Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant Molecular Consequence: intron variant
(GRCh38)1:246557447G>A
(Homo sapiens)Allele/Variant
Source: rs1422493014
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246557447G>A
(GRCh38)1:246557457T>C
(Homo sapiens)Allele/Variant
Source: rs112020559
Genes: TFB2M (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:246557457T>C
(mRatBN7.2)13:91289949G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91289949G>A
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91289949G>A
(mRatBN7.2)13:91283812G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91283812G>A
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91283812G>A
(mRatBN7.2)13:91294797T>C
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91294797T>C
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91294797T>C
(mRatBN7.2)13:91280084G>C
(Rattus norvegicus)Allele/Variant
Source: rs3322315793
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91280084G>C
(mRatBN7.2)13:91282120T>C
(Rattus norvegicus)Allele/Variant
Source: rs3322433281
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91282120T>C
(mRatBN7.2)13:91290309G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91290309G>A
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91290309G>A
(mRatBN7.2)13:91286850T>C
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91286850T>C
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91286850T>C
(mRatBN7.2)13:91279954A>G
(Rattus norvegicus)Allele/Variant
Source: rs3322337541
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91279954A>G
(mRatBN7.2)13:91293831G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91293831G>A
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91293831G>A
(mRatBN7.2)13:91295012C>T
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91295012C>T
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91295012C>T
(mRatBN7.2)13:91284958A>G
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91284958A>G
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91284958A>G
(mRatBN7.2)13:91294504C>T
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91294504C>T
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91294504C>T
(mRatBN7.2)13:91281089T>A
(Rattus norvegicus)Allele/Variant
Source: rs3322485070
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91281089T>A
(mRatBN7.2)13:91283695T>A
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91283695T>A
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91283695T>A
(mRatBN7.2)13:91284400A>T
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91284400A>T
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91284400A>T
(mRatBN7.2)13:91286062T>G
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91286062T>G
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91286062T>G
(mRatBN7.2)13:91288992G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91288992G>A
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91288992G>A
(mRatBN7.2)13:91288366G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91288366G>A
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91288366G>A
(mRatBN7.2)13:91284568T>C
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91284568T>C
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91284568T>C
(mRatBN7.2)13:91287433A>G
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91287433A>G
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91287433A>G
(mRatBN7.2)13:91292229C>A
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91292229C>A
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91292229C>A
(mRatBN7.2)13:91292446G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91292446G>A
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91292446G>A
(mRatBN7.2)13:91280404C>G
(Rattus norvegicus)Allele/Variant
Source: rs3322433276
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91280404C>G
(mRatBN7.2)13:91282514T>C
(Rattus norvegicus)Allele/Variant
Source: rs3322315645
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91282514T>C
(mRatBN7.2)13:91285678A>G
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91285678A>G
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91285678A>G
(mRatBN7.2)13:91290081C>T
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91290081C>T
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91290081C>T
(mRatBN7.2)13:91287044C>A
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91287044C>A
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91287044C>A
(mRatBN7.2)13:91280578G>T
(Rattus norvegicus)Allele/Variant
Source: rs3322277391
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91280578G>T
(mRatBN7.2)13:91282625G>C
(Rattus norvegicus)Allele/Variant
Source: rs3322277408
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91282625G>C
(mRatBN7.2)13:91283196G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91283196G>A
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91283196G>A
(mRatBN7.2)13:91281412T>C
(Rattus norvegicus)Allele/Variant
Source: rs3322529580
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91281412T>C
(mRatBN7.2)13:91283276A>G
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91283276A>G
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91283276A>G
(mRatBN7.2)13:91283541C>T
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91283541C>T
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91283541C>T
(mRatBN7.2)13:91292919C>G
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91292919C>G
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91292919C>G
(mRatBN7.2)13:91295143C>G
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91295143C>G
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91295143C>G
(mRatBN7.2)13:91284552A>G
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91284552A>G
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91284552A>G
(mRatBN7.2)13:91288675G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91288675G>A
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91288675G>A
(mRatBN7.2)13:91291404C>T
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91291404C>T
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91291404C>T
(mRatBN7.2)13:91284780A>G
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91284780A>G
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91284780A>G
(mRatBN7.2)13:91285198T>C
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91285198T>C
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91285198T>C
(mRatBN7.2)13:91283408T>C
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91283408T>C
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91283408T>C
(mRatBN7.2)13:91292364T>A
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91292364T>A
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91292364T>A
(mRatBN7.2)13:91286103G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91286103G>A
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91286103G>A
(mRatBN7.2)13:91294294C>A
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91294294C>A
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91294294C>A
(mRatBN7.2)13:91285873G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051348.1:g.91285873G>A
Genes: Tfb2m (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:91285873G>A
(GRCm39)1:179359715G>A
(Mus musculus)Allele/Variant
Source: rs237293238
Genes: Tfb2m (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:179359715G>A
(GRCm39)1:179357758T>C
(Mus musculus)Allele/Variant
Source: rs584877843
Genes: Tfb2m (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:179357758T>C
(GRCm39)1:179363035A>G
(Mus musculus)Allele/Variant
Source: rs258880798
Genes: Tfb2m (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:179363035A>G