Version: 8.0.0
Date: Tue Jan 28 2025
651 results for tfb2m
Allele/Variant

Tfb2mtm1a(KOMP)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:4363126
Genes: Tfb2m (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Tfb2m (Mmu)
Genes: Tfb2m (Mmu)
Symbol: Tfb2mtm1a(KOMP)Wtsi

Tfb2mem1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7307343
Genes: Tfb2m (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Tfb2m (Mmu)
Genes: Tfb2m (Mmu)
Symbol: Tfb2mem1Gpt

Tfb2mem1Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7292735
Genes: Tfb2m (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Tfb2m (Mmu)
Genes: Tfb2m (Mmu)
Symbol: Tfb2mem1Smoc

(R6)3R:10045830G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033777.3:g.10045830G>A
Genes: mtTFB2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)3R:10045830G>A
Gene Synonyms: TFB2M

(R6)3R:10047078C>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033777.3:g.10047078C>A
Genes: mtTFB2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:10047078C>A
Gene Synonyms: TFB2M

(R6)3R:10045822G>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033777.3:g.10045822G>T
Genes: mtTFB2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:10045822G>T
Gene Synonyms: TFB2M

sa36345

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-4555
Genes: tfb2m (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: tfb2m (Dre)

(R6)3R:10045584G>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033777.3:g.10045584G>T
Genes: mtTFB2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)3R:10045584G>T
Gene Synonyms: TFB2M

(R6)3R:10045994A>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033777.3:g.10045994A>G
Genes: mtTFB2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:10045994A>G
Gene Synonyms: TFB2M

(R6)3R:10047166C>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033777.3:g.10047166C>A
Genes: mtTFB2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)3R:10047166C>A
Gene Synonyms: TFB2M

(R6)3R:10045752T>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033777.3:g.10045752T>G
Genes: mtTFB2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:10045752T>G
Gene Synonyms: TFB2M

(R6)3R:10046962C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033777.3:g.10046962C>T
Genes: mtTFB2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)3R:10046962C>T
Gene Synonyms: TFB2M

(R6)3R:10046841C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033777.3:g.10046841C>T
Genes: mtTFB2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:10046841C>T
Gene Synonyms: TFB2M

(R6)3R:10046611C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033777.3:g.10046611C>T
Genes: mtTFB2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:10046611C>T
Gene Synonyms: TFB2M

(R6)3R:10045590G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033777.3:g.10045590G>A
Genes: mtTFB2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)3R:10045590G>A
Gene Synonyms: TFB2M

(R6)3R:10046977G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033777.3:g.10046977G>A
Genes: mtTFB2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)3R:10046977G>A
Gene Synonyms: TFB2M

(R6)3R:10045941G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033777.3:g.10045941G>A
Genes: mtTFB2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)3R:10045941G>A
Gene Synonyms: TFB2M

(R6)3R:10045923G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033777.3:g.10045923G>A
Genes: mtTFB2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)3R:10045923G>A
Gene Synonyms: TFB2M

(R6)3R:10045814C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033777.3:g.10045814C>T
Genes: mtTFB2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:10045814C>T
Gene Synonyms: TFB2M

(R6)3R:10045719C>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033777.3:g.10045719C>G
Genes: mtTFB2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)3R:10045719C>G
Gene Synonyms: TFB2M

(R6)3R:10046116G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033777.3:g.10046116G>A
Genes: mtTFB2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:10046116G>A
Gene Synonyms: TFB2M

(R6)3R:10047183G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033777.3:g.10047183G>A
Genes: mtTFB2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:10047183G>A
Gene Synonyms: TFB2M

(R6)3R:10045958T>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033777.3:g.10045958T>A
Genes: mtTFB2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)3R:10045958T>A
Gene Synonyms: TFB2M

sa2933

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-13736
Genes: tfb2m (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: tfb2m (Dre)

sa10078

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130411-70
Genes: tfb2m (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: tfb2m (Dre)

(GRCh38)1:246548573T>G

(Homo sapiens)
Allele/Variant
Source: rs367762353
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246548573T>G

(GRCh38)1:246544522G>A

(Homo sapiens)
Allele/Variant
Source: rs778528523
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246544522G>A

(GRCh38)1:246544540T>C

(Homo sapiens)
Allele/Variant
Source: rs768249338
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246544540T>C

(GRCh38)1:246564370G>A

(Homo sapiens)
Allele/Variant
Source: rs34587495
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246564370G>A

(GRCh38)1:246565952T>C

(Homo sapiens)
Allele/Variant
Source: rs747062180
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246565952T>C

(GRCh38)1:246565996G>A

(Homo sapiens)
Allele/Variant
Source: rs148620105
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246565996G>A

(GRCh38)1:246544534T>C

(Homo sapiens)
Allele/Variant
Source: rs779474412
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246544534T>C

(GRCh38)1:246548576C>T

(Homo sapiens)
Allele/Variant
Source: rs545105645
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246548576C>T

(GRCh38)1:246564414C>T

(Homo sapiens)
Allele/Variant
Source: rs772156827
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246564414C>T

(GRCh38)1:246565886C>A

(Homo sapiens)
Allele/Variant
Source: rs1659649295
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246565886C>A

(GRCh38)1:246541046G>A

(Homo sapiens)
Allele/Variant
Source: rs143882766
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246541046G>A

(GRCh38)1:246541065T>C

(Homo sapiens)
Allele/Variant
Source: rs781540747
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246541065T>C

(GRCh38)1:246566114G>A

(Homo sapiens)
Allele/Variant
Source: rs1659663391
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246566114G>A

(GRCh38)1:246541087G>A

(Homo sapiens)
Allele/Variant
Source: rs767077089
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246541087G>A

(GRCh38)1:246544548C>T

(Homo sapiens)
Allele/Variant
Source: rs770122933
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246544548C>T

(GRCh38)1:246548579G>T

(Homo sapiens)
Allele/Variant
Source: rs767272722
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246548579G>T

(GRCh38)1:246551284C>T

(Homo sapiens)
Allele/Variant
Source: rs776235911
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246551284C>T

(GRCh38)1:246566072A>C

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.246566072A>C
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246566072A>C

(GRCh38)1:246566081C>T

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.246566081C>T
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246566081C>T

(GRCh38)1:246544662T>G

(Homo sapiens)
Allele/Variant
Source: rs966820999
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246544662T>G

(GRCh38)1:246565918T>A

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.246565918T>A
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246565918T>A

(GRCh38)1:246541061C>T

(Homo sapiens)
Allele/Variant
Source: rs747987612
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)1:246541061C>T

(GRCh38)1:246541172T>C

(Homo sapiens)
Allele/Variant
Source: rs200741232
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246541172T>C

(GRCh38)1:246557447G>A

(Homo sapiens)
Allele/Variant
Source: rs1422493014
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246557447G>A

(GRCh38)1:246565910C>A

(Homo sapiens)
Allele/Variant
Source: rs1659650645
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246565910C>A