267 results
Allele/Variant Genes: Gmfb (Mmu) Molecular Consequence: non coding transcript variant
Allele/Variant
Source: rs249468976
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47058311C>T

Allele/Variant
Source: rs215543846
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47059169T>A

Allele/Variant
Source: rs30833317
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47057612G>A

Allele/Variant
Source: rs253350287
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47049424C>T

Allele/Variant
Source: rs30829941
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47050899C>G

Allele/Variant
Source: rs222364076
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47051537A>T

Allele/Variant
Source: rs249122496
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47052523T>C

Allele/Variant
Source: rs30829030
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47052812T>G

Allele/Variant
Source: rs50162437
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47053691T>G

Allele/Variant
Source: rs259072706
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47056294G>A

Allele/Variant
Source: rs30831165
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47050333G>A

Allele/Variant
Source: rs247496426
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47051162G>A

Allele/Variant
Source: rs212760350
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47052223G>A

Allele/Variant
Source: rs228945802
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47054982G>A

Allele/Variant
Source: rs243928557
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47056907A>G

Allele/Variant
Source: rs581914374
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47051498C>A

Allele/Variant
Source: rs30828078
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47054064A>G

Allele/Variant
Source: rs223542856
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47054727C>T

Allele/Variant
Source: rs243883577
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47055173C>T

Allele/Variant
Source: rs30828081
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47053667C>T

Allele/Variant
Source: rs218628289
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47057602G>T

Allele/Variant
Source: rs587203362
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47058328G>T

Allele/Variant
Source: rs260671930
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47059522T>C

Allele/Variant
Source: rs217206101
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47049426T>G

Allele/Variant
Source: rs216041905
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47050766A>C

Allele/Variant
Source: rs215478433
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47051321C>A

Allele/Variant
Source: rs30829024
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47053304C>G

Allele/Variant
Source: rs225635061
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47053569C>G

Allele/Variant
Source: rs235508784
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47055287A>C

Allele/Variant
Source: rs224215437
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47057300T>C

Allele/Variant
Source: rs231306700
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47057911T>C

Allele/Variant
Source: rs52122263
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47058315T>C

Allele/Variant
Source: rs30833315
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47057934C>T

Allele/Variant
Source: rs265597230
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47057886T>A

Allele/Variant
Source: rs258150326
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47058345C>T

Allele/Variant
Source: rs30141166
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47058819G>A

Allele/Variant
Source: rs582359751
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47058322G>T

Allele/Variant
Source: rs581420750
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47058406T>G

Allele/Variant
Source: rs229726461
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47058278C>T

Allele/Variant
Source: rs246778658
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47057629C>T

Allele/Variant
Source: rs237744567
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47058337C>T

Allele/Variant
Source: rs262007364
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47050884T>C

Allele/Variant
Source: rs243559079
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47051129G>T

Allele/Variant
Source: rs229891930
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47051428C>A

Allele/Variant
Source: rs30829033
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47052390C>A

Allele/Variant
Source: rs30834340
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47055114T>C

Allele/Variant
Source: rs48619428
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47053689A>G

Allele/Variant
Source: rs242803308
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47053713T>C

Allele/Variant
Source: rs30828080
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47053954C>A

Allele/Variant
Source: rs579421427
Genes: Gmfb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:47054042T>C