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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
Show entries
219925 SNVs 1 of 21993 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP004072229841 chr20: 5846 TW1 ENSMMUG00000000586: Intron
 G A
homozygote
MACSNP004072229843 chr20: 5977 TW1 ENSMMUG00000000586: Intron
 G A
homozygote
MACSNP004072229845 chr20: 6063 TW1 ENSMMUG00000000586: Intron
 A T
homozygote
MACSNP004072229850 chr20: 7004 TW1 ENSMMUG00000000586: Intron
 T G
homozygote
MACSNP004072229854 chr20: 7258 TW1 ENSMMUG00000000586: Intron
 T C
homozygote
MACSNP004072229883 chr20: 9115 TW1 ENSMMUG00000000586: Intron
 A G
homozygote
MACSNP004072229901 chr20: 9906 TW1 ENSMMUG00000047475: 5'UTR
 G A
homozygote
MACSNP004072229915 chr20: 10349 TW1 ENSMMUG00000047475: Intron
 A C
homozygote
MACSNP004072229918 chr20: 10450 TW1 ENSMMUG00000047475: Intron
 C A
homozygote
MACSNP004072229920 chr20: 10514 TW1 ENSMMUG00000047475: Intron
 A G
homozygote

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