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COSMIC Non Coding Variants VCF
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 VCF file of all non coding variants in the current release. [ Cosmic_NonCodingVariants_v103_GRCh38.vcf.gz ]

  File Description

##fileformat=VCFv4.1
##source=COSMICv103
##reference=GRCh38
##fileDate=20250903
##comment="Missing nucleotide details indicate ambiguity during curation process"
##comment="URL stub for ID field (use the whole COSV identifier)='https://cancer.sanger.ac.uk/cosmic/search?genome=38&q='"
##comment="REF and ALT sequences are both forward strand
##INFO=<ID=GENE,Number=1,Type=String,Description="Gene name">
##INFO=<ID=TRANSCRIPT,Number=1,Type=String,Description="Transcript accession">
##INFO=<ID=STRAND,Number=1,Type=String,Description="Gene strand">
##INFO=<ID=LEGACY_ID,Number=1,Type=String,Description="Legacy Mutation ID">
##INFO=<ID=HGVSG,Number=1,Type=String,Description="HGVS genomic syntax">
##INFO=<ID=SAMPLE_COUNT,Number=1,Type=Integer,Description="How many samples have this mutation">
##INFO=<ID=IS_CANONICAL,Number=1,Type=String,Description="The Ensembl Canonical transcript is a single, representative transcript identified at every locus. For details see: https://www.ensembl.org/info/genome/genebuild/canonical.html">
##INFO=<ID=TIER,Number=1,Type=String,Description="Indicates to which tier of the Cancer Gene Census the gene belongs (1/2)">
##INFO=<ID=SO_TERM,Number=1,Type=String,Description="SO term for this mutation">
#CHROM  POS     ID      REF     ALT     QUAL    FILTER  INFO
