I am calculating allelic frequency for somatic variants. VEP gives a VCF file, for example that has:
9761707 G>A and outputs
DP FDP SDP SUBDP AU CU GU TU
99 0 0 0 0,0 0,0 99,99 0,0
or
121467604 T > C
DP FDP SDP SUBDP AU CU GU TU
153 0 0 0 0,0 77,79 0,0 76,76
How can I calculate the allele frequency from this information? I don't quite understand why in the first case there is nothing on AU, but the second case has something on both CU and TU. Based on my readings (recommendation here) it should be:
AU1/(AU1+GU1) for the first one and CU1/(CU1+TU1) for the second one. Yet, on the first case this would mean an allelic frequency of zero, but then why is the variant being reported at all??
Why is this?