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CCAAAATGACTACCTGTGAATTCTC[C/T]TGTGTTTAACAAGGATAGACAAGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605422 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZNF350 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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ZNF350 - zinc finger protein 350 | ||||||
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There are no transcripts associated with this gene. |
ZNF615 - zinc finger protein 615 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199324.1 | 2530 | Missense Mutation | AAG,AGG | K,R 738 | NP_001186253.1 | |
NM_001321317.1 | 2530 | Missense Mutation | AAG,AGG | K,R 732 | NP_001308246.1 | |
NM_001321318.1 | 2530 | Missense Mutation | AAG,AGG | K,R 734 | NP_001308247.1 | |
NM_001321319.1 | 2530 | Missense Mutation | AAG,AGG | K,R 738 | NP_001308248.1 | |
NM_001321320.1 | 2530 | Missense Mutation | AAG,AGG | K,R 727 | NP_001308249.1 | |
NM_001321321.1 | 2530 | Missense Mutation | AAG,AGG | K,R 738 | NP_001308250.1 | |
NM_001321322.1 | 2530 | Missense Mutation | AAG,AGG | K,R 734 | NP_001308251.1 | |
NM_001321323.1 | 2530 | Missense Mutation | AAG,AGG | K,R 743 | NP_001308252.1 | |
NM_198480.3 | 2530 | Missense Mutation | AAG,AGG | K,R 727 | NP_940882.3 | |
XM_011526824.1 | 2530 | Missense Mutation | AAG,AGG | K,R 738 | XP_011525126.1 | |
XM_011526825.1 | 2530 | Missense Mutation | AAG,AGG | K,R 738 | XP_011525127.1 | |
XM_011526826.1 | 2530 | Missense Mutation | AAG,AGG | K,R 738 | XP_011525128.1 | |
XM_011526829.1 | 2530 | Missense Mutation | AAG,AGG | K,R 619 | XP_011525131.1 | |
XM_011526830.1 | 2530 | Missense Mutation | AAG,AGG | K,R 619 | XP_011525132.1 | |
XM_017026648.1 | 2530 | Missense Mutation | AAG,AGG | K,R 727 | XP_016882137.1 | |
XM_017026649.1 | 2530 | Missense Mutation | AAG,AGG | K,R 727 | XP_016882138.1 | |
XM_017026650.1 | 2530 | Missense Mutation | AAG,AGG | K,R 619 | XP_016882139.1 | |
XM_017026651.1 | 2530 | Missense Mutation | AAG,AGG | K,R 619 | XP_016882140.1 |
Set Membership: |
HapMap |