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##fileformat=VCFv4.2
##INFO=<ID=CSQ,Number=.,Type=String,Description="Consequence annotations from Ensembl VEP. Format: Allele|Consequence|IMPACT|SYMBOL|Gene|Feature_type|Feature|BIOTYPE|EXON|INTRON|HGVSc|HGVSp|cDNA_position|CDS_position|Protein_position|Amino_acids|Codons|Existing_variation|DISTANCE|STRAND|FLAGS|VARIANT_CLASS|SYMBOL_SOURCE|HGNC_ID|CANONICAL|MANE_SELECT|MANE_PLUS_CLINICAL|TSL|APPRIS|CCDS|ENSP|SWISSPROT|TREMBL|UNIPARC|UNIPROT_ISOFORM|GENE_PHENO|SIFT|PolyPhen|DOMAINS|miRNA|HGVS_OFFSET|AF|AFR_AF|AMR_AF|EAS_AF|EUR_AF|SAS_AF|AA_AF|EA_AF|gnomAD_AF|gnomAD_AFR_AF|gnomAD_AMR_AF|gnomAD_ASJ_AF|gnomAD_EAS_AF|gnomAD_FIN_AF|gnomAD_NFE_AF|gnomAD_OTH_AF|gnomAD_SAS_AF|MAX_AF|MAX_AF_POPS|CLIN_SIG|SOMATIC|PHENO|PUBMED|MOTIF_NAME|MOTIF_POS|HIGH_INF_POS|MOTIF_SCORE_CHANGE|TRANSCRIPTION_FACTORS|ExACpLI|CADD_PHRED|CADD_RAW|M-CAP_pred|M-CAP_score|TSSDistance">
#CHROM POS ID REF ALT QUAL FILTER INFO
9 94487044 . C T . . CSQ=T|missense_variant|MODERATE|ROR2|ENSG00000169071|Transcript|ENST00000375708|protein_coding|9/9||ENST00000375708.3:c.1732G>A|ENSP00000364860.3:p.Asp578Asn|1931|1732|578|D/N|Gat/Aat|rs139802697||-1||SNV|HGNC|10257|YES|||||CCDS6691.1|ENSP00000364860|ROR2_HUMAN||UPI000013E8CA||1|tolerated(0.13)|probably_damaging(0.999)|Superfamily:SSF56112&PIRSF:PIRSF000624&Gene3D:1.10.510.10&Pfam:PF07714&PANTHER:PTHR24416:SF132&PANTHER:PTHR24416&PROSITE_profiles:PS50011|||||||||0.000227|0|3.192e-05|6.165e-05|5.789e-05|0|0|0|4.416e-05|0|0|0.000227|AA||||||||||0.46|23.5|2.953273|D|0.293271|
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