Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: Sap30l (Rno)
(mRatBN7.2)10:41980113C>T
(Rattus norvegicus)Allele/Variant
Source: rs3321816051
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41980113C>T
(mRatBN7.2)10:41981536T>C
(Rattus norvegicus)Allele/Variant
Source: NC_051345.1:g.41981536T>C
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41981536T>C
(mRatBN7.2)10:41981541T>C
(Rattus norvegicus)Allele/Variant
Source: NC_051345.1:g.41981541T>C
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41981541T>C
(mRatBN7.2)10:41981593A>G
(Rattus norvegicus)Allele/Variant
Source: NC_051345.1:g.41981593A>G
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41981593A>G
(mRatBN7.2)10:41981835C>T
(Rattus norvegicus)Allele/Variant
Source: rs3321690574
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41981835C>T
(mRatBN7.2)10:41982056C>A
(Rattus norvegicus)Allele/Variant
Source: rs3321831030
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41982056C>A
(mRatBN7.2)10:41982080G>T
(Rattus norvegicus)Allele/Variant
Source: NC_051345.1:g.41982080G>T
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41982080G>T
(mRatBN7.2)10:41982317G>A
(Rattus norvegicus)Allele/Variant
Source: rs3321816032
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41982317G>A
(mRatBN7.2)10:41983486A>G
(Rattus norvegicus)Allele/Variant
Source: rs199088707
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41983486A>G
(mRatBN7.2)10:41983628T>C
(Rattus norvegicus)Allele/Variant
Source: rs197163470
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41983628T>C
(mRatBN7.2)10:41980122C>A
(Rattus norvegicus)Allele/Variant
Source: rs3321870537
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41980122C>A
(mRatBN7.2)10:41986895C>T
(Rattus norvegicus)Allele/Variant
Source: rs198082112
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41986895C>T
(mRatBN7.2)10:41981481C>T
(Rattus norvegicus)Allele/Variant
Source: rs3321690551
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41981481C>T
(mRatBN7.2)10:41981990T>A
(Rattus norvegicus)Allele/Variant
Source: rs3321815975
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41981990T>A
(mRatBN7.2)10:41983219C>T
(Rattus norvegicus)Allele/Variant
Source: rs3321690524
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41983219C>T
(mRatBN7.2)10:41986686A>C
(Rattus norvegicus)Allele/Variant
Source: rs197893305
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41986686A>C
(mRatBN7.2)10:41986873C>T
(Rattus norvegicus)Allele/Variant
Source: rs198647341
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41986873C>T
(mRatBN7.2)10:41986897T>C
(Rattus norvegicus)Allele/Variant
Source: rs198606923
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41986897T>C
(mRatBN7.2)10:41980062C>A
(Rattus norvegicus)Allele/Variant
Source: rs197652178
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41980062C>A
(mRatBN7.2)10:41980555T>C
(Rattus norvegicus)Allele/Variant
Source: rs3321722591
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41980555T>C
(mRatBN7.2)10:41981147T>C
(Rattus norvegicus)Allele/Variant
Source: rs199049748
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41981147T>C
(mRatBN7.2)10:41981581A>G
(Rattus norvegicus)Allele/Variant
Source: NC_051345.1:g.41981581A>G
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41981581A>G
(mRatBN7.2)10:41982791G>A
(Rattus norvegicus)Allele/Variant
Source: rs3321833895
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41982791G>A
(mRatBN7.2)10:41981345A>G
(Rattus norvegicus)Allele/Variant
Source: rs199250789
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41981345A>G
(mRatBN7.2)10:41981585G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051345.1:g.41981585G>A
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41981585G>A
(mRatBN7.2)10:41981533T>C
(Rattus norvegicus)Allele/Variant
Source: NC_051345.1:g.41981533T>C
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41981533T>C
(mRatBN7.2)10:41982319C>A
(Rattus norvegicus)Allele/Variant
Source: rs3321815927
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41982319C>A
(mRatBN7.2)10:41982483T>C
(Rattus norvegicus)Allele/Variant
Source: rs197817242
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41982483T>C
(mRatBN7.2)10:41982489T>C
(Rattus norvegicus)Allele/Variant
Source: rs199020117
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41982489T>C
(mRatBN7.2)10:41983322T>C
(Rattus norvegicus)Allele/Variant
Source: rs197906226
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41983322T>C
(mRatBN7.2)10:41985889G>A
(Rattus norvegicus)Allele/Variant
Source: rs3321860274
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41985889G>A
(mRatBN7.2)10:41987053C>T
(Rattus norvegicus)Allele/Variant
Source: NC_051345.1:g.41987053C>T
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41987053C>T
(mRatBN7.2)10:41986875T>C
(Rattus norvegicus)Allele/Variant
Source: rs197399006
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41986875T>C
(mRatBN7.2)10:41987050G>T
(Rattus norvegicus)Allele/Variant
Source: NC_051345.1:g.41987050G>T
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41987050G>T
(mRatBN7.2)10:41987051G>T
(Rattus norvegicus)Allele/Variant
Source: NC_051345.1:g.41987051G>T
Genes: Sap30l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:41987051G>T