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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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505564 SNVs 1 of 50557 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP013036100639 chr8: 232232 TM2 ENSMMUG00000020598: Intron
 A G
heterozygote
MACSNP013036100663 chr8: 395439 TM2 ENSMMUG00000011105: Intron
 G A
homozygote
MACSNP013036100672 chr8: 395584 TM2 ENSMMUG00000011105: Intron
 C T
homozygote
MACSNP013036100685 chr8: 395904 TM2 ENSMMUG00000011105: Intron
 A G
homozygote
MACSNP013036100695 chr8: 396150 TM2 ENSMMUG00000011105: Intron
 G C
homozygote
MACSNP013036100698 chr8: 396171 TM2 ENSMMUG00000011105: Intron
 A G
homozygote
MACSNP013036100701 chr8: 396338 TM2 ENSMMUG00000011105: Intron
 G A
homozygote
MACSNP013036100703 chr8: 396371 TM2 ENSMMUG00000011105: Intron
 T C
homozygote
MACSNP013036100710 chr8: 396590 TM2 ENSMMUG00000011105: Intron
 T G
homozygote
MACSNP013036100723 chr8: 397000 TM2 ENSMMUG00000011105: Intron
 G A
homozygote

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