##fileformat=VCFv4.2
##source=ensembl;version=116;url=https://e116.ensembl.org/homo_sapiens
##INFO=<ID=VE,Number=.,Type=String,Description="Variant effect of a variant overlapping a sequence feature as computed by the ensembl variant effect pipeline. Format=Consequence|Index|Feature_type|Feature_id. Index indentifies for which variant sequence the effect is described for.">
##INFO=<ID=CSQ,Number=.,Type=String,Description="Consequence annotations from Ensembl's Variant Effect Pipeline. Format=Allele|Consequence|Feature_type|Feature|Amino_acids|SIFT">
#CHROM	POS	ID	REF	ALT	QUAL	FILTER	INFO
22	15528196	rs1312204123	A	G	.	.	VE=missense_variant|0|mRNA|ENST00000643195,non_coding_transcript_variant|0|ncRNA|ENST00000775238,intron_variant|0|primary_transcript|ENST00000775238;CSQ=G|intron_variant|primary_transcript|ENST00000775238||,G|missense_variant|mRNA|ENST00000643195|N/S|deleterious_-_low_confidence(0.05)
22	15528198	rs1985999326	G	A,T	.	.	VE=missense_variant|0|mRNA|ENST00000643195,missense_variant|1|mRNA|ENST00000643195,non_coding_transcript_variant|0|ncRNA|ENST00000775238,intron_variant|0|primary_transcript|ENST00000775238,non_coding_transcript_variant|1|ncRNA|ENST00000775238,intron_variant|1|primary_transcript|ENST00000775238;CSQ=A|missense_variant|mRNA|ENST00000643195|V/I|tolerated_-_low_confidence(1),A|intron_variant|primary_transcript|ENST00000775238||,T|intron_variant|primary_transcript|ENST00000775238||,T|missense_variant|mRNA|ENST00000643195|V/F|tolerated_-_low_confidence(0.16)
