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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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471482 SNVs 1 of 47149 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP003036100636 chr8: 223246 CR3 Intergenic G A
heterozygote
MACSNP003036100647 chr8: 234126 CR3 ENSMMUG00000020598: Intron
 C A
homozygote
MACSNP003036100651 chr8: 234602 CR3 ENSMMUG00000020598: Intron
 G C
heterozygote
MACSNP003036100698 chr8: 396171 CR3 ENSMMUG00000011105: Intron
 A G
homozygote
MACSNP003036100703 chr8: 396371 CR3 ENSMMUG00000011105: Intron
 T C
homozygote
MACSNP003036100709 chr8: 396579 CR3 ENSMMUG00000011105: Intron
 G A
homozygote
MACSNP003036100710 chr8: 396590 CR3 ENSMMUG00000011105: Intron
 T G
homozygote
MACSNP003036100737 chr8: 397398 CR3 ENSMMUG00000011105: Intron
 T G
heterozygote
MACSNP003036100739 chr8: 397453 CR3 ENSMMUG00000011105: Intron
 A G
heterozygote
MACSNP003036100745 chr8: 397575 CR3 ENSMMUG00000011105: Intron
 A C
heterozygote

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