Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
Ctrb1Gt(OST27792)Lex
(Mus musculus)Allele/Variant
Source: MGI:3529453
Genes: Ctrb1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ctrb1
Genes: Ctrb1 (Mmu)
Symbol: Ctrb1Gt(OST27792)Lex
Ctrb1em1Toth
(Mus musculus)Allele/Variant
Source: MGI:6455002
Genes: Ctrb1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ctrb1
Genes: Ctrb1 (Mmu)
Symbol: Ctrb1em1Toth
Ctrb1em1Smoc
(Mus musculus)Allele/Variant
Source: MGI:7289193
Genes: Ctrb1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ctrb1
Genes: Ctrb1 (Mmu)
Symbol: Ctrb1em1Smoc
zf3439Tg
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-220520-2
Genes: ctrb.1 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: ctrb1
sa21002
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-160601-124
Genes: ctrb.1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: ctrb1
(GRCh38)16:75224144G>A
(Homo sapiens)Allele/Variant
Source: rs1379132184
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224144G>A
(GRCh38)16:75223010C>T
(Homo sapiens)Allele/Variant
Source: rs988924329
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75223010C>T
(GRCh38)16:75223544G>A
(Homo sapiens)Allele/Variant
Source: rs749947761
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75223544G>A
(GRCh38)16:75222788C>A
(Homo sapiens)Allele/Variant
Source: rs369201413
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75222788C>A
(GRCh38)16:75224162G>A
(Homo sapiens)Allele/Variant
Source: rs772939808
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224162G>A
(GRCh38)16:75224717G>A
(Homo sapiens)Allele/Variant
Source: rs375112297
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224717G>A
(GRCh38)16:75225312C>G
(Homo sapiens)Allele/Variant
Source: rs207476166
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75225312C>G
(GRCh38)16:75219026C>T
(Homo sapiens)Allele/Variant
Source: NC_000016.10:g.75219026C>T
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75219026C>T
(GRCh38)16:75222813G>A
(Homo sapiens)Allele/Variant
Source: rs1460273237
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75222813G>A
(GRCh38)16:75222836G>A
(Homo sapiens)Allele/Variant
Source: rs575650101
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75222836G>A
(GRCh38)16:75222837T>C
(Homo sapiens)Allele/Variant
Source: rs760725877
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75222837T>C
(GRCh38)16:75223041G>A
(Homo sapiens)Allele/Variant
Source: rs1395895685
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75223041G>A
(GRCh38)16:75223215C>A
(Homo sapiens)Allele/Variant
Source: rs2076707794
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75223215C>A
(GRCh38)16:75224088C>T
(Homo sapiens)Allele/Variant
Source: rs922977869
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224088C>T
(GRCh38)16:75224136G>A
(Homo sapiens)Allele/Variant
Source: rs1468304725
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224136G>A
(GRCh38)16:75224148T>C
(Homo sapiens)Allele/Variant
Source: rs1941683318
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224148T>C
(GRCh38)16:75224711T>C
(Homo sapiens)Allele/Variant
Source: rs755026878
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224711T>C
(GRCh38)16:75223580G>T
(Homo sapiens)Allele/Variant
Source: rs1328058568
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75223580G>T
(GRCh38)16:75224124C>T
(Homo sapiens)Allele/Variant
Source: rs749729391
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224124C>T
(GRCh38)16:75224707C>T
(Homo sapiens)Allele/Variant
Source: rs193920783
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224707C>T
(GRCh38)16:75223193A>G
(Homo sapiens)Allele/Variant
Source: NC_000016.10:g.75223193A>G
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75223193A>G
(GRCh38)16:75223565G>A
(Homo sapiens)Allele/Variant
Source: rs778536899
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75223565G>A
(GRCh38)16:75224780G>A
(Homo sapiens)Allele/Variant
Source: rs187077796
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224780G>A
(GRCh38)16:75224816C>T
(Homo sapiens)Allele/Variant
Source: rs146246357
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224816C>T
(GRCh38)16:75224847A>C
(Homo sapiens)Allele/Variant
Source: rs1661070146
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224847A>C
(GRCh38)16:75222803G>A
(Homo sapiens)Allele/Variant
Source: rs372716369
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75222803G>A
(GRCh38)16:75222978G>A
(Homo sapiens)Allele/Variant
Source: rs533494856
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75222978G>A
(GRCh38)16:75224796C>T
(Homo sapiens)Allele/Variant
Source: NC_000016.10:g.75224796C>T
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75224796C>T
(GRCh38)16:75223157G>A
(Homo sapiens)Allele/Variant
Source: rs1475879220
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75223157G>A
(GRCh38)16:75223580G>A
(Homo sapiens)Allele/Variant
Source: rs1328058568
Genes: CTRB1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:75223580G>A
(mRatBN7.2)19:39654863G>C
(Rattus norvegicus)Allele/Variant
Source: rs106456305
Genes: Ctrb1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:39654863G>C
(mRatBN7.2)19:39655318A>C
(Rattus norvegicus)Allele/Variant
Source: rs106427557
Genes: Ctrb1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:39655318A>C
(mRatBN7.2)19:39656181C>A
(Rattus norvegicus)Allele/Variant
Source: rs107027901
Genes: Ctrb1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:39656181C>A
(mRatBN7.2)19:39653937T>G
(Rattus norvegicus)Allele/Variant
Source: rs105182871
Genes: Ctrb1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:39653937T>G
(mRatBN7.2)19:39653993A>T
(Rattus norvegicus)Allele/Variant
Source: rs3323437727
Genes: Ctrb1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:39653993A>T
(mRatBN7.2)19:39656921A>C
(Rattus norvegicus)Allele/Variant
Source: rs105800789
Genes: Ctrb1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:39656921A>C
(mRatBN7.2)19:39654408T>C
(Rattus norvegicus)Allele/Variant
Source: rs105090827
Genes: Ctrb1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:39654408T>C
(mRatBN7.2)19:39655526C>T
(Rattus norvegicus)Allele/Variant
Source: rs3323432958
Genes: Ctrb1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:39655526C>T
(mRatBN7.2)19:39655872A>G
(Rattus norvegicus)Allele/Variant
Source: rs3323383682
Genes: Ctrb1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:39655872A>G
(GRCm39)8:112413566G>C
(Mus musculus)Allele/Variant
Source: rs244199178
Genes: Ctrb1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112413566G>C
(mRatBN7.2)19:39657045G>C
(Rattus norvegicus)Allele/Variant
Source: NC_051354.1:g.39657045G>C
Genes: Ctrb1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:39657045G>C
(mRatBN7.2)19:39657648G>C
(Rattus norvegicus)Allele/Variant
Source: rs199165615
Genes: Ctrb1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:39657648G>C
(mRatBN7.2)19:39652967G>T
(Rattus norvegicus)Allele/Variant
Source: rs3323463485
Genes: Ctrb1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:39652967G>T
(mRatBN7.2)19:39654176A>G
(Rattus norvegicus)Allele/Variant
Source: NC_051354.1:g.39654176A>G
Genes: Ctrb1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:39654176A>G
(mRatBN7.2)19:39654798C>G
(Rattus norvegicus)Allele/Variant
Source: rs105165355
Genes: Ctrb1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)19:39654798C>G