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

(mRatBN7.2)12:41926580T>A

(Rattus norvegicus)
Allele/Variant
Source: rs198575398
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41926580T>A

(mRatBN7.2)12:41908106A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322284616
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41908106A>G

(mRatBN7.2)12:41908764T>C

(Rattus norvegicus)
Allele/Variant
Source: rs107526116
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41908764T>C

(mRatBN7.2)12:41914073G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322216605
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41914073G>A

(mRatBN7.2)12:41916682G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322090037
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41916682G>A

(mRatBN7.2)12:41922602G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322284661
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41922602G>A

(mRatBN7.2)12:41922657C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322196390
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41922657C>T

(mRatBN7.2)12:41924271C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322108028
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41924271C>T

(mRatBN7.2)12:41912535A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322196573
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41912535A>G

(mRatBN7.2)12:41918333A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322220527
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41918333A>G

(mRatBN7.2)12:41920847G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322048798
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41920847G>A

(mRatBN7.2)12:41923704A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322090119
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41923704A>G

(mRatBN7.2)12:41911484C>T

(Rattus norvegicus)
Allele/Variant
Source: rs199127216
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41911484C>T

(mRatBN7.2)12:41912735T>C

(Rattus norvegicus)
Allele/Variant
Source: rs197893098
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41912735T>C

(mRatBN7.2)12:41920555T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3322161705
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41920555T>C

(mRatBN7.2)12:41923206G>A

(Rattus norvegicus)
Allele/Variant
Source: rs197011464
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41923206G>A

(mRatBN7.2)12:41912484C>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322284623
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41912484C>G

(mRatBN7.2)12:41912936A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3322216506
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41912936A>C

(mRatBN7.2)12:41918604T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322090072
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41918604T>A

(mRatBN7.2)12:41919587C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322216565
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41919587C>T

(mRatBN7.2)12:41925620C>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322161739
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41925620C>G

(mRatBN7.2)12:41912764T>C

(Rattus norvegicus)
Allele/Variant
Source: rs197342460
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41912764T>C

(mRatBN7.2)12:41921622A>C

(Rattus norvegicus)
Allele/Variant
Source: rs199121197
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41921622A>C

(mRatBN7.2)12:41910539C>T

(Rattus norvegicus)
Allele/Variant
Source: rs198393738
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41910539C>T

(mRatBN7.2)12:41912513G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3322193818
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41912513G>C

(mRatBN7.2)12:41912753G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198688634
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41912753G>A

(mRatBN7.2)12:41915955A>G

(Rattus norvegicus)
Allele/Variant
Source: rs107562802
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41915955A>G

(mRatBN7.2)12:41919395T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3322239881
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41919395T>C

(mRatBN7.2)12:41921061A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322239643
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41921061A>G

(mRatBN7.2)12:41925366C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322216524
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41925366C>T

(mRatBN7.2)12:41911656C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197109681
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41911656C>T

(mRatBN7.2)12:41914595C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322193937
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41914595C>T

(mRatBN7.2)12:41914896G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322284502
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41914896G>A

(mRatBN7.2)12:41915629A>C

(Rattus norvegicus)
Allele/Variant
Source: rs106901355
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41915629A>C

(mRatBN7.2)12:41921060G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3322246881
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41921060G>C

(mRatBN7.2)12:41925321T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322239877
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41925321T>G

(mRatBN7.2)12:41909568C>T

(Rattus norvegicus)
Allele/Variant
Source: rs199041253
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41909568C>T

(mRatBN7.2)12:41917584G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322161677
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41917584G>A

(mRatBN7.2)12:41920581C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322196576
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41920581C>T

(mRatBN7.2)12:41921001A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051347.1:g.41921001A>G
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41921001A>G

(mRatBN7.2)12:41920888C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322241998
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41920888C>A

(mRatBN7.2)12:41925429T>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051347.1:g.41925429T>G
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41925429T>G

(mRatBN7.2)12:41926545G>A

(Rattus norvegicus)
Allele/Variant
Source: rs197405435
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41926545G>A

(mRatBN7.2)12:41926974T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322220574
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41926974T>A

(mRatBN7.2)12:41909790G>A

(Rattus norvegicus)
Allele/Variant
Source: rs106720048
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41909790G>A

(mRatBN7.2)12:41914609A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322216475
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41914609A>G

(mRatBN7.2)12:41916362T>G

(Rattus norvegicus)
Allele/Variant
Source: rs107573700
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41916362T>G

(mRatBN7.2)12:41918432T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322239692
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41918432T>G

(mRatBN7.2)12:41919257G>T

(Rattus norvegicus)
Allele/Variant
Source: rs106259885
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41919257G>T

(mRatBN7.2)12:41923383G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322220614
Genes: Gltp (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:41923383G>A