Version: 8.0.0
Date: Tue Jan 28 2025
1,032 results for rufy2
Allele/Variant

Rufy2em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7305670
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Rufy2 (Mmu)
Genes: Rufy2 (Mmu)
Symbol: Rufy2em1Gpt

Rufy2tm1a(EUCOMM)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:4434385
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Rufy2 (Mmu)
Genes: Rufy2 (Mmu)
Symbol: Rufy2tm1a(EUCOMM)Wtsi

Rufy2em9Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7305671
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Rufy2 (Mmu)
Genes: Rufy2 (Mmu)
Symbol: Rufy2em9Gpt

la027406Tg

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130129-2233
Genes: rufy2 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: rufy2 (Dre)

Hsap\RUFY2UAS.Tag:HA

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0388519
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Hsap\RUFY2
Construct Expressed Component: RUFY2 (Hsa)

sa6296

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-18141
Genes: rufy2 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: rufy2 (Dre)

(GRCh38)10:68404730T>C

(Homo sapiens)
Allele/Variant
Source: rs772732981
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68404730T>C

(GRCh38)10:68386127T>G

(Homo sapiens)
Allele/Variant
Source: rs996731103
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68386127T>G

(GRCh38)10:68363653T>A

(Homo sapiens)
Allele/Variant
Source: NC_000010.11:g.68363653T>A
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68363653T>A

(GRCh38)10:68406780C>A

(Homo sapiens)
Allele/Variant
Source: rs762065487
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68406780C>A

(GRCh38)10:68396849C>T

(Homo sapiens)
Allele/Variant
Source: rs267602554
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68396849C>T

(GRCh38)10:68401668G>A

(Homo sapiens)
Allele/Variant
Source: NC_000010.11:g.68401668G>A
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68401668G>A

(GRCh38)10:68406766G>A

(Homo sapiens)
Allele/Variant
Source: rs200501110
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68406766G>A

(GRCh38)10:68364090T>G

(Homo sapiens)
Allele/Variant
Source: rs370795568
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68364090T>G

(GRCh38)10:68383874T>C

(Homo sapiens)
Allele/Variant
Source: rs2049280309
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68383874T>C

(GRCh38)10:68379478C>T

(Homo sapiens)
Allele/Variant
Source: rs202078546
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68379478C>T

(GRCh38)10:68383841T>C

(Homo sapiens)
Allele/Variant
Source: rs1044281127
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68383841T>C

(GRCh38)10:68401638C>T

(Homo sapiens)
Allele/Variant
Source: rs774388674
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68401638C>T

(GRCh38)10:68406841A>C

(Homo sapiens)
Allele/Variant
Source: rs769215045
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68406841A>C

(GRCh38)10:68383905C>T

(Homo sapiens)
Allele/Variant
Source: rs371028948
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68383905C>T

(GRCh38)10:68394089A>C

(Homo sapiens)
Allele/Variant
Source: rs770342069
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68394089A>C

(GRCh38)10:68346059T>G

(Homo sapiens)
Allele/Variant
Source: rs369778216
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68346059T>G

(GRCh38)10:68401657C>G

(Homo sapiens)
Allele/Variant
Source: rs752288965
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68401657C>G

(GRCh38)10:68376946A>C

(Homo sapiens)
Allele/Variant
Source: rs758709452
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68376946A>C

(GRCh38)10:68379494T>C

(Homo sapiens)
Allele/Variant
Source: NC_000010.11:g.68379494T>C
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68379494T>C

(GRCh38)10:68341629G>A

(Homo sapiens)
Allele/Variant
Source: rs150055889
Genes: HNRNPH3 (Hsa), RUFY2 (Hsa)
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: (GRCh38)10:68341629G>A

(GRCh38)10:68383812A>G

(Homo sapiens)
Allele/Variant
Source: rs769858718
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68383812A>G

(GRCh38)10:68383859C>T

(Homo sapiens)
Allele/Variant
Source: rs760366895
Genes: RUFY2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:68383859C>T

(mRatBN7.2)20:25635843T>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051355.1:g.25635843T>A
Genes: Rufy2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:25635843T>A

(mRatBN7.2)20:25655812C>T

(Rattus norvegicus)
Allele/Variant
Source: rs104902362
Genes: Rufy2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:25655812C>T

(GRCm39)10:62850214T>C

(Mus musculus)
Allele/Variant
Source: rs223355751
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62850214T>C

(GRCm39)10:62850240C>A

(Mus musculus)
Allele/Variant
Source: rs259854021
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62850240C>A

(GRCm39)10:62849294G>A

(Mus musculus)
Allele/Variant
Source: rs585316346
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62849294G>A

(GRCm39)10:62816026G>C

(Mus musculus)
Allele/Variant
Source: rs212690709
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62816026G>C

(GRCm39)10:62816143G>T

(Mus musculus)
Allele/Variant
Source: rs251033899
Genes: Rufy2 (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)10:62816143G>T

(GRCm39)10:62816388G>C

(Mus musculus)
Allele/Variant
Source: rs223526313
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62816388G>C

(GRCm39)10:62816443G>T

(Mus musculus)
Allele/Variant
Source: rs240653432
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62816443G>T

(GRCm39)10:62816471C>G

(Mus musculus)
Allele/Variant
Source: rs247174679
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62816471C>G

(mRatBN7.2)20:25648983A>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051355.1:g.25648983A>T
Genes: Rufy2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:25648983A>T

(mRatBN7.2)20:25655267G>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051355.1:g.25655267G>T
Genes: Rufy2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:25655267G>T

(mRatBN7.2)20:25648998T>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051355.1:g.25648998T>C
Genes: Rufy2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:25648998T>C

(GRCm39)10:62849427A>C

(Mus musculus)
Allele/Variant
Source: rs229144968
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62849427A>C

(GRCm39)10:62848001G>T

(Mus musculus)
Allele/Variant
Source: rs241212530
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62848001G>T

(GRCm39)10:62847930C>T

(Mus musculus)
Allele/Variant
Source: rs585310949
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62847930C>T

(GRCm39)10:62849390G>A

(Mus musculus)
Allele/Variant
Source: rs260549751
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62849390G>A

(GRCm39)10:62849562G>A

(Mus musculus)
Allele/Variant
Source: rs259945234
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62849562G>A

(GRCm39)10:62850032A>T

(Mus musculus)
Allele/Variant
Source: rs578725454
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62850032A>T

(GRCm39)10:62850041A>T

(Mus musculus)
Allele/Variant
Source: rs586084278
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62850041A>T

(mRatBN7.2)20:25636318G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198345824
Genes: Rufy2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:25636318G>A

(mRatBN7.2)20:25650755C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051355.1:g.25650755C>T
Genes: Rufy2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:25650755C>T