EGFR_mutations_indelfindr_demo.validation_check.vcf

##fileformat=VCFv4.3
##filedate= 2022-04-01 
##source="Produced with write.vcf() of indelfindR R package v0.0.1 for complex indel detection"
##INFO=<ID=AF,Number=A,Type=Float,Description="Allele Frequency">
##INFO=<ID=SB,Number=A,Type=Float,Description="Strand Bias Pvalue">
##INFO=<ID=RF,Number=A,Type=Float,Description="Reference Forward Count">
##INFO=<ID=RR,Number=A,Type=Float,Description="Reference Reverse Count">
##INFO=<ID=VF,Number=A,Type=Float,Description="Alternate Forward Count">
##INFO=<ID=VR,Number=A,Type=Float,Description="Alternate Reverse Count">
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Read Depth">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO	FORMAT	EGFR_mutation_bam 
chr7	55174772	.	GGAATTAAGAGAAGCA	G	.	.	AF=0.95;SB=0.45;RF=1;RR=0;VF=8;VR=11	GT:DP	./.:20
chr7	55181316	.	G	GGAC	.	.	AF=0.116279069767442;SB=0.350808956594549;RF=19;RR=19;VF=4;VR=1	GT:DP	./.:43
chr7	55181316	.	G	GATGGCCAGCGTGGAC	.	.	AF=0.613636363636364;SB=0.54774346986151;RF=10;RR=7;VF=13;VR=14	GT:DP	./.:44