Version: 8.0.0
Date: Tue Jan 28 2025
506 results
Allele/Variant Genes: Mettl14 (Mmu)

(GRCm39)3:123165508T>G

(Mus musculus)
Allele/Variant
Source: rs50243112
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123165508T>G

(GRCm39)3:123165518G>C

(Mus musculus)
Allele/Variant
Source: rs250578697
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123165518G>C

(GRCm39)3:123170309A>T

(Mus musculus)
Allele/Variant
Source: rs233419093
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123170309A>T

(GRCm39)3:123162105T>C

(Mus musculus)
Allele/Variant
Source: rs864280786
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123162105T>C

(GRCm39)3:123179450C>G

(Mus musculus)
Allele/Variant
Source: rs37754466
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123179450C>G

(GRCm39)3:123166738C>T

(Mus musculus)
Allele/Variant
Source: rs228546753
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123166738C>T

(GRCm39)3:123164985T>C

(Mus musculus)
Allele/Variant
Source: rs30853879
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123164985T>C

(GRCm39)3:123165500A>C

(Mus musculus)
Allele/Variant
Source: rs31128012
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123165500A>C

(GRCm39)3:123170215T>G

(Mus musculus)
Allele/Variant
Source: rs227281723
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123170215T>G

(GRCm39)3:123170430T>C

(Mus musculus)
Allele/Variant
Source: rs37433407
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123170430T>C

(GRCm39)3:123170466C>T

(Mus musculus)
Allele/Variant
Source: rs225075330
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123170466C>T

(GRCm39)3:123166378T>A

(Mus musculus)
Allele/Variant
Source: rs220873105
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123166378T>A

(GRCm39)3:123168024T>A

(Mus musculus)
Allele/Variant
Source: rs214896083
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123168024T>A

(GRCm39)3:123168104C>A

(Mus musculus)
Allele/Variant
Source: rs232480687
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123168104C>A

(GRCm39)3:123169460C>G

(Mus musculus)
Allele/Variant
Source: rs262431692
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123169460C>G

(GRCm39)3:123169741A>T

(Mus musculus)
Allele/Variant
Source: rs36777383
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123169741A>T

(GRCm39)3:123171612G>A

(Mus musculus)
Allele/Variant
Source: rs216764978
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123171612G>A

(GRCm39)3:123176780C>T

(Mus musculus)
Allele/Variant
Source: rs221960780
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123176780C>T

(GRCm39)3:123178173C>T

(Mus musculus)
Allele/Variant
Source: rs233581344
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123178173C>T

(GRCm39)3:123178256A>G

(Mus musculus)
Allele/Variant
Source: rs30796315
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123178256A>G

(GRCm39)3:123178333C>A

(Mus musculus)
Allele/Variant
Source: rs235733716
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123178333C>A

(GRCm39)3:123178524A>C

(Mus musculus)
Allele/Variant
Source: rs51756745
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123178524A>C

(GRCm39)3:123179039G>T

(Mus musculus)
Allele/Variant
Source: rs39011099
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123179039G>T

(GRCm39)3:123179092A>G

(Mus musculus)
Allele/Variant
Source: rs45791751
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123179092A>G

(GRCm39)3:123179710T>C

(Mus musculus)
Allele/Variant
Source: rs48351937
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123179710T>C

(GRCm39)3:123166649A>G

(Mus musculus)
Allele/Variant
Source: rs233050889
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123166649A>G

(GRCm39)3:123163687G>A

(Mus musculus)
Allele/Variant
Source: rs46239116
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123163687G>A

(GRCm39)3:123166661G>A

(Mus musculus)
Allele/Variant
Source: rs52479052
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123166661G>A

(GRCm39)3:123167404T>A

(Mus musculus)
Allele/Variant
Source: rs36457811
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123167404T>A

(GRCm39)3:123167446G>C

(Mus musculus)
Allele/Variant
Source: rs239512951
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123167446G>C

(GRCm39)3:123162421G>C

(Mus musculus)
Allele/Variant
Source: rs36256271
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123162421G>C

(GRCm39)3:123168560G>A

(Mus musculus)
Allele/Variant
Source: rs31331499
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123168560G>A

(GRCm39)3:123167859G>A

(Mus musculus)
Allele/Variant
Source: rs36407553
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123167859G>A

(GRCm39)3:123168831C>T

(Mus musculus)
Allele/Variant
Source: rs219651635
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123168831C>T

(GRCm39)3:123164332G>A

(Mus musculus)
Allele/Variant
Source: rs252963107
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123164332G>A

(GRCm39)3:123164347T>C

(Mus musculus)
Allele/Variant
Source: rs31675828
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123164347T>C

(GRCm39)3:123164440T>C

(Mus musculus)
Allele/Variant
Source: rs220800733
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123164440T>C

(GRCm39)3:123170955C>T

(Mus musculus)
Allele/Variant
Source: rs51471871
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123170955C>T

(GRCm39)3:123171951A>G

(Mus musculus)
Allele/Variant
Source: rs31503307
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123171951A>G

(GRCm39)3:123173203C>T

(Mus musculus)
Allele/Variant
Source: rs30104258
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123173203C>T

(GRCm39)3:123172289T>C

(Mus musculus)
Allele/Variant
Source: rs252962931
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123172289T>C

(GRCm39)3:123177220A>G

(Mus musculus)
Allele/Variant
Source: rs30504253
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123177220A>G

(GRCm39)3:123163022G>C

(Mus musculus)
Allele/Variant
Source: rs246655910
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123163022G>C

(GRCm39)3:123163587T>C

(Mus musculus)
Allele/Variant
Source: rs237938950
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123163587T>C

(GRCm39)3:123166637A>G

(Mus musculus)
Allele/Variant
Source: rs216079511
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123166637A>G

(GRCm39)3:123163759T>C

(Mus musculus)
Allele/Variant
Source: rs36561323
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123163759T>C

(GRCm39)3:123166885G>A

(Mus musculus)
Allele/Variant
Source: rs243122139
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123166885G>A

(GRCm39)3:123162515C>G

(Mus musculus)
Allele/Variant
Source: rs50461830
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123162515C>G

(GRCm39)3:123164859C>T

(Mus musculus)
Allele/Variant
Source: rs252888627
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123164859C>T

(GRCm39)3:123170554A>G

(Mus musculus)
Allele/Variant
Source: rs234764092
Genes: Mettl14 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)3:123170554A>G