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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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335089 SNVs 1 of 33509 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP003050510057 chr12: 38443 CR3 ENSMMUG00000009617: Intron
 C G
homozygote
MACSNP003050510067 chr12: 39590 CR3 Intergenic G A
homozygote
MACSNP003050510070 chr12: 40345 CR3 Intergenic G A
heterozygote
MACSNP003050510072 chr12: 40601 CR3 Intergenic T C
heterozygote
MACSNP003050510074 chr12: 40777 CR3 Intergenic C T
homozygote
MACSNP003050510088 chr12: 47142 CR3 Intergenic C A
homozygote
MACSNP003050510089 chr12: 47162 CR3 Intergenic G T
homozygote
MACSNP003050510094 chr12: 47511 CR3 Intergenic C T
heterozygote
MACSNP003050510095 chr12: 47633 CR3 Intergenic C A
heterozygote
MACSNP003050510097 chr12: 47701 CR3 Intergenic C T
heterozygote

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