618 results for depdc7

(mRatBN7.2)3:91114336G>A

(Rattus norvegicus)
Allele/Variant
Source: rs197798132
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91114336G>A

(mRatBN7.2)3:91115640G>A

(Rattus norvegicus)
Allele/Variant
Source: rs197949621
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91115640G>A

(mRatBN7.2)3:91100299A>C

(Rattus norvegicus)
Allele/Variant
Source: rs199406521
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91100299A>C

(mRatBN7.2)3:91109160G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319936134
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91109160G>T

(mRatBN7.2)3:91110792T>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051338.1:g.91110792T>A
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91110792T>A

(mRatBN7.2)3:91100331C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051338.1:g.91100331C>T
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91100331C>T

(mRatBN7.2)3:91109168G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319984021
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91109168G>T

(mRatBN7.2)3:91100759A>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051338.1:g.91100759A>T
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91100759A>T

(mRatBN7.2)3:91100667G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319936132
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91100667G>A

(mRatBN7.2)3:91113362C>T

(Rattus norvegicus)
Allele/Variant
Source: rs198735132
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91113362C>T

(mRatBN7.2)3:91116406G>A

(Rattus norvegicus)
Allele/Variant
Source: rs199200288
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91116406G>A

(mRatBN7.2)3:91116571G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198649490
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91116571G>A

(mRatBN7.2)3:91116591A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051338.1:g.91116591A>G
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91116591A>G

rs198006217

(Rattus norvegicus)
Allele/Variant
Source: rs198006217
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available

(mRatBN7.2)3:91106406C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197654364
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91106406C>T

(mRatBN7.2)3:91106898C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319972517
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91106898C>T

(mRatBN7.2)3:91107638C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197108333
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91107638C>T

(mRatBN7.2)3:91109164G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319936024
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91109164G>T

(mRatBN7.2)3:91114334A>C

(Rattus norvegicus)
Allele/Variant
Source: rs198442452
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91114334A>C

(mRatBN7.2)3:91111897A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319965675
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91111897A>T

(mRatBN7.2)3:91101879C>G

(Rattus norvegicus)
Allele/Variant
Source: rs198596458
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91101879C>G

(mRatBN7.2)3:91111551C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051338.1:g.91111551C>T
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91111551C>T

(mRatBN7.2)3:91114293G>T

(Rattus norvegicus)
Allele/Variant
Source: rs199345478
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91114293G>T

(mRatBN7.2)3:91100758G>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051338.1:g.91100758G>C
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91100758G>C

(mRatBN7.2)3:91100765A>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051338.1:g.91100765A>T
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91100765A>T

(mRatBN7.2)3:91103867A>G

(Rattus norvegicus)
Allele/Variant
Source: rs197425698
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91103867A>G

(mRatBN7.2)3:91100510C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319974713
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91100510C>T

Allele/Variant
Source: rs27414479
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104552290T>C

Allele/Variant
Source: rs213732276
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104552757C>A

Allele/Variant
Source: rs579266903
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104552767T>C

Allele/Variant
Source: rs27414471
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104555045A>G

Allele/Variant
Source: rs259365421
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104555084G>A

Allele/Variant
Source: rs259283757
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104555714G>A

Allele/Variant
Source: rs239090841
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104556617C>A

Allele/Variant
Source: rs265353967
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104556634A>G

Allele/Variant
Source: rs220364923
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104557272T>C

Allele/Variant
Source: rs239617694
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104557549G>A

Allele/Variant
Source: rs256832726
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104557671G>C

Allele/Variant
Source: rs585805131
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104558348T>C

Allele/Variant
Source: rs1134675920
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104558826G>T

Allele/Variant
Source: rs229086582
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104559013G>A

Allele/Variant
Source: rs265375929
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104560081C>T

Allele/Variant
Source: rs222127935
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104561082A>T

Allele/Variant
Source: rs33154284
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104561643T>G

Allele/Variant
Source: rs246063620
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104562032G>A

Allele/Variant
Source: rs260773215
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104562691C>T

Allele/Variant
Source: rs242846363
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104563326C>T

Allele/Variant
Source: rs220658621
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104566757G>A

Allele/Variant
Source: rs224063386
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104567170G>A

Allele/Variant
Source: rs583667654
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:104564600C>T