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

(mRatBN7.2)16:69246054G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323000458
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69246054G>C

(mRatBN7.2)16:69246064G>A

(Rattus norvegicus)
Allele/Variant
Source: rs105767132
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69246064G>A

(mRatBN7.2)16:69246166A>G

(Rattus norvegicus)
Allele/Variant
Source: rs106165417
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69246166A>G

(mRatBN7.2)16:69246826A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323029111
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69246826A>G

(mRatBN7.2)16:69247125G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322866494
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69247125G>A

(mRatBN7.2)16:69248503A>G

(Rattus norvegicus)
Allele/Variant
Source: rs199180131
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69248503A>G

(mRatBN7.2)16:69245575A>G

(Rattus norvegicus)
Allele/Variant
Source: rs105282154
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69245575A>G

(mRatBN7.2)16:69255113G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198804215
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69255113G>A

(mRatBN7.2)16:69255889G>A

(Rattus norvegicus)
Allele/Variant
Source: rs197190632
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69255889G>A

(mRatBN7.2)16:69242444C>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323054759
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69242444C>G

(mRatBN7.2)16:69242171A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323000467
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69242171A>C

(mRatBN7.2)16:69242300C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323054744
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69242300C>T

(mRatBN7.2)16:69245199C>A

(Rattus norvegicus)
Allele/Variant
Source: rs104922543
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69245199C>A

(mRatBN7.2)16:69254804G>A

(Rattus norvegicus)
Allele/Variant
Source: rs197987142
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69254804G>A

(mRatBN7.2)16:69254989G>T

(Rattus norvegicus)
Allele/Variant
Source: rs197462966
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69254989G>T

(mRatBN7.2)16:69255050C>T

(Rattus norvegicus)
Allele/Variant
Source: rs199399870
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69255050C>T

(mRatBN7.2)16:69255566G>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051351.1:g.69255566G>T
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69255566G>T

(mRatBN7.2)16:69255689A>G

(Rattus norvegicus)
Allele/Variant
Source: rs198778623
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69255689A>G

(mRatBN7.2)16:69258235G>A

(Rattus norvegicus)
Allele/Variant
Source: rs197819280
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69258235G>A

(mRatBN7.2)16:69258980C>T

(Rattus norvegicus)
Allele/Variant
Source: rs198439135
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69258980C>T

(mRatBN7.2)16:69240833T>C

(Rattus norvegicus)
Allele/Variant
Source: rs13450527
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69240833T>C

(mRatBN7.2)16:69244962A>G

(Rattus norvegicus)
Allele/Variant
Source: rs105431849
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69244962A>G

(mRatBN7.2)16:69254835C>T

(Rattus norvegicus)
Allele/Variant
Source: rs198718684
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69254835C>T

(mRatBN7.2)16:69251125C>T

(Rattus norvegicus)
Allele/Variant
Source: rs199125688
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69251125C>T

(mRatBN7.2)16:69263386C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051351.1:g.69263386C>T
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69263386C>T

(mRatBN7.2)16:69247109G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322625118
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69247109G>T

(mRatBN7.2)16:69253273T>C

(Rattus norvegicus)
Allele/Variant
Source: rs104899832
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69253273T>C

(mRatBN7.2)16:69254384C>T

(Rattus norvegicus)
Allele/Variant
Source: rs198983770
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69254384C>T

(mRatBN7.2)16:69254645T>A

(Rattus norvegicus)
Allele/Variant
Source: rs198241927
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69254645T>A

(mRatBN7.2)16:69263734T>C

(Rattus norvegicus)
Allele/Variant
Source: rs199310782
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69263734T>C

(mRatBN7.2)16:69241606C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322892330
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69241606C>T

(mRatBN7.2)16:69245564C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105814252
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69245564C>T

(mRatBN7.2)16:69250613A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051351.1:g.69250613A>G
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69250613A>G

(mRatBN7.2)16:69251591G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051351.1:g.69251591G>A
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69251591G>A

(mRatBN7.2)16:69253627A>T

(Rattus norvegicus)
Allele/Variant
Source: rs198806241
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69253627A>T

(mRatBN7.2)16:69255856G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198334297
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69255856G>A

(mRatBN7.2)16:69260075T>C

(Rattus norvegicus)
Allele/Variant
Source: rs198340712
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69260075T>C

(mRatBN7.2)16:69262060C>T

(Rattus norvegicus)
Allele/Variant
Source: rs106588951
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69262060C>T

(mRatBN7.2)16:69246829C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323066972
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69246829C>T

(mRatBN7.2)16:69240716C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323000444
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69240716C>T

(mRatBN7.2)16:69245075A>G

(Rattus norvegicus)
Allele/Variant
Source: rs105816205
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69245075A>G

(mRatBN7.2)16:69245214A>G

(Rattus norvegicus)
Allele/Variant
Source: rs107349262
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69245214A>G

(mRatBN7.2)16:69245529G>A

(Rattus norvegicus)
Allele/Variant
Source: rs106505900
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69245529G>A

(mRatBN7.2)16:69245542T>C

(Rattus norvegicus)
Allele/Variant
Source: rs106449213
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69245542T>C

(mRatBN7.2)16:69251804C>G

(Rattus norvegicus)
Allele/Variant
Source: rs105708931
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69251804C>G

(mRatBN7.2)16:69251809T>C

(Rattus norvegicus)
Allele/Variant
Source: rs197284336
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69251809T>C

(mRatBN7.2)16:69252210T>C

(Rattus norvegicus)
Allele/Variant
Source: rs198031549
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69252210T>C

(mRatBN7.2)16:69256068G>C

(Rattus norvegicus)
Allele/Variant
Source: rs105495409
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69256068G>C

(mRatBN7.2)16:69256861T>G

(Rattus norvegicus)
Allele/Variant
Source: rs197306946
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69256861T>G

(mRatBN7.2)16:69257818G>A

(Rattus norvegicus)
Allele/Variant
Source: rs197517427
Genes: Plat (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:69257818G>A