Version: 8.0.0
Date: Tue Jan 28 2025
18 results
Allele/Variant Genes: E230025N22Rikl (Rno)

(mRatBN7.2)18:28287390C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323266147
Genes: E230025N22Rikl (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:28287390C>T

(mRatBN7.2)18:28288055T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323127788
Genes: E230025N22Rikl (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:28288055T>G

(mRatBN7.2)18:28291375T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323292378
Genes: E230025N22Rikl (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:28291375T>G

(mRatBN7.2)18:28291693A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323080849
Genes: E230025N22Rikl (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:28291693A>G

(mRatBN7.2)18:28294410C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105623396
Genes: E230025N22Rikl (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:28294410C>T

(mRatBN7.2)18:28294820T>A

(Rattus norvegicus)
Allele/Variant
Source: rs104978589
Genes: E230025N22Rikl (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:28294820T>A

(mRatBN7.2)18:28289010G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3323266279
Genes: E230025N22Rikl (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:28289010G>A

(mRatBN7.2)18:28292462C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323324041
Genes: E230025N22Rikl (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:28292462C>T

(mRatBN7.2)18:28294902A>G

(Rattus norvegicus)
Allele/Variant
Source: rs106750255
Genes: E230025N22Rikl (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:28294902A>G

(mRatBN7.2)18:28290657C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323327685
Genes: E230025N22Rikl (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:28290657C>T

(mRatBN7.2)18:28293474C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323265688
Genes: E230025N22Rikl (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:28293474C>T

(mRatBN7.2)18:28294206G>T

(Rattus norvegicus)
Allele/Variant
Source: rs107004517
Genes: E230025N22Rikl (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:28294206G>T

(mRatBN7.2)18:28290685A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323292419
Genes: E230025N22Rikl (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:28290685A>G

(mRatBN7.2)18:28292394G>A

(Rattus norvegicus)
Allele/Variant
Source: rs105615466
Genes: E230025N22Rikl (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:28292394G>A

(mRatBN7.2)18:28292908C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105243860
Genes: E230025N22Rikl (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:28292908C>T

(mRatBN7.2)18:28291450T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323153776
Genes: E230025N22Rikl (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:28291450T>C

(mRatBN7.2)18:28289263G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322868435
Genes: E230025N22Rikl (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:28289263G>A

(mRatBN7.2)18:28294112A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323266322
Genes: E230025N22Rikl (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:28294112A>G