2,533 results
Allele/Variant Genes: Large1 (Rno)
Allele/Variant
Source: RGD:2313460
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

(mRatBN7.2)19:11652215C>T

(Rattus norvegicus)
Allele/Variant
Source: rs106750767
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11652215C>T

(mRatBN7.2)19:11653446C>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323411209
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11653446C>G

(mRatBN7.2)19:11606154G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3323270773
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11606154G>A

(mRatBN7.2)19:11607070C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323246008
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11607070C>T

(mRatBN7.2)19:11614679T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323245980
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11614679T>C

(mRatBN7.2)19:11620351T>C

(Rattus norvegicus)
Allele/Variant
Source: rs106264975
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11620351T>C

(mRatBN7.2)19:11604190G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3323409885
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11604190G>A

(mRatBN7.2)19:11623822C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105506915
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11623822C>T

(mRatBN7.2)19:11657613A>G

(Rattus norvegicus)
Allele/Variant
Source: rs107206253
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11657613A>G

(mRatBN7.2)19:11645240T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323385039
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11645240T>C

(mRatBN7.2)19:12031487A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323245995
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:12031487A>C

(mRatBN7.2)19:12034152A>C

(Rattus norvegicus)
Allele/Variant
Source: rs105829989
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:12034152A>C

(mRatBN7.2)19:11607124T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323501531
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11607124T>C

(mRatBN7.2)19:11614055C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323379379
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11614055C>T

(mRatBN7.2)19:11618972A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323198965
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11618972A>T

(mRatBN7.2)19:11645122G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3323336053
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11645122G>A

(mRatBN7.2)19:11630868A>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051354.1:g.11630868A>C
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11630868A>C

(mRatBN7.2)19:11631495G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3323335852
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11631495G>A

(mRatBN7.2)19:11632254T>C

(Rattus norvegicus)
Allele/Variant
Source: rs105793095
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11632254T>C

(mRatBN7.2)19:11633055A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322982453
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11633055A>G

(mRatBN7.2)19:11787415T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323198996
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11787415T>C

(mRatBN7.2)19:11800972A>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051354.1:g.11800972A>C
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11800972A>C

(mRatBN7.2)19:11810832C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105455006
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11810832C>T

(mRatBN7.2)19:11855709A>G

(Rattus norvegicus)
Allele/Variant
Source: rs197943624
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11855709A>G

(mRatBN7.2)19:11815796G>T

(Rattus norvegicus)
Allele/Variant
Source: rs105525326
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11815796G>T

(mRatBN7.2)19:11895544T>C

(Rattus norvegicus)
Allele/Variant
Source: rs199227647
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11895544T>C

(mRatBN7.2)19:11828120A>G

(Rattus norvegicus)
Allele/Variant
Source: rs198998053
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11828120A>G

(mRatBN7.2)19:11878378G>T

(Rattus norvegicus)
Allele/Variant
Source: rs197499720
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11878378G>T

(mRatBN7.2)19:11819656T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323447257
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11819656T>G

(mRatBN7.2)19:11819709T>A

(Rattus norvegicus)
Allele/Variant
Source: rs105806438
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11819709T>A

(mRatBN7.2)19:11606091A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323434464
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11606091A>T

(mRatBN7.2)19:11605644T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323379278
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11605644T>C

(mRatBN7.2)19:11635522C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323434476
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11635522C>T

(mRatBN7.2)19:11635593T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323246021
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11635593T>C

(mRatBN7.2)19:11738823C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051354.1:g.11738823C>T
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11738823C>T

(mRatBN7.2)19:11741679A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323379961
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11741679A>G

(mRatBN7.2)19:11743028C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105190007
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11743028C>T

(mRatBN7.2)19:11744010C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197851901
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11744010C>T

(mRatBN7.2)19:11746062T>C

(Rattus norvegicus)
Allele/Variant
Source: rs107421956
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11746062T>C

(mRatBN7.2)19:11795154C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051354.1:g.11795154C>T
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11795154C>T

(mRatBN7.2)19:11662164A>G

(Rattus norvegicus)
Allele/Variant
Source: rs105262312
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11662164A>G

(mRatBN7.2)19:11662416A>T

(Rattus norvegicus)
Allele/Variant
Source: rs198047772
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11662416A>T

(mRatBN7.2)19:11663414T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323411208
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11663414T>C

(mRatBN7.2)19:11663737C>T

(Rattus norvegicus)
Allele/Variant
Source: rs198120052
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11663737C>T

(mRatBN7.2)19:11666196G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3323447187
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11666196G>A

(mRatBN7.2)19:11670295T>C

(Rattus norvegicus)
Allele/Variant
Source: rs199059907
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11670295T>C

(mRatBN7.2)19:11674648C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323198931
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11674648C>T

(mRatBN7.2)19:11720047G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323385015
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11720047G>C

(mRatBN7.2)19:11726311G>A

(Rattus norvegicus)
Allele/Variant
Source: rs107276732
Genes: Large1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:11726311G>A