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Filter SNVs Using Feature Selection

Chromosome chr1 chr2 chr3 chr4 chr5 chr6 chr7 chr8 chr9 chr10 chr11 chr12 chr13 chr14 chr15 chr16 chr17 chr18 chr19 chr20
Individual All CR1 CR2 CR3 TW1 JM1 JM2 CE1 CE2 CE3 CE4 CE5 TM1 TM2 AM1 SM1 SM2 PM1 PM2 LM1 BM1
Gene feature All CDS EXON 3'UTR INTRON 5'UTR Genotype All homozygote heterozygote Mutation All non-synonymous synonymous
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643439 SNVs 1 of 64344 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP016015522763 chr4: 17469 SM2 Intergenic G A
homozygote
MACSNP016015522785 chr4: 18174 SM2 Intergenic T C
homozygote
MACSNP016015522793 chr4: 18481 SM2 Intergenic A G
homozygote
MACSNP016015522796 chr4: 18548 SM2 Intergenic G T
homozygote
MACSNP016015522808 chr4: 19220 SM2 Intergenic G C
homozygote
MACSNP016015522813 chr4: 19306 SM2 Intergenic C T
heterozygote
MACSNP016015522826 chr4: 19818 SM2 Intergenic G T
homozygote
MACSNP016015522829 chr4: 19918 SM2 Intergenic T C
homozygote
MACSNP016015522831 chr4: 19952 SM2 Intergenic C T
homozygote
MACSNP016015522840 chr4: 20262 SM2 Intergenic C T
homozygote

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