Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: Wars2 (Rno)
(mRatBN7.2)2:186463363C>T
(Rattus norvegicus)Allele/Variant
Source: NC_051337.1:g.186463363C>T
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186463363C>T
(mRatBN7.2)2:186482215A>T
(Rattus norvegicus)Allele/Variant
Source: rs3319652757
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186482215A>T
(mRatBN7.2)2:186502672C>T
(Rattus norvegicus)Allele/Variant
Source: rs3319616714
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186502672C>T
(mRatBN7.2)2:186504145G>A
(Rattus norvegicus)Allele/Variant
Source: rs3319640618
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186504145G>A
(mRatBN7.2)2:186520302T>C
(Rattus norvegicus)Allele/Variant
Source: NC_051337.1:g.186520302T>C
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186520302T>C
(mRatBN7.2)2:186521694T>C
(Rattus norvegicus)Allele/Variant
Source: NC_051337.1:g.186521694T>C
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186521694T>C
(mRatBN7.2)2:186491389C>T
(Rattus norvegicus)Allele/Variant
Source: NC_051337.1:g.186491389C>T
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186491389C>T
(mRatBN7.2)2:186476811G>T
(Rattus norvegicus)Allele/Variant
Source: rs107240815
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186476811G>T
(mRatBN7.2)2:186479714T>C
(Rattus norvegicus)Allele/Variant
Source: NC_051337.1:g.186479714T>C
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186479714T>C
(mRatBN7.2)2:186483364C>T
(Rattus norvegicus)Allele/Variant
Source: rs3319618433
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186483364C>T
(mRatBN7.2)2:186529099C>G
(Rattus norvegicus)Allele/Variant
Source: NC_051337.1:g.186529099C>G
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186529099C>G
(mRatBN7.2)2:186470286T>C
(Rattus norvegicus)Allele/Variant
Source: rs197996022
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186470286T>C
(mRatBN7.2)2:186475715C>T
(Rattus norvegicus)Allele/Variant
Source: rs198313432
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186475715C>T
(mRatBN7.2)2:186486590G>A
(Rattus norvegicus)Allele/Variant
Source: rs3319658328
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186486590G>A
(mRatBN7.2)2:186488725G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051337.1:g.186488725G>A
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186488725G>A
(mRatBN7.2)2:186535342G>C
(Rattus norvegicus)Allele/Variant
Source: rs3319639398
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186535342G>C
(mRatBN7.2)2:186535626G>T
(Rattus norvegicus)Allele/Variant
Source: NC_051337.1:g.186535626G>T
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186535626G>T
(mRatBN7.2)2:186541062C>T
(Rattus norvegicus)Allele/Variant
Source: rs105295613
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186541062C>T
(mRatBN7.2)2:186477561G>A
(Rattus norvegicus)Allele/Variant
Source: rs106055039
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186477561G>A
(mRatBN7.2)2:186517096G>A
(Rattus norvegicus)Allele/Variant
Source: rs3319647499
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186517096G>A
(mRatBN7.2)2:186466805G>T
(Rattus norvegicus)Allele/Variant
Source: rs3319618318
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186466805G>T
(mRatBN7.2)2:186472965G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051337.1:g.186472965G>A
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186472965G>A
(mRatBN7.2)2:186473387G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051337.1:g.186473387G>A
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186473387G>A
(mRatBN7.2)2:186476674T>A
(Rattus norvegicus)Allele/Variant
Source: rs105635948
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186476674T>A
(mRatBN7.2)2:186484980C>T
(Rattus norvegicus)Allele/Variant
Source: rs3319647537
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186484980C>T
(mRatBN7.2)2:186485006T>A
(Rattus norvegicus)Allele/Variant
Source: rs3319652805
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186485006T>A
(mRatBN7.2)2:186485588G>C
(Rattus norvegicus)Allele/Variant
Source: rs3319652660
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186485588G>C
(mRatBN7.2)2:186487152G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051337.1:g.186487152G>A
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186487152G>A
(mRatBN7.2)2:186491397G>A
(Rattus norvegicus)Allele/Variant
Source: rs3319570090
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186491397G>A
(mRatBN7.2)2:186518754A>T
(Rattus norvegicus)Allele/Variant
Source: rs3319651282
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186518754A>T
(mRatBN7.2)2:186468239G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051337.1:g.186468239G>A
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186468239G>A
(mRatBN7.2)2:186471805A>G
(Rattus norvegicus)Allele/Variant
Source: rs3319618375
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186471805A>G
(mRatBN7.2)2:186484793A>C
(Rattus norvegicus)Allele/Variant
Source: rs3319658283
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186484793A>C
(mRatBN7.2)2:186486620C>T
(Rattus norvegicus)Allele/Variant
Source: NC_051337.1:g.186486620C>T
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186486620C>T
(mRatBN7.2)2:186493834A>G
(Rattus norvegicus)Allele/Variant
Source: rs3319570133
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186493834A>G
(mRatBN7.2)2:186495578T>C
(Rattus norvegicus)Allele/Variant
Source: rs3323580074
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186495578T>C
(mRatBN7.2)2:186496424G>A
(Rattus norvegicus)Allele/Variant
Source: rs3319653570
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186496424G>A
(mRatBN7.2)2:186499271T>C
(Rattus norvegicus)Allele/Variant
Source: rs3319640582
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186499271T>C
(mRatBN7.2)2:186540279T>C
(Rattus norvegicus)Allele/Variant
Source: rs105960376
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186540279T>C
(mRatBN7.2)2:186528835G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051337.1:g.186528835G>A
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186528835G>A
(mRatBN7.2)2:186500192C>A
(Rattus norvegicus)Allele/Variant
Source: rs197873779
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186500192C>A
(mRatBN7.2)2:186509819C>T
(Rattus norvegicus)Allele/Variant
Source: rs3319616774
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186509819C>T
(mRatBN7.2)2:186509927A>T
(Rattus norvegicus)Allele/Variant
Source: rs3319651235
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186509927A>T
(mRatBN7.2)2:186537117G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051337.1:g.186537117G>A
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186537117G>A
(mRatBN7.2)2:186467687C>T
(Rattus norvegicus)Allele/Variant
Source: rs105884827
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186467687C>T
(mRatBN7.2)2:186474629G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051337.1:g.186474629G>A
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186474629G>A
(mRatBN7.2)2:186486361C>T
(Rattus norvegicus)Allele/Variant
Source: NC_051337.1:g.186486361C>T
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186486361C>T
(mRatBN7.2)2:186487234C>T
(Rattus norvegicus)Allele/Variant
Source: rs199095592
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186487234C>T
(mRatBN7.2)2:186489592C>A
(Rattus norvegicus)Allele/Variant
Source: rs3319653602
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186489592C>A
(mRatBN7.2)2:186494616T>C
(Rattus norvegicus)Allele/Variant
Source: rs197277011
Genes: Wars2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)2:186494616T>C