Hello everyone,
I have a VCF file and I got a little confused. I just need a small clarification.
#CHROM  POS ID  REF ALT QUAL    FILTER  INFO    FORMAT  Control Subject
10  15936159    .   C   T,<*>   0   .   DP=123;ADF=54,9,0;ADR=52,8,0;AD=106,17,0;SCR=64;I16=54,52,9,8,3980,243762,675,52205,1714,69200,412,16468,2281,54527,423,10529;QS=1.78256,0.217441,0;VDB=0.0414177;SGB=-7.17793;RPB=0.011324;MQB=0.0522971;MQSB=0.278527;BQB=0.987088;MQ0F=0.520325  PL:DP:SP:ADF:ADR:AD:SCR:QS  0,48,255,66,255,255:24:0:15,1,0:7,1,0:22,2,0:3:724,8,0  0,22,145,253,190,248:99:1:39,8,0:45,7,0:84,15,0:61:926,241,0
- Kindly please confirm whether my below-mentioned assumptions are valid considering the above information from the VCF file. - Total number of reads at this position is 123 (Control 24 reads and Subject 99 reads).
- For 'Control' out of 24 reads, 22 reads assigned for the reference allele (C) and 2 reads assigned to alternate allele (T).
- For 'Subject' out of 99 reads, 84 reads assigned for the reference allele (C) and 15 reads assigned to alternate allele (T).
 
- Also, one more question. Is there any easy way to add proportion/fraction/percentage of reads assigned to reference and alternate alleles for 'Control' and 'Subject' per SNP? or do I have to create a custom script for that? 
Update: I found a solution for question 2 using bcftools. Here it is.
bcftools plugin fill-tags myVCF.vcf -- -t "FORMAT/VAF" > myVCF_allele_proportion.vcf
Thank you.
Can you please share what is the version of given file, and maybe the full file. Have you read VCF version xx manual?