34 results
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