Version: 8.0.0
Date: Tue Jan 28 2025
124 results
Allele/Variant Genes: Scyl2 (Rno)

(mRatBN7.2)7:24088563T>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.24088563T>C
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24088563T>C

(mRatBN7.2)7:24114934G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321067172
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24114934G>C

(mRatBN7.2)7:24103641C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321081045
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24103641C>T

(mRatBN7.2)7:24106565G>A

(Rattus norvegicus)
Allele/Variant
Source: rs106275484
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24106565G>A

(mRatBN7.2)7:24110895T>C

(Rattus norvegicus)
Allele/Variant
Source: rs106512890
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24110895T>C

(mRatBN7.2)7:24113360A>G

(Rattus norvegicus)
Allele/Variant
Source: rs107254867
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24113360A>G

(mRatBN7.2)7:24070097A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.24070097A>G
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24070097A>G

(mRatBN7.2)7:24104498G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320960762
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24104498G>A

(mRatBN7.2)7:24117017T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321042044
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24117017T>C

(mRatBN7.2)7:24093407C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.24093407C>T
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24093407C>T

(mRatBN7.2)7:24075906T>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.24075906T>A
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24075906T>A

(mRatBN7.2)7:24077076A>G

(Rattus norvegicus)
Allele/Variant
Source: rs105954685
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24077076A>G

(mRatBN7.2)7:24077080G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321021161
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24077080G>A

(mRatBN7.2)7:24077100G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.24077100G>A
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24077100G>A

(mRatBN7.2)7:24079748C>T

(Rattus norvegicus)
Allele/Variant
Source: rs107367208
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24079748C>T

(mRatBN7.2)7:24114913C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320951653
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24114913C>T

(mRatBN7.2)7:24092823G>C

(Rattus norvegicus)
Allele/Variant
Source: rs105816252
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24092823G>C

(mRatBN7.2)7:24069797C>T

(Rattus norvegicus)
Allele/Variant
Source: rs107148048
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24069797C>T

(mRatBN7.2)7:24071642C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321036160
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24071642C>T

(mRatBN7.2)7:24072288C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321081241
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24072288C>T

(mRatBN7.2)7:24088033C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320838752
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24088033C>T

(mRatBN7.2)7:24093399C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.24093399C>T
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24093399C>T

(mRatBN7.2)7:24077106A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.24077106A>G
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24077106A>G

(mRatBN7.2)7:24077130A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.24077130A>G
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24077130A>G

(mRatBN7.2)7:24082875A>C

(Rattus norvegicus)
Allele/Variant
Source: rs106446417
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24082875A>C

(mRatBN7.2)7:24086455C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321020500
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24086455C>T

(mRatBN7.2)7:24077152A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.24077152A>G
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24077152A>G

(mRatBN7.2)7:24077262A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.24077262A>G
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24077262A>G

(mRatBN7.2)7:24078017G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320838772
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24078017G>A

(mRatBN7.2)7:24078196G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321042107
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24078196G>A

(mRatBN7.2)7:24068942A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3321081178
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24068942A>G

(mRatBN7.2)7:24072239C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323689586
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24072239C>T

(mRatBN7.2)7:24079735G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321056005
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24079735G>C

(mRatBN7.2)7:24082872A>C

(Rattus norvegicus)
Allele/Variant
Source: rs107483315
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24082872A>C

(mRatBN7.2)7:24088490C>G

(Rattus norvegicus)
Allele/Variant
Source: rs3321021148
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24088490C>G

(mRatBN7.2)7:24091270T>A

(Rattus norvegicus)
Allele/Variant
Source: rs106133826
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24091270T>A

(mRatBN7.2)7:24114967T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320926498
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24114967T>C

(mRatBN7.2)7:24098935A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321060190
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24098935A>C

(mRatBN7.2)7:24105273G>A

(Rattus norvegicus)
Allele/Variant
Source: rs105472746
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24105273G>A

(mRatBN7.2)7:24087907A>G

(Rattus norvegicus)
Allele/Variant
Source: rs105596613
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24087907A>G

(mRatBN7.2)7:24093677T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321020383
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24093677T>C

(mRatBN7.2)7:24095707G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321042135
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24095707G>A

(mRatBN7.2)7:24097508C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320951734
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24097508C>A

(mRatBN7.2)7:24100211G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320960639
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24100211G>C

(mRatBN7.2)7:24103270C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320838811
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24103270C>T

(mRatBN7.2)7:24106915C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321060209
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24106915C>T

(mRatBN7.2)7:24109009T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321021064
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24109009T>A

(mRatBN7.2)7:24076783C>A

(Rattus norvegicus)
Allele/Variant
Source: rs104904121
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24076783C>A

(mRatBN7.2)7:24077104A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.24077104A>G
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24077104A>G

(mRatBN7.2)7:24077114A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051342.1:g.24077114A>G
Genes: Scyl2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)7:24077114A>G