122 results
Allele/Variant Genes: Btbd7 (Rno)

(mRatBN7.2)6:121925111C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320939513
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121925111C>T

(mRatBN7.2)6:122007464T>C

(Rattus norvegicus)
Allele/Variant
Source: rs107356801
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:122007464T>C

(mRatBN7.2)6:122008352T>A

(Rattus norvegicus)
Allele/Variant
Source: rs106590199
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:122008352T>A

(mRatBN7.2)6:121949125G>C

(Rattus norvegicus)
Allele/Variant
Source: rs105894783
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121949125G>C

(mRatBN7.2)6:121997906A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320969164
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121997906A>G

(mRatBN7.2)6:121926878A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320971487
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121926878A>G

(mRatBN7.2)6:121975712T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320952997
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121975712T>A

(mRatBN7.2)6:121986830C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320858598
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121986830C>T

(mRatBN7.2)6:122006110C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320971442
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:122006110C>T

(mRatBN7.2)6:122007282C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320938929
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:122007282C>T

(mRatBN7.2)6:121929995A>T

(Rattus norvegicus)
Allele/Variant
Source: rs198160626
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121929995A>T

(mRatBN7.2)6:121930030A>C

(Rattus norvegicus)
Allele/Variant
Source: rs199185090
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121930030A>C

(mRatBN7.2)6:121929588G>C

(Rattus norvegicus)
Allele/Variant
Source: rs197166627
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121929588G>C

(mRatBN7.2)6:121980745A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320881562
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121980745A>G

(mRatBN7.2)6:122006122A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320952959
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:122006122A>T

(mRatBN7.2)6:121937362C>T

(Rattus norvegicus)
Allele/Variant
Source: rs106315131
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121937362C>T

(mRatBN7.2)6:121997911T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320892431
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121997911T>G

rs197607038

(Rattus norvegicus)
Allele/Variant
Source: rs197607038
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available

(mRatBN7.2)6:122001542C>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320939488
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:122001542C>G

(mRatBN7.2)6:122007138A>G

(Rattus norvegicus)
Allele/Variant
Source: rs104953464
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:122007138A>G

(mRatBN7.2)6:121943057T>G

(Rattus norvegicus)
Allele/Variant
Source: rs107470122
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121943057T>G

(mRatBN7.2)6:121958642C>T

(Rattus norvegicus)
Allele/Variant
Source: rs106897263
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121958642C>T

(mRatBN7.2)6:121967174T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320952770
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121967174T>C

(mRatBN7.2)6:121981890G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320892445
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121981890G>A

(mRatBN7.2)6:121936877T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320892460
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121936877T>C

(mRatBN7.2)6:121978234A>T

(Rattus norvegicus)
Allele/Variant
Source: rs106278447
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121978234A>T

(mRatBN7.2)6:121936710T>G

(Rattus norvegicus)
Allele/Variant
Source: rs105758127
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121936710T>G

(mRatBN7.2)6:121926384G>A

(Rattus norvegicus)
Allele/Variant
Source: rs106334455
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121926384G>A

(mRatBN7.2)6:121941461G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320952973
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121941461G>A

(mRatBN7.2)6:121964108G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320952954
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121964108G>A

(mRatBN7.2)6:121921477A>G

(Rattus norvegicus)
Allele/Variant
Source: rs106170953
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121921477A>G

(mRatBN7.2)6:121929609A>C

(Rattus norvegicus)
Allele/Variant
Source: rs197755505
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121929609A>C

(mRatBN7.2)6:121929641C>G

(Rattus norvegicus)
Allele/Variant
Source: rs199029489
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121929641C>G

(mRatBN7.2)6:121940180T>C

(Rattus norvegicus)
Allele/Variant
Source: rs197343107
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121940180T>C

(mRatBN7.2)6:121951543T>C

(Rattus norvegicus)
Allele/Variant
Source: rs107179606
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121951543T>C

(mRatBN7.2)6:121954455G>A

(Rattus norvegicus)
Allele/Variant
Source: rs106538160
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121954455G>A

(mRatBN7.2)6:121920528A>G

(Rattus norvegicus)
Allele/Variant
Source: rs8151553
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121920528A>G

(mRatBN7.2)6:121923495T>A

(Rattus norvegicus)
Allele/Variant
Source: rs107246097
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121923495T>A

(mRatBN7.2)6:121929437T>C

(Rattus norvegicus)
Allele/Variant
Source: rs197706484
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121929437T>C

(mRatBN7.2)6:122008909G>A

(Rattus norvegicus)
Allele/Variant
Source: rs107074713
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:122008909G>A

(mRatBN7.2)6:121942413A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051341.1:g.121942413A>G
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121942413A>G

(mRatBN7.2)6:121930712T>G

(Rattus norvegicus)
Allele/Variant
Source: rs107478077
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121930712T>G

(mRatBN7.2)6:121935467A>G

(Rattus norvegicus)
Allele/Variant
Source: rs64838863
Genes: Btbd7 (Rno), LOC100912037 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121935467A>G

(mRatBN7.2)6:121925115A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320939453
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121925115A>C

(mRatBN7.2)6:122010089T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320763347
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:122010089T>C

(mRatBN7.2)6:121922226G>T

(Rattus norvegicus)
Allele/Variant
Source: rs106000635
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121922226G>T

(mRatBN7.2)6:121987540T>A

(Rattus norvegicus)
Allele/Variant
Source: rs105419394
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121987540T>A

(mRatBN7.2)6:121939597T>C

(Rattus norvegicus)
Allele/Variant
Source: rs105138482
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121939597T>C

(mRatBN7.2)6:121968065G>C

(Rattus norvegicus)
Allele/Variant
Source: rs107492621
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:121968065G>C

(mRatBN7.2)6:122007284C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320979693
Genes: Btbd7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:122007284C>T