Filter SNVs Using Feature Selection

Show entries
545941 SNVs 1 of 54595 Pages
Individual SNV ID Position Inidvidual Gene: Location Reference Alteration Genotype
MACSNP016036100663 chr8: 395439 SM2 ENSMMUG00000011105: Intron
G A
homozygote
MACSNP016036100673 chr8: 395585 SM2 ENSMMUG00000011105: Intron
G A
homozygote
MACSNP016036100685 chr8: 395904 SM2 ENSMMUG00000011105: Intron
A G
homozygote
MACSNP016036100698 chr8: 396171 SM2 ENSMMUG00000011105: Intron
A G
homozygote
MACSNP016036100701 chr8: 396338 SM2 ENSMMUG00000011105: Intron
G A
homozygote
MACSNP016036100703 chr8: 396371 SM2 ENSMMUG00000011105: Intron
T C
homozygote
MACSNP016036100710 chr8: 396590 SM2 ENSMMUG00000011105: Intron
T G
homozygote
MACSNP016036100723 chr8: 397000 SM2 ENSMMUG00000011105: Intron
G A
homozygote
MACSNP016036100724 chr8: 397048 SM2 ENSMMUG00000011105: Intron
T C
homozygote
MACSNP016036100732 chr8: 397231 SM2 ENSMMUG00000011105: Intron
G T
homozygote