Version: 8.0.0
Date: Tue Jan 28 2025
548 results for pura
Allele/Variant Species: Drosophila melanogaster

Puratm1Kkh

(Mus musculus)
Allele/Variant
Source: MGI:2677937
Genes: Pura (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Pura (Mmu)
Genes: Pura (Mmu)
Symbol: Puratm1Kkh

Puraem1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7305010
Genes: Pura (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Pura (Mmu)
Genes: Pura (Mmu)
Symbol: Puraem1Gpt

Puraem2Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7305011
Genes: Pura (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Pura (Mmu)
Genes: Pura (Mmu)
Symbol: Puraem2Gpt

Puraem1Tht

(Mus musculus)
Allele/Variant
Source: MGI:7546878
Genes: Pura (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Pura (Mmu)
Genes: Pura (Mmu)
Symbol: Puraem1Tht

Puratm1Herm

(Mus musculus)
Allele/Variant
Source: MGI:5305287
Genes: Pura (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Pura (Mmu)
Genes: Pura (Mmu)
Symbol: Puratm1Herm

(GRCh38)5:140114835G>T

(Homo sapiens)
Allele/Variant
Source: rs1040360891
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114835G>T

(GRCh38)5:140114847C>T

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.140114847C>T
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114847C>T

(GRCh38)5:140114907G>C

(Homo sapiens)
Allele/Variant
Source: rs1581036621
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114907G>C

(GRCh38)5:140114766C>G

(Homo sapiens)
Allele/Variant
Source: rs1581036515
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114766C>G

(GRCh38)5:140114778T>C

(Homo sapiens)
Allele/Variant
Source: rs762183564
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114778T>C

(GRCh38)5:140115050C>T

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.140115050C>T
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140115050C>T

(GRCh38)5:140114915G>C

(Homo sapiens)
Allele/Variant
Source: rs1554129118
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114915G>C

(GRCh38)5:140114985A>G

(Homo sapiens)
Allele/Variant
Source: rs1581036671
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114985A>G

(GRCh38)5:140114745T>C

(Homo sapiens)
Allele/Variant
Source: rs1581036495
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114745T>C

(GRCh38)5:140114753C>T

(Homo sapiens)
Allele/Variant
Source: rs1064795165
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114753C>T

(GRCh38)5:140114907G>A

(Homo sapiens)
Allele/Variant
Source: rs1581036621
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114907G>A

(GRCh38)5:140114977A>T

(Homo sapiens)
Allele/Variant
Source: rs1554129129
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)5:140114977A>T

(GRCh38)5:140114983G>T

(Homo sapiens)
Allele/Variant
Source: rs2126749415
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)5:140114983G>T

(GRCh38)5:140114776C>T

(Homo sapiens)
Allele/Variant
Source: rs1763051347
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114776C>T

(GRCh38)5:140114877C>T

(Homo sapiens)
Allele/Variant
Source: rs773542859
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114877C>T

(GRCh38)5:140114784T>C

(Homo sapiens)
Allele/Variant
Source: rs1276094504
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114784T>C

(GRCh38)5:140115048G>C

(Homo sapiens)
Allele/Variant
Source: rs2126749465
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140115048G>C

(GRCh38)5:140114737C>T

(Homo sapiens)
Allele/Variant
Source: rs587782993
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)5:140114737C>T

(GRCh38)5:140114940T>C

(Homo sapiens)
Allele/Variant
Source: rs1581036642
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114940T>C

(GRCh38)5:140114944A>G

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.140114944A>G
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114944A>G

(GRCh38)5:140114724C>T

(Homo sapiens)
Allele/Variant
Source: rs555886273
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114724C>T

(GRCh38)5:140114744T>C

(Homo sapiens)
Allele/Variant
Source: rs793888527
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114744T>C

(GRCh38)5:140114746G>C

(Homo sapiens)
Allele/Variant
Source: rs1581036496
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114746G>C

(GRCh38)5:140114914C>T

(Homo sapiens)
Allele/Variant
Source: rs1554129116
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)5:140114914C>T

(GRCh38)5:140114916A>G

(Homo sapiens)
Allele/Variant
Source: rs1581036630
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114916A>G

(GRCh38)5:140114985A>C

(Homo sapiens)
Allele/Variant
Source: rs1581036671
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114985A>C

(GRCh38)5:140114988C>T

(Homo sapiens)
Allele/Variant
Source: rs760453180
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114988C>T

(GRCh38)5:140115005C>A

(Homo sapiens)
Allele/Variant
Source: rs2126749442
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)5:140115005C>A

(GRCh38)5:140115007G>T

(Homo sapiens)
Allele/Variant
Source: rs2126749445
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)5:140115007G>T

(GRCh38)5:140114754C>G

(Homo sapiens)
Allele/Variant
Source: rs925159576
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114754C>G

(GRCh38)5:140114728A>G

(Homo sapiens)
Allele/Variant
Source: rs1386400193
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114728A>G

(GRCh38)5:140114874C>T

(Homo sapiens)
Allele/Variant
Source: rs750557574
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114874C>T

(GRCh38)5:140114829C>T

(Homo sapiens)
Allele/Variant
Source: rs764016282
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114829C>T

(GRCh38)5:140114950A>G

(Homo sapiens)
Allele/Variant
Source: rs770307150
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114950A>G

(GRCh38)5:140114958G>C

(Homo sapiens)
Allele/Variant
Source: rs146964273
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114958G>C

(GRCh38)5:140114832G>T

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.140114832G>T
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114832G>T

(GRCh38)5:140114855C>T

(Homo sapiens)
Allele/Variant
Source: rs1763053031
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114855C>T

(GRCh38)5:140114873T>G

(Homo sapiens)
Allele/Variant
Source: rs1554129113
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114873T>G

(GRCh38)5:140114974G>A

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.140114974G>A
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114974G>A

(GRCh38)5:140115000G>A

(Homo sapiens)
Allele/Variant
Source: NC_000005.10:g.140115000G>A
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140115000G>A

(GRCh38)5:140114819A>T

(Homo sapiens)
Allele/Variant
Source: rs1763052435
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114819A>T

(GRCh38)5:140114866A>T

(Homo sapiens)
Allele/Variant
Source: rs1057524637
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)5:140114866A>T

(GRCh38)5:140114883T>C

(Homo sapiens)
Allele/Variant
Source: rs1581036605
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114883T>C

(GRCh38)5:140114901C>T

(Homo sapiens)
Allele/Variant
Source: rs1763053854
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114901C>T

(GRCh38)5:140114763G>T

(Homo sapiens)
Allele/Variant
Source: rs886603107
Genes: PURA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:140114763G>T