Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Species: Rattus norvegicus
(mRatBN7.2)16:1757668G>A
(Rattus norvegicus)Allele/Variant
Source: rs3322877033
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1757668G>A
(mRatBN7.2)16:1767662G>A
(Rattus norvegicus)Allele/Variant
Source: rs3322749382
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1767662G>A
(mRatBN7.2)16:1775601C>A
(Rattus norvegicus)Allele/Variant
Source: rs3322902016
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1775601C>A
(mRatBN7.2)16:1720308C>T
(Rattus norvegicus)Allele/Variant
Source: rs3322909295
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1720308C>T
(mRatBN7.2)16:1723154G>A
(Rattus norvegicus)Allele/Variant
Source: rs3322809390
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1723154G>A
(mRatBN7.2)16:1734051G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051351.1:g.1734051G>A
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1734051G>A
(mRatBN7.2)16:1744558G>C
(Rattus norvegicus)Allele/Variant
Source: rs3322850404
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1744558G>C
(mRatBN7.2)16:1757280C>T
(Rattus norvegicus)Allele/Variant
Source: rs3322909282
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1757280C>T
(mRatBN7.2)16:1776814T>A
(Rattus norvegicus)Allele/Variant
Source: rs3322878403
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1776814T>A
(mRatBN7.2)16:1711189G>A
(Rattus norvegicus)Allele/Variant
Source: rs3322679376
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1711189G>A
(mRatBN7.2)16:1775228G>A
(Rattus norvegicus)Allele/Variant
Source: rs3322963116
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1775228G>A
(mRatBN7.2)16:1780171G>A
(Rattus norvegicus)Allele/Variant
Source: rs3322914166
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1780171G>A
(mRatBN7.2)16:1784574G>C
(Rattus norvegicus)Allele/Variant
Source: rs3322858084
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1784574G>C
(mRatBN7.2)16:1711188T>C
(Rattus norvegicus)Allele/Variant
Source: rs3322858096
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1711188T>C
(mRatBN7.2)16:1717605A>G
(Rattus norvegicus)Allele/Variant
Source: rs3322722230
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1717605A>G
(mRatBN7.2)16:1718050C>G
(Rattus norvegicus)Allele/Variant
Source: rs3322853926
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1718050C>G
(mRatBN7.2)16:1670024T>G
(Rattus norvegicus)Allele/Variant
Source: rs3322854163
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1670024T>G
(mRatBN7.2)16:1677644T>C
(Rattus norvegicus)Allele/Variant
Source: rs3322809325
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1677644T>C
(mRatBN7.2)16:1778960A>C
(Rattus norvegicus)Allele/Variant
Source: NC_051351.1:g.1778960A>C
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1778960A>C
(mRatBN7.2)16:1719467A>G
(Rattus norvegicus)Allele/Variant
Source: rs3322749384
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1719467A>G
(mRatBN7.2)16:1749805G>C
(Rattus norvegicus)Allele/Variant
Source: rs3322854234
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1749805G>C
(mRatBN7.2)16:1718446A>T
(Rattus norvegicus)Allele/Variant
Source: rs3322881006
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1718446A>T
(mRatBN7.2)16:1719440T>A
(Rattus norvegicus)Allele/Variant
Source: rs3322877014
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1719440T>A
(mRatBN7.2)16:1721629A>G
(Rattus norvegicus)Allele/Variant
Source: NC_051351.1:g.1721629A>G
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1721629A>G
(mRatBN7.2)16:1728380G>C
(Rattus norvegicus)Allele/Variant
Source: rs3322850447
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1728380G>C
(mRatBN7.2)16:1733682A>G
(Rattus norvegicus)Allele/Variant
Source: NC_051351.1:g.1733682A>G
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1733682A>G
(mRatBN7.2)16:1688182C>T
(Rattus norvegicus)Allele/Variant
Source: rs3322679443
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1688182C>T
(mRatBN7.2)16:1697587T>C
(Rattus norvegicus)Allele/Variant
Source: rs3322749427
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1697587T>C
(mRatBN7.2)16:1703350C>A
(Rattus norvegicus)Allele/Variant
Source: rs3322722336
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1703350C>A
(mRatBN7.2)16:1671861T>C
(Rattus norvegicus)Allele/Variant
Source: NC_051351.1:g.1671861T>C
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1671861T>C
(mRatBN7.2)16:1752108G>A
(Rattus norvegicus)Allele/Variant
Source: rs3322857976
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1752108G>A
(mRatBN7.2)16:1774208G>A
(Rattus norvegicus)Allele/Variant
Source: rs3322880934
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1774208G>A
(mRatBN7.2)16:1778955A>C
(Rattus norvegicus)Allele/Variant
Source: NC_051351.1:g.1778955A>C
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1778955A>C
(mRatBN7.2)16:1784736G>C
(Rattus norvegicus)Allele/Variant
Source: NC_051351.1:g.1784736G>C
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1784736G>C
(mRatBN7.2)16:1780052C>T
(Rattus norvegicus)Allele/Variant
Source: rs3322850481
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1780052C>T
(mRatBN7.2)16:1737981G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051351.1:g.1737981G>A
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1737981G>A
(mRatBN7.2)16:1745158T>A
(Rattus norvegicus)Allele/Variant
Source: rs3322722086
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1745158T>A
(mRatBN7.2)16:1778950A>C
(Rattus norvegicus)Allele/Variant
Source: NC_051351.1:g.1778950A>C
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1778950A>C
(mRatBN7.2)16:1716840G>A
(Rattus norvegicus)Allele/Variant
Source: rs3322850417
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1716840G>A
(mRatBN7.2)16:1717683C>G
(Rattus norvegicus)Allele/Variant
Source: rs3322901978
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1717683C>G
(mRatBN7.2)16:1671911T>C
(Rattus norvegicus)Allele/Variant
Source: rs3322914021
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1671911T>C
(mRatBN7.2)16:1678624C>T
(Rattus norvegicus)Allele/Variant
Source: rs3322722193
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1678624C>T
(mRatBN7.2)16:1780366A>G
(Rattus norvegicus)Allele/Variant
Source: rs3322878457
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1780366A>G
(mRatBN7.2)16:1738638C>A
(Rattus norvegicus)Allele/Variant
Source: rs3322749395
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1738638C>A
(mRatBN7.2)16:1690533T>G
(Rattus norvegicus)Allele/Variant
Source: rs107226887
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1690533T>G
(mRatBN7.2)16:1765898T>C
(Rattus norvegicus)Allele/Variant
Source: rs3322496044
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1765898T>C
(mRatBN7.2)16:1770906G>A
(Rattus norvegicus)Allele/Variant
Source: rs3322881012
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1770906G>A
(mRatBN7.2)16:1773084G>A
(Rattus norvegicus)Allele/Variant
Source: rs3322923842
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1773084G>A
(mRatBN7.2)16:1712110T>C
(Rattus norvegicus)Allele/Variant
Source: rs3322854219
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1712110T>C
(mRatBN7.2)16:1717810G>C
(Rattus norvegicus)Allele/Variant
Source: rs3322495988
Genes: Slmap (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:1717810G>C