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11 47368967 47368979 MYBPC3
11 47368970 47369035 MYBPC3
11 47369196 47369236 MYBPC3
This file has been truncated, but you can view the full file.
##fileformat=VCFv4.0
##FILTER=<ID=PASS,Description="All filters passed">
##fileDate=20170403
##source=dbSNP
##dbSNP_BUILD_ID=150
##reference=GRCh37.p13
##phasing=partial
##variationPropertyDocumentationUrl=ftp://ftp.ncbi.nlm.nih.gov/snp/specs/dbSNP_BitField_latest.pdf
##INFO=<ID=RS,Number=1,Type=Integer,Description="dbSNP ID (i.e. rs number)">
##INFO=<ID=RSPOS,Number=1,Type=Integer,Description="Chr position reported in dbSNP">
This file has been truncated, but you can view the full file.
##fileformat=VCFv4.2
##FILTER=<ID=PASS,Description="All filters passed">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FILTER=<ID=RF,Description="Failed random forests filters (SNV cutoff 0.1, indels cutoff 0.2)">
##FILTER=<ID=AC0,Description="Allele Count is zero (i.e. no high-confidence genotype (GQ >= 20, DP >= 10, AB => 0.2 for het calls))">
##FILTER=<ID=InbreedingCoeff,Description="InbreedingCoeff < -0.3">
##FILTER=<ID=LCR,Description="In a low complexity region">
##FILTER=<ID=SEGDUP,Description="In a segmental duplication region">
##INFO=<ID=AC,Number=A,Type=Integer,Description="Allele count in genotypes, for each ALT allele, in the same order as listed">
##INFO=<ID=AF,Number=A,Type=Float,Description="Allele Frequency among genotypes, for each ALT allele, in the same order as listed">
##fileformat=VCFv4.2
##FILTER=<ID=PASS,Description="All filters passed">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FILTER=<ID=RF,Description="Failed random forests filters (SNV cutoff 0.1, indels cutoff 0.2)">
##FILTER=<ID=AC0,Description="Allele Count is zero (i.e. no high-confidence genotype (GQ >= 20, DP >= 10, AB => 0.2 for het calls))">
##FILTER=<ID=InbreedingCoeff,Description="InbreedingCoeff < -0.3">
##FILTER=<ID=LCR,Description="In a low complexity region">
##FILTER=<ID=SEGDUP,Description="In a segmental duplication region">
##INFO=<ID=AF,Number=A,Type=Float,Description="Allele Frequency among genotypes, for each ALT allele, in the same order as listed">
##INFO=<ID=AF_POPMAX,Number=A,Type=Float,Description="Maximum Allele Frequency across populations (excluding OTH)">
# The following table is formatted as tab separated values.
#GeneName GeneId TranscriptId BioType variants_impact_HIGH variants_impact_MODERATE variants_impact_MODIFIER variants_effect_downstream_gene_variant variants_effect_missense_variant variants_effect_structural_interaction_variant variants_effect_upstream_gene_variant
CRYAB ENSG00000109846 ENST00000227251 protein_coding 14 1 0 0 1 14 0
CRYAB ENSG00000109846 ENST00000524660 protein_coding 0 0 1 0 0 0 1
CRYAB ENSG00000109846 ENST00000525823 protein_coding 0 1 0 0 1 0 0
CRYAB ENSG00000109846 ENST00000526167 protein_coding 0 1 0 0 1 0 0
CRYAB ENSG00000109846 ENST00000526180 protein_coding 14 1 0 0 1 14 0
CRYAB ENSG00000109846 ENST00000527899 protein_coding 0 1 0 0 1 0 0
CRYAB ENSG00000109846 ENST00000527950 protein_coding 14 1 0 0 1 14 0
CRYAB ENSG00000109846 ENST00000528628 protein_coding 0 1 0 0 1 0 0
##fileformat=VCFv4.2
##FILTER=<ID=PASS,Description="All filters passed">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FILTER=<ID=RF,Description="Failed random forests filters (SNV cutoff 0.1, indels cutoff 0.2)">
##FILTER=<ID=AC0,Description="Allele Count is zero (i.e. no high-confidence genotype (GQ >= 20, DP >= 10, AB => 0.2 for het calls))">
##FILTER=<ID=InbreedingCoeff,Description="InbreedingCoeff < -0.3">
##FILTER=<ID=LCR,Description="In a low complexity region">
##FILTER=<ID=SEGDUP,Description="In a segmental duplication region">
##INFO=<ID=AF,Number=A,Type=Float,Description="Allele Frequency among genotypes, for each ALT allele, in the same order as listed">
##INFO=<ID=AF_POPMAX,Number=A,Type=Float,Description="Maximum Allele Frequency across populations (excluding OTH)">
##fileformat=VCFv4.2
##FILTER=<ID=PASS,Description="All filters passed">
##ALT=<ID=NON_REF,Description="Represents any possible alternative allele at this location">
##FILTER=<ID=LowQual,Description="Low quality">
##FORMAT=<ID=AD,Number=R,Type=Integer,Description="Allelic depths for the ref and alt alleles in the order listed">
##FORMAT=<ID=DP,Number=1,Type=Integer,Description="Approximate read depth (reads with MQ=255 or with bad mates are filtered)">
##FORMAT=<ID=GQ,Number=1,Type=Integer,Description="Genotype Quality">
##FORMAT=<ID=GT,Number=1,Type=String,Description="Genotype">
##FORMAT=<ID=MIN_DP,Number=1,Type=Integer,Description="Minimum DP observed within the GVCF block">
##FORMAT=<ID=PGT,Number=1,Type=String,Description="Physical phasing haplotype information, describing how the alternate alleles are phased in relation to one another">
[1] "trying URL 'http://probability.ca/cran/src/contrib/openssl_0.9.4.tar.gz'"
[2] "Content type 'application/x-gzip' length 1165388 bytes (1.1 Mb)"
[3] "opened URL"
[4] "=================================================="
The downloaded source packages are in
‘/state/partition2/local-scratch/dwaggott/9229044/Rtmp6egFtD/downloaded_packages’
;sldkfas;d