Table 6.
Position relative to gap | Variant | Transcript to genome projection |
---|---|---|
within | NM_007121.5:n.796A>T | NC_000019.10:g.50378563_50378564insTAC |
NM_007121.5:n.796_797del | NC_000019.10:g.50378563_50378564insC | |
NM_007121.5:n.796_797insT | NC_000019.10:g.50378564_50378565insTACA | |
exact | NM_007121.5:n.796_798del | NC_000019.10:g.50378 565_50378567dup |
NM_007121.5:n.796_798delinsTC GG | NC_000019.10:g.50378563_50378564insTCGG | |
partial | NM_007121.5:n.795_796del | NC_000019.10:g.50378563_50378564insC |
NM_007121.5:n.795_796delinsTT | NC_000019.10:g.50378563delinsTTAC | |
NM_007121.5:n.795_796insT | NC_000019.10:g.50378563_50378564insTAAC | |
span | NM_007121.5:n.794_800del | NC_000019.10:g.50378562_50378565del |
NM_007121.5:n.794_800delinsTC | NC_000019.10:g.50378562_50378565delinsTC |
Position relative to gap | Variant | Transcript to genome projection |
---|---|---|
within | NM_198455.2:n.1115_1116insT | NC_000007.14:g.149779575_149779577delinsT |
exact | NM_198455.2:n.1115_1116insCAG | |
N M_198455.2:n.1115_1116= | NC_0 00007.14:g.149779576_149779578del | |
partial | NM_198455.2:n.1115_1116insCA | NC_000007.14:g.149779577del |
span | NM_198455.2:n.1114_1117del | NC_000007.14:g.149779573_149779579del |
NM_198455.2:n.1114_1117delinsCA | NC_000007.14:g.149779573_149779579delinsCA |