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Date: Tue Jan 28 2025
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All
All
Gene
Gene Ontology
Disease
Allele/Variant
Model
HTP Dataset Index
Allele/Variant
Show all Categories
Species
Rattus norvegicus
34
×
Category
variant
34
×
Variant Type
SNP
34
×
Molecular Consequence
intron variant
26
×
3 prime UTR variant
4
×
missense variant
2
×
synonymous variant
2
×
Genes
Slc3a2 (Rno)
34
×
Filter
34
results
Page 1 of 1
Allele/Variant
Genes: Slc3a2 (Rno)
(mRatBN7.2)1:205614981G>A
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319168484
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205614981G>A
(mRatBN7.2)1:205616616A>G
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3323744664
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205616616A>G
(mRatBN7.2)1:205609479C>T
(
Rattus norvegicus
)
Allele/Variant
Source:
rs8155031
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
missense_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205609479C>T
(mRatBN7.2)1:205611553T>A
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3323683140
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205611553T>A
(mRatBN7.2)1:205604473G>T
(
Rattus norvegicus
)
Allele/Variant
Source:
rs8146637
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
3_prime_UTR_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205604473G>T
(mRatBN7.2)1:205617668G>A
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319178659
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205617668G>A
(mRatBN7.2)1:205608100A>C
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319161331
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205608100A>C
(mRatBN7.2)1:205608381A>G
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319178606
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205608381A>G
(mRatBN7.2)1:205614820C>G
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319144554
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205614820C>G
(mRatBN7.2)1:205616740C>T
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319181933
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205616740C>T
(mRatBN7.2)1:205604474C>A
(
Rattus norvegicus
)
Allele/Variant
Source:
rs8148884
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
3_prime_UTR_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205604474C>A
(mRatBN7.2)1:205610084G>A
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051336.1:g.205610084G>A
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
missense_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205610084G>A
(mRatBN7.2)1:205610962T>C
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319144374
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205610962T>C
(mRatBN7.2)1:205618606T>G
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319177481
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205618606T>G
(mRatBN7.2)1:205606588A>C
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319161332
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
synonymous_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205606588A>C
(mRatBN7.2)1:205616518G>A
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051336.1:g.205616518G>A
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205616518G>A
(mRatBN7.2)1:205610943T>A
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319182393
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205610943T>A
(mRatBN7.2)1:205604468A>T
(
Rattus norvegicus
)
Allele/Variant
Source:
rs8145067
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
3_prime_UTR_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205604468A>T
(mRatBN7.2)1:205604472G>T
(
Rattus norvegicus
)
Allele/Variant
Source:
rs8151382
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
3_prime_UTR_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205604472G>T
(mRatBN7.2)1:205610661G>T
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319183115
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205610661G>T
(mRatBN7.2)1:205616848A>G
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319185532
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205616848A>G
(mRatBN7.2)1:205609904G>A
(
Rattus norvegicus
)
Allele/Variant
Source:
rs8167689
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205609904G>A
(mRatBN7.2)1:205610082G>A
(
Rattus norvegicus
)
Allele/Variant
Source:
rs8162831
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
synonymous_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205610082G>A
(mRatBN7.2)1:205617809C>A
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319161251
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205617809C>A
(mRatBN7.2)1:205615527G>T
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319178618
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205615527G>T
(mRatBN7.2)1:205618683C>G
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319166781
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205618683C>G
(mRatBN7.2)1:205611361C>T
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319161263
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205611361C>T
(mRatBN7.2)1:205612178A>T
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319144508
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205612178A>T
(mRatBN7.2)1:205610009C>T
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319183105
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205610009C>T
(mRatBN7.2)1:205610760G>A
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319166997
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205610760G>A
(mRatBN7.2)1:205614382C>G
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319168518
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205614382C>G
(mRatBN7.2)1:205618367T>C
(
Rattus norvegicus
)
Allele/Variant
Source:
NC_051336.1:g.205618367T>C
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205618367T>C
(mRatBN7.2)1:205615583G>A
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319180369
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205615583G>A
(mRatBN7.2)1:205610621A>G
(
Rattus norvegicus
)
Allele/Variant
Source:
rs3319178561
Genes:
Slc3a2 (Rno)
Synonyms:
Not Available
Variant Type:
SNP
Molecular Consequence:
intron_variant
Diseases:
Not Available
Variant Name:
(mRatBN7.2)1:205610621A>G
Page 1 of 1
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