50 results
Allele/Variant Genes: Myf6 (Mmu)

Myf6tm1(cre)Mrc

(Mus musculus)
Allele/Variant
Source: MGI:3487371
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: alveolar rhabdomyosarcoma
Variant Name: Not Available

Myf6em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7302666
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Myf6tm1Eno

(Mus musculus)
Allele/Variant
Source: MGI:1913092
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Myf6em2Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7376890
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Myf6em1(cre/ERT2)Smoc

(Mus musculus)
Allele/Variant
Source: MGI:6728802
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Myf6tm2(cre)Mrc

(Mus musculus)
Allele/Variant
Source: MGI:3783305
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Myf6tm1Tajb

(Mus musculus)
Allele/Variant
Source: MGI:3055352
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: MGI:5620013
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: MGI:5688769
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Myf6tm1Thbr

(Mus musculus)
Allele/Variant
Source: MGI:1927607
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Myf6tm1Wb

(Mus musculus)
Allele/Variant
Source: MGI:1857220
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs30611318
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329401A>C

Allele/Variant
Source: rs584909182
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329536G>A

Allele/Variant
Source: rs8258515
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329783G>A

Allele/Variant
Source: rs1132465096
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107330401G>C

Allele/Variant
Source: rs579329232
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329529G>A

Allele/Variant
Source: rs584749265
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329519G>A

Allele/Variant
Source: rs8258514
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329861T>C

Allele/Variant
Source: rs8258513
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329946G>C

Allele/Variant
Source: rs30611314
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329114C>T

Allele/Variant
Source: rs30611316
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329373T>C

Allele/Variant
Source: rs16799522
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329497C>T

Allele/Variant
Source: rs248478552
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107328859T>A

Allele/Variant
Source: rs8258524
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329214G>A

Allele/Variant
Source: rs257293555
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329395G>A

Allele/Variant
Source: rs262640148
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107328820G>A

Allele/Variant
Source: rs241790485
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329023C>T

Allele/Variant
Source: rs8258516
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329631G>A

Allele/Variant
Source: rs261328925
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329947C>T

Allele/Variant
Source: rs222946783
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107328824C>T

Allele/Variant
Source: rs225081571
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107330037A>C

Allele/Variant
Source: rs8258523
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329072A>C

Allele/Variant
Source: rs265058044
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329125A>G

Allele/Variant
Source: rs262298902
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107330032C>T

Allele/Variant
Source: rs239202844
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107330095C>T

Allele/Variant
Source: rs8258512
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107330134T>C

Allele/Variant
Source: rs236554476
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329457G>A

Allele/Variant
Source: rs579099280
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329625A>T

Allele/Variant
Source: rs252488766
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107328870G>A

Allele/Variant
Source: rs213020582
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329434A>G

Allele/Variant
Source: rs582248361
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329532C>T

Allele/Variant
Source: rs246683927
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329984A>G

Allele/Variant
Source: rs30610451
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329017C>G

Allele/Variant
Source: rs219889054
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329099A>T

Allele/Variant
Source: rs246847037
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329408C>T

Allele/Variant
Source: rs30611320
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329980A>T

Allele/Variant
Source: rs234992035
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107328804T>C

Allele/Variant
Source: rs1133957303
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107330060G>A

Allele/Variant
Source: rs235149004
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329834G>A

Allele/Variant
Source: rs223154812
Genes: Myf6 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:107329932G>A