MTHFR NM_005957.5:c.677T>C C/C isolated CHD/non-isolated CHD: NA
S1425 missense_variant MTHFR NM_005957.5:c.677T>C C/T isolated CHD/non-isolated CHD: NA
S1426 missense_variant MTHFR NM_005957.5:c.677T>C T/T isolated CHD/non-isolated CHD: NA
S1427 missense_variant MTHFR NM_005957.5:c.677T>C C/T+T/T isolated CHD/non-isolated CHD: NA
S1440 missense_variant MTHFR NM_005957.5:c.677T>C C/C isolated CHD/non-isolated CHD: NA
S1442 missense_variant MTHFR NM_005957.5:c.677T>C C/C isolated CHD/non-isolated CHD: NA
S1443 missense_variant MTHFR NM_005957.5:c.677T>C C/T isolated CHD/non-isolated CHD: NA
S1444 missense_variant MTHFR NM_005957.5:c.677T>C C/T isolated CHD/non-isolated CHD: NA
S1445 missense_variant MTHFR NM_005957.5:c.677T>C C/T isolated CHD/non-isolated CHD: NA
S1446 missense_variant MTHFR NM_005957.5:c.677T>C T/T isolated CHD/non-isolated CHD: NA
S1447 missense_variant MTHFR NM_005957.5:c.677T>C T/T isolated CHD/non-isolated CHD: NA
S1448 missense_variant MTHFR NM_005957.5:c.677T>C T/T isolated CHD/non-isolated CHD: NA