Filter SNVs Using Feature Selection

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275454 SNVs 1 of 27546 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP013072229820 chr20: 4762 TM2 ENSMMUG00000000586: Intron
T C
homozygote
MACSNP013072229822 chr20: 4833 TM2 ENSMMUG00000000586: Intron
G A
homozygote
MACSNP013072229832 chr20: 5475 TM2 ENSMMUG00000000586: Intron
T C
homozygote
MACSNP013072229840 chr20: 5806 TM2 ENSMMUG00000000586: Intron
C T
homozygote
MACSNP013072229852 chr20: 7174 TM2 ENSMMUG00000000586: Intron
A C
homozygote
MACSNP013072229867 chr20: 8449 TM2 ENSMMUG00000000586: Intron
C G
homozygote
MACSNP013072229873 chr20: 8700 TM2 ENSMMUG00000000586: Intron
C G
homozygote
MACSNP013072229893 chr20: 9635 TM2 ENSMMUG00000000586: CDS
ENSMMUG00000047475: 5'UTR
C T
homozygote
MACSNP013072229908 chr20: 9999 TM2 ENSMMUG00000047475: 5'UTR
T G
homozygote
MACSNP013072229939 chr20: 11042 TM2 ENSMMUG00000047475: Intron
C T
homozygote