11,279 results
Allele/Variant Genes: 2210408I21Rik (Mmu)

2210408I21Rikem1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7309172
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

2210408I21Rikem11Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7309171
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: MGI:4434390
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: MGI:5692716
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs227497638
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77284306T>C

Allele/Variant
Source: rs48550366
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77284897C>T

Allele/Variant
Source: rs51928680
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77284998A>C

Allele/Variant
Source: rs212283459
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77285259G>A

Allele/Variant
Source: rs234316843
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77285867A>G

Allele/Variant
Source: rs237428380
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77285980C>T

Allele/Variant
Source: rs216169243
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77286374G>A

Allele/Variant
Source: rs226387537
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77287198G>C

Allele/Variant
Source: rs250637537
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77283921C>G

Allele/Variant
Source: rs234822949
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77284550T>C

Allele/Variant
Source: rs48889362
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77609461G>A

Allele/Variant
Source: rs47618297
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77609475A>G

Allele/Variant
Source: rs47590549
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77609517G>A

Allele/Variant
Source: rs245297590
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77609959G>T

Allele/Variant
Source: rs251915200
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77610173T>C

Allele/Variant
Source: rs212474204
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77610265T>C

Allele/Variant
Source: rs263323380
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77606308T>A

Allele/Variant
Source: rs242951560
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77607353T>A

Allele/Variant
Source: rs256472161
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77612052A>G

Allele/Variant
Source: rs243431893
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77612274C>G

Allele/Variant
Source: rs250722008
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77421784A>T

Allele/Variant
Source: rs234934773
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77422667T>C

Allele/Variant
Source: rs47824589
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77422713C>T

Allele/Variant
Source: rs216112101
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77423738G>A

Allele/Variant
Source: rs107791144
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77424146A>G

Allele/Variant
Source: rs245103389
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77424437A>C

Allele/Variant
Source: rs215986538
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77424439A>C

Allele/Variant
Source: rs224738638
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77429949G>T

Allele/Variant
Source: rs235398923
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77433647C>T

Allele/Variant
Source: rs108725574
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77426590C>T

Allele/Variant
Source: rs247989506
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77284367G>A

Allele/Variant
Source: rs227557733
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77284589T>A

Allele/Variant
Source: rs50799512
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77284735T>G

Allele/Variant
Source: rs254551145
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77285206C>T

Allele/Variant
Source: rs251544601
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77285323C>T

Allele/Variant
Source: rs255648769
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77285999A>G

Allele/Variant
Source: rs46598752
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77286879A>C

Allele/Variant
Source: rs231535441
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77286897C>T

Allele/Variant
Source: rs221354985
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77286969T>C

Allele/Variant
Source: rs580317983
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77288051C>T

Allele/Variant
Source: rs50252415
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77285169T>G

Allele/Variant
Source: rs48963178
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77284951T>C

Allele/Variant
Source: rs255098895
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77285074C>T

Allele/Variant
Source: rs234039996
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77285451C>A

Allele/Variant
Source: rs212379265
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77285761C>G

Allele/Variant
Source: rs232805599
Genes: 2210408I21Rik (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:77286278C>T