Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: Abl2 (Rno)
(mRatBN7.2)13:68775456C>T
(Rattus norvegicus)Allele/Variant
Source: rs3322383103
Genes: Abl2 (Rno), Tor3a (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68775456C>T
(mRatBN7.2)13:68778990T>A
(Rattus norvegicus)Allele/Variant
Source: rs197074948
Genes: Abl2 (Rno), Tor3a (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68778990T>A
(mRatBN7.2)13:68765183C>T
(Rattus norvegicus)Allele/Variant
Source: rs198057165
Genes: Abl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68765183C>T
(mRatBN7.2)13:68787533T>A
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.68787533T>A
Genes: Abl2 (Rno), Tor3a (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68787533T>A
(mRatBN7.2)13:68787536G>T
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.68787536G>T
Genes: Abl2 (Rno), Tor3a (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68787536G>T
(mRatBN7.2)13:68787851G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.68787851G>A
Genes: Abl2 (Rno), Tor3a (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68787851G>A
(mRatBN7.2)13:68788341T>A
(Rattus norvegicus)Allele/Variant
Source: rs199119668
Genes: Abl2 (Rno), Tor3a (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68788341T>A
(mRatBN7.2)13:68789684A>G
(Rattus norvegicus)Allele/Variant
Source: rs3322383065
Genes: Abl2 (Rno), Tor3a (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68789684A>G
(mRatBN7.2)13:68790282T>A
(Rattus norvegicus)Allele/Variant
Source: rs3322066690
Genes: Abl2 (Rno), Tor3a (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68790282T>A
(mRatBN7.2)13:68714495A>G
(Rattus norvegicus)Allele/Variant
Source: rs3322428867
Genes: Abl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68714495A>G
(mRatBN7.2)13:68816948A>G
(Rattus norvegicus)Allele/Variant
Source: rs3322428910
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68816948A>G
(mRatBN7.2)13:68817920A>G
(Rattus norvegicus)Allele/Variant
Source: rs3322482455
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68817920A>G
(mRatBN7.2)13:68834879T>A
(Rattus norvegicus)Allele/Variant
Source: rs3322235556
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68834879T>A
(mRatBN7.2)13:68835594C>T
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.68835594C>T
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68835594C>T
(mRatBN7.2)13:68718847G>A
(Rattus norvegicus)Allele/Variant
Source: rs3322385740
Genes: Abl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68718847G>A
(mRatBN7.2)13:68723108A>C
(Rattus norvegicus)Allele/Variant
Source: rs3322347647
Genes: Abl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68723108A>C
(mRatBN7.2)13:68724942G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.68724942G>A
Genes: Abl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68724942G>A
(mRatBN7.2)13:68725038C>T
(Rattus norvegicus)Allele/Variant
Source: rs3322408180
Genes: Abl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68725038C>T
(mRatBN7.2)13:68725295T>C
(Rattus norvegicus)Allele/Variant
Source: rs3322403744
Genes: Abl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68725295T>C
(mRatBN7.2)13:68811988G>A
(Rattus norvegicus)Allele/Variant
Source: rs198709027
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68811988G>A
(mRatBN7.2)13:68724978G>T
(Rattus norvegicus)Allele/Variant
Source: rs3322428866
Genes: Abl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68724978G>T
(mRatBN7.2)13:68733608C>T
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.68733608C>T
Genes: Abl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68733608C>T
(mRatBN7.2)13:68729696A>G
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.68729696A>G
Genes: Abl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68729696A>G
(mRatBN7.2)13:68818372C>A
(Rattus norvegicus)Allele/Variant
Source: rs3322381067
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68818372C>A
(mRatBN7.2)13:68822014G>A
(Rattus norvegicus)Allele/Variant
Source: rs198684002
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68822014G>A
(mRatBN7.2)13:68811900C>T
(Rattus norvegicus)Allele/Variant
Source: rs197973315
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68811900C>T
(mRatBN7.2)13:68826923C>G
(Rattus norvegicus)Allele/Variant
Source: rs3322408169
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68826923C>G
(mRatBN7.2)13:68834139A>C
(Rattus norvegicus)Allele/Variant
Source: rs199388894
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68834139A>C
(mRatBN7.2)13:68782512A>G
(Rattus norvegicus)Allele/Variant
Source: rs197723495
Genes: Abl2 (Rno), Tor3a (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68782512A>G
(mRatBN7.2)13:68787041G>A
(Rattus norvegicus)Allele/Variant
Source: rs3322436761
Genes: Abl2 (Rno), Tor3a (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68787041G>A
(mRatBN7.2)13:68786832C>T
(Rattus norvegicus)Allele/Variant
Source: rs3322271908
Genes: Abl2 (Rno), Tor3a (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68786832C>T
(mRatBN7.2)13:68797074A>C
(Rattus norvegicus)Allele/Variant
Source: rs3322407988
Genes: Abl2 (Rno), Tor3a (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68797074A>C
(mRatBN7.2)13:68802880G>A
(Rattus norvegicus)Allele/Variant
Source: rs3322408166
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68802880G>A
(mRatBN7.2)13:68683276A>C
(Rattus norvegicus)Allele/Variant
Source: rs3322403176
Genes: Abl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68683276A>C
(mRatBN7.2)13:68686301C>G
(Rattus norvegicus)Allele/Variant
Source: rs199385288
Genes: Abl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68686301C>G
(mRatBN7.2)13:68688931C>T
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.68688931C>T
Genes: Abl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68688931C>T
(mRatBN7.2)13:68717159G>A
(Rattus norvegicus)Allele/Variant
Source: rs3322066629
Genes: Abl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68717159G>A
(mRatBN7.2)13:68736937T>C
(Rattus norvegicus)Allele/Variant
Source: rs3322383117
Genes: Abl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68736937T>C
(mRatBN7.2)13:68807269C>G
(Rattus norvegicus)Allele/Variant
Source: rs3322066685
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68807269C>G
(mRatBN7.2)13:68814716C>A
(Rattus norvegicus)Allele/Variant
Source: rs198989586
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68814716C>A
(mRatBN7.2)13:68714996T>C
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.68714996T>C
Genes: Abl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68714996T>C
(mRatBN7.2)13:68716991T>A
(Rattus norvegicus)Allele/Variant
Source: rs3322435463
Genes: Abl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68716991T>A
(mRatBN7.2)13:68719730A>G
(Rattus norvegicus)Allele/Variant
Source: rs3322294300
Genes: Abl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68719730A>G
(mRatBN7.2)13:68815258C>A
(Rattus norvegicus)Allele/Variant
Source: rs199269107
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68815258C>A
(mRatBN7.2)13:68825018C>T
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.68825018C>T
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68825018C>T
(mRatBN7.2)13:68809731G>A
(Rattus norvegicus)Allele/Variant
Source: rs3322408175
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68809731G>A
(mRatBN7.2)13:68811978T>C
(Rattus norvegicus)Allele/Variant
Source: rs3322408121
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68811978T>C
(mRatBN7.2)13:68825400G>A
(Rattus norvegicus)Allele/Variant
Source: rs198696929
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68825400G>A
(mRatBN7.2)13:68834355T>C
(Rattus norvegicus)Allele/Variant
Source: rs105043007
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68834355T>C
(mRatBN7.2)13:68834767G>T
(Rattus norvegicus)Allele/Variant
Source: rs104921618
Genes: Abl2 (Rno), Fam20b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:68834767G>T