Version: 8.0.0
Date: Tue Jan 28 2025
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Gene
Gene Ontology
Disease
Allele/Variant
Model
HTP Dataset Index
Category
Allele/Variant
606
Gene
8
Gene Ontology
4
Filter
618
results
for
depdc7
Page 2 of 13
(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
(GRCm39)2:104552290T>C
(
Mus musculus
)
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
(GRCm39)2:104552757C>A
(
Mus musculus
)
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
(GRCm39)2:104552767T>C
(
Mus musculus
)
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
(GRCm39)2:104555045A>G
(
Mus musculus
)
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
(GRCm39)2:104555084G>A
(
Mus musculus
)
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
(GRCm39)2:104555714G>A
(
Mus musculus
)
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
(GRCm39)2:104556617C>A
(
Mus musculus
)
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
(GRCm39)2:104556634A>G
(
Mus musculus
)
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
(GRCm39)2:104557272T>C
(
Mus musculus
)
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
(GRCm39)2:104557549G>A
(
Mus musculus
)
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
(GRCm39)2:104557671G>C
(
Mus musculus
)
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
(GRCm39)2:104558348T>C
(
Mus musculus
)
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
(GRCm39)2:104558826G>T
(
Mus musculus
)
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
(GRCm39)2:104559013G>A
(
Mus musculus
)
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
(GRCm39)2:104560081C>T
(
Mus musculus
)
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
(GRCm39)2:104561082A>T
(
Mus musculus
)
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
(GRCm39)2:104561643T>G
(
Mus musculus
)
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
(GRCm39)2:104562032G>A
(
Mus musculus
)
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
(GRCm39)2:104562691C>T
(
Mus musculus
)
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
(GRCm39)2:104563326C>T
(
Mus musculus
)
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
(GRCm39)2:104566757G>A
(
Mus musculus
)
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
(GRCm39)2:104567170G>A
(
Mus musculus
)
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
(GRCm39)2:104564600C>T
(
Mus musculus
)
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
Page 2 of 13
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