Version: 8.0.0
Date: Tue Jan 28 2025
51 results for rufy2
Allele/Variant Molecular Consequence: intron 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)10:68363653T>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)10:68401668G>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)10:68364090T>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)10:68383905C>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)10:68383812A>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

(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)10:62818550G>A

(Mus musculus)
Allele/Variant
Source: rs229459477
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62818550G>A

(GRCm39)10:62828911C>T

(Mus musculus)
Allele/Variant
Source: rs228198651
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62828911C>T

(GRCm39)10:62845180A>C

(Mus musculus)
Allele/Variant
Source: rs234708492
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62845180A>C

(GRCm39)10:62847546G>A

(Mus musculus)
Allele/Variant
Source: rs220401975
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62847546G>A

(GRCm39)10:62816107C>T

(Mus musculus)
Allele/Variant
Source: rs245833693
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)10:62816107C>T

(GRCm39)10:62828971C>T

(Mus musculus)
Allele/Variant
Source: rs228718434
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62828971C>T

(GRCm39)10:62818572C>T

(Mus musculus)
Allele/Variant
Source: rs231925786
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62818572C>T

(GRCm39)10:62830496C>T

(Mus musculus)
Allele/Variant
Source: rs263900970
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62830496C>T

(GRCm39)10:62816072C>G

(Mus musculus)
Allele/Variant
Source: rs229348680
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)10:62816072C>G

(GRCm39)10:62824990G>A

(Mus musculus)
Allele/Variant
Source: rs247463301
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62824990G>A

(GRCm39)10:62833905C>T

(Mus musculus)
Allele/Variant
Source: rs249296975
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62833905C>T

(GRCm39)10:62842503T>C

(Mus musculus)
Allele/Variant
Source: rs240054697
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62842503T>C

(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)20:25647911G>T

(Rattus norvegicus)
Allele/Variant
Source: rs197182428
Genes: Rufy2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:25647911G>T

(GRCm39)10:62815974A>G

(Mus musculus)
Allele/Variant
Source: rs226063423
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)10:62815974A>G

(GRCm39)10:62833920C>T

(Mus musculus)
Allele/Variant
Source: rs212947365
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62833920C>T

(GRCm39)10:62830499C>T

(Mus musculus)
Allele/Variant
Source: rs234740187
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62830499C>T

(GRCm39)10:62828966T>C

(Mus musculus)
Allele/Variant
Source: rs49652590
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62828966T>C

(GRCm39)10:62833729C>A

(Mus musculus)
Allele/Variant
Source: rs47252805
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62833729C>A

(GRCm39)10:62818469C>T

(Mus musculus)
Allele/Variant
Source: rs240436127
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62818469C>T

(GRCm39)10:62847610C>T

(Mus musculus)
Allele/Variant
Source: rs29351626
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62847610C>T

(GRCm39)10:62815948G>A

(Mus musculus)
Allele/Variant
Source: rs260148225
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)10:62815948G>A

(GRCm39)10:62847540C>G

(Mus musculus)
Allele/Variant
Source: rs258066501
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62847540C>G

(GRCm39)10:62818460C>T

(Mus musculus)
Allele/Variant
Source: rs221063051
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62818460C>T

(GRCm39)10:62816077C>A

(Mus musculus)
Allele/Variant
Source: rs253514914
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)10:62816077C>A

(GRCm39)10:62818529T>C

(Mus musculus)
Allele/Variant
Source: rs257703205
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62818529T>C

(GRCm39)10:62816020C>T

(Mus musculus)
Allele/Variant
Source: rs251818201
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)10:62816020C>T

(GRCm39)10:62828954C>T

(Mus musculus)
Allele/Variant
Source: rs247299778
Genes: Rufy2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:62828954C>T