867 results
Allele/Variant Genes: Greb1l (Rno)

(mRatBN7.2)18:1433960C>A

(Rattus norvegicus)
Allele/Variant
Source: rs196964281
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1433960C>A

(mRatBN7.2)18:1439095A>G

(Rattus norvegicus)
Allele/Variant
Source: rs197586727
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1439095A>G

(mRatBN7.2)18:1401636C>T

(Rattus norvegicus)
Allele/Variant
Source: rs198301702
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1401636C>T

(mRatBN7.2)18:1404267G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198825452
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1404267G>A

(mRatBN7.2)18:1411221C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3323271404
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1411221C>A

(mRatBN7.2)18:1421513T>G

(Rattus norvegicus)
Allele/Variant
Source: rs198173109
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1421513T>G

(mRatBN7.2)18:1424427T>G

(Rattus norvegicus)
Allele/Variant
Source: rs104948942
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1424427T>G

(mRatBN7.2)18:1428783C>T

(Rattus norvegicus)
Allele/Variant
Source: rs199336402
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1428783C>T

(mRatBN7.2)18:1433382A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051353.1:g.1433382A>G
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1433382A>G

(mRatBN7.2)18:1513647T>A

(Rattus norvegicus)
Allele/Variant
Source: rs107373109
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1513647T>A

(mRatBN7.2)18:1393526T>G

(Rattus norvegicus)
Allele/Variant
Source: rs197452649
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1393526T>G

(mRatBN7.2)18:1464072C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105992949
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1464072C>T

(mRatBN7.2)18:1470935G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198498475
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1470935G>A

(mRatBN7.2)18:1480872A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323236261
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1480872A>G

(mRatBN7.2)18:1422518T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323271423
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1422518T>G

(mRatBN7.2)18:1431553G>C

(Rattus norvegicus)
Allele/Variant
Source: rs105426546
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1431553G>C

(mRatBN7.2)18:1414779A>G

(Rattus norvegicus)
Allele/Variant
Source: rs197172683
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1414779A>G

(mRatBN7.2)18:1512496A>G

(Rattus norvegicus)
Allele/Variant
Source: rs198742015
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1512496A>G

(mRatBN7.2)18:1560204A>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051353.1:g.1560204A>C
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1560204A>C

(mRatBN7.2)18:1563153G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051353.1:g.1563153G>A
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1563153G>A

(mRatBN7.2)18:1396268C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322814318
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1396268C>T

(mRatBN7.2)18:1418164T>C

(Rattus norvegicus)
Allele/Variant
Source: rs198439913
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1418164T>C

(mRatBN7.2)18:1420546C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323321481
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1420546C>T

(mRatBN7.2)18:1473899A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323271425
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1473899A>G

(mRatBN7.2)18:1432349C>T

(Rattus norvegicus)
Allele/Variant
Source: rs198417632
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1432349C>T

(mRatBN7.2)18:1415295A>G

(Rattus norvegicus)
Allele/Variant
Source: rs199280676
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1415295A>G

(mRatBN7.2)18:1514034G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3323268412
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1514034G>A

(mRatBN7.2)18:1523426A>G

(Rattus norvegicus)
Allele/Variant
Source: rs198733782
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1523426A>G

(mRatBN7.2)18:1523649T>C

(Rattus norvegicus)
Allele/Variant
Source: rs198074216
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1523649T>C

(mRatBN7.2)18:1556885C>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051353.1:g.1556885C>A
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1556885C>A

(mRatBN7.2)18:1416786A>G

(Rattus norvegicus)
Allele/Variant
Source: rs198847388
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1416786A>G

(mRatBN7.2)18:1417535G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323203145
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1417535G>T

(mRatBN7.2)18:1417612G>T

(Rattus norvegicus)
Allele/Variant
Source: rs198971629
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1417612G>T

(mRatBN7.2)18:1420502A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323161191
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1420502A>G

(mRatBN7.2)18:1465521G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322814296
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1465521G>A

(mRatBN7.2)18:1478955A>G

(Rattus norvegicus)
Allele/Variant
Source: rs199026053
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1478955A>G

(mRatBN7.2)18:1486249G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3323208366
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1486249G>A

(mRatBN7.2)18:1429708T>C

(Rattus norvegicus)
Allele/Variant
Source: rs63820885
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1429708T>C

(mRatBN7.2)18:1414861G>A

(Rattus norvegicus)
Allele/Variant
Source: rs197903638
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1414861G>A

(mRatBN7.2)18:1585742G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323321498
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1585742G>T

(mRatBN7.2)18:1514347C>T

(Rattus norvegicus)
Allele/Variant
Source: rs106334478
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1514347C>T

(mRatBN7.2)18:1557098A>T

(Rattus norvegicus)
Allele/Variant
Source: rs105214842
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1557098A>T

(mRatBN7.2)18:1561232C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051353.1:g.1561232C>T
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1561232C>T

(mRatBN7.2)18:1565296G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3323070977
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1565296G>A

(mRatBN7.2)18:1551527C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051353.1:g.1551527C>T
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1551527C>T

(mRatBN7.2)18:1551815T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3323268393
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1551815T>A

(mRatBN7.2)18:1392755G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323271410
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1392755G>T

(mRatBN7.2)18:1394027G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198071798
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1394027G>A

(mRatBN7.2)18:1396938T>C

(Rattus norvegicus)
Allele/Variant
Source: rs199281910
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1396938T>C

(mRatBN7.2)18:1398350C>G

(Rattus norvegicus)
Allele/Variant
Source: rs197752345
Genes: Greb1l (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)18:1398350C>G