356 results
Allele/Variant Genes: nox1 (Dre)
Allele/Variant
Source: ss5198457714
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41345942C>T

Allele/Variant
Source: ss5198457750
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41346033A>T

Allele/Variant
Source: ss5198457747
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41346169T>G

Allele/Variant
Source: ss5198457741
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41346279C>T

Allele/Variant
Source: ss5198457847
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41347013T>A

Allele/Variant
Source: ss5198457869
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41347041C>T

Allele/Variant
Source: ss5198458054
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41356728T>C

Allele/Variant
Source: ss5198457910
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41348638T>G

Allele/Variant
Source: ss5198457902
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41349912T>A

Allele/Variant
Source: ss5198458043
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41357819A>C

Allele/Variant
Source: ss5198457745
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41346436A>T

Allele/Variant
Source: ss5198457826
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41346661G>A

Allele/Variant
Source: ss5198458148
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41358197G>A

Allele/Variant
Source: ss5198458180
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41358214T>C

Allele/Variant
Source: ss5198458101
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41360834A>G

Allele/Variant
Source: ss5198457942
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41349098T>A

Allele/Variant
Source: ss5198457964
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41349188T>A

Allele/Variant
Source: ss5198457948
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41349590A>C

Allele/Variant
Source: ss5198457961
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41350924G>T

Allele/Variant
Source: ss5198458037
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41354221G>A

Allele/Variant
Source: ss5198457788
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41345760A>G

Allele/Variant
Source: ss5198457753
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41345795A>T

Allele/Variant
Source: ss5198458067
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41355893G>A

Allele/Variant
Source: ss5198458004
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41356699C>T

Allele/Variant
Source: ss5198458090
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41356921G>A

Allele/Variant
Source: ss5198458093
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41357465C>T

Allele/Variant
Source: ss5198458062
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41357803T>C

Allele/Variant
Source: ss5198458188
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41358084T>C

Allele/Variant
Source: ss5198458169
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41360947A>T

Allele/Variant
Source: ss5198458159
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41361307A>T

Allele/Variant
Source: ss5198457786
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41345730T>C

Allele/Variant
Source: ss5198457735
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41345937T>A

Allele/Variant
Source: ss5198457742
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41345972A>T

Allele/Variant
Source: ss5198457890
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41347248G>A

Allele/Variant
Source: ss5198458011
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41356002A>G

Allele/Variant
Source: ss5198458091
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41356804T>C

Allele/Variant
Source: ss5198458012
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41357193T>A

Allele/Variant
Source: ss5198457892
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41348390T>G

Allele/Variant
Source: ss5198457887
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41347340A>T

Allele/Variant
Source: ss5198457800
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41347446A>G

Allele/Variant
Source: ss5198458024
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41354416A>C

Allele/Variant
Source: ss5198458058
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41357858T>C

Allele/Variant
Source: ss5198458046
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41357963A>C

Allele/Variant
Source: ss5198458051
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41354607T>C

Allele/Variant
Source: ss5198458059
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41358036A>G

Allele/Variant
Source: ss5198458015
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41355517A>C

Allele/Variant
Source: ss5198458071
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41356004A>G

Allele/Variant
Source: ss5198458086
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41356145G>A

Allele/Variant
Source: ss5198458075
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41357207A>G

Allele/Variant
Source: ss5198458036
Genes: nox1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)14:41357726A>G