Version: 8.0.0
Date: Tue Jan 28 2025
60 results
Allele/Variant Genes: Sod2 (Rno)

(mRatBN7.2)1:47640251A>T

(Rattus norvegicus)
Allele/Variant
Source: rs106836631
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47640251A>T

(mRatBN7.2)1:47641036T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3318886128
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47641036T>A

(mRatBN7.2)1:47637434A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3318881538
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47637434A>G

(mRatBN7.2)1:47641676G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3318883029
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47641676G>C

(mRatBN7.2)1:47642611A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3318885301
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47642611A>G

(mRatBN7.2)1:47638228A>G

(Rattus norvegicus)
Allele/Variant
Source: rs107502215
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47638228A>G

(mRatBN7.2)1:47638547C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3318885809
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47638547C>T

(mRatBN7.2)1:47639891A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3318883011
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47639891A>G

(mRatBN7.2)1:47641913T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3318884783
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47641913T>G

(mRatBN7.2)1:47637005T>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.47637005T>C
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47637005T>C

(mRatBN7.2)1:47637310G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.47637310G>A
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47637310G>A

(mRatBN7.2)1:47640911T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3318886080
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47640911T>A

(mRatBN7.2)1:47641073T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3318883822
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47641073T>C

(mRatBN7.2)1:47642690C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3318886039
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47642690C>T

(mRatBN7.2)1:47642694C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3318884548
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47642694C>T

(mRatBN7.2)1:47643858C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.47643858C>T
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47643858C>T

(mRatBN7.2)1:47639145A>G

(Rattus norvegicus)
Allele/Variant
Source: rs106382767
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47639145A>G

(mRatBN7.2)1:47642197G>C

(Rattus norvegicus)
Allele/Variant
Source: rs106776177
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47642197G>C

(mRatBN7.2)1:47642692C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3318883825
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47642692C>T

(mRatBN7.2)1:47644931G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3318885845
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47644931G>A

(mRatBN7.2)1:47645017C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3318887429
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47645017C>A

(mRatBN7.2)1:47640267G>A

(Rattus norvegicus)
Allele/Variant
Source: rs107200446
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47640267G>A

(mRatBN7.2)1:47642753T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3318885350
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47642753T>G

(mRatBN7.2)1:47642770T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3318884459
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47642770T>C

(mRatBN7.2)1:47641520C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.47641520C>T
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47641520C>T

(mRatBN7.2)1:47642711G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3318884743
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47642711G>A

(mRatBN7.2)1:47642435G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3318884760
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47642435G>C

(mRatBN7.2)1:47642496C>G

(Rattus norvegicus)
Allele/Variant
Source: rs3318878410
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47642496C>G

(mRatBN7.2)1:47643259C>A

(Rattus norvegicus)
Allele/Variant
Source: rs105634202
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47643259C>A

(mRatBN7.2)1:47641473A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.47641473A>G
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47641473A>G

(mRatBN7.2)1:47638592T>C

(Rattus norvegicus)
Allele/Variant
Source: rs13457370
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47638592T>C

(mRatBN7.2)1:47640313C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105876014
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47640313C>T

(mRatBN7.2)1:47641617A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3318887108
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47641617A>G

(mRatBN7.2)1:47642731G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3318883093
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47642731G>A

(mRatBN7.2)1:47638588A>G

(Rattus norvegicus)
Allele/Variant
Source: rs13458002
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47638588A>G

(mRatBN7.2)1:47641258A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3318886766
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47641258A>G

(mRatBN7.2)1:47641564C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3318878462
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47641564C>A

(mRatBN7.2)1:47641736A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3318883002
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47641736A>T

(mRatBN7.2)1:47642705A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.47642705A>G
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47642705A>G

(mRatBN7.2)1:47642943T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3318884803
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47642943T>C

(mRatBN7.2)1:47636712G>A

(Rattus norvegicus)
Allele/Variant
Source: rs106517255
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47636712G>A

(mRatBN7.2)1:47643832G>A

(Rattus norvegicus)
Allele/Variant
Source: rs106260082
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47643832G>A

(mRatBN7.2)1:47636686C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3318881534
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47636686C>T

(mRatBN7.2)1:47636715C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105900360
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47636715C>T

(mRatBN7.2)1:47639228G>C

(Rattus norvegicus)
Allele/Variant
Source: rs105392882
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47639228G>C

(mRatBN7.2)1:47640000T>G

(Rattus norvegicus)
Allele/Variant
Source: rs105378140
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47640000T>G

(mRatBN7.2)1:47637894C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105975204
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47637894C>T

(mRatBN7.2)1:47639963A>G

(Rattus norvegicus)
Allele/Variant
Source: rs106699977
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47639963A>G

(mRatBN7.2)1:47641061C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3318885218
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47641061C>T

(mRatBN7.2)1:47636701T>C

(Rattus norvegicus)
Allele/Variant
Source: rs105785426
Genes: Sod2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:47636701T>C