Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCGGACTCAGCTTCTTTGAGGATAC[C/T]TTCCAGTTGGGCAAGTTCCTCTGAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607520 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FRYL 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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FRYL - FRY like transcription coactivator | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015030.1 | 5925 | Missense Mutation | AGT,GGT | S,G 2877 | NP_055845.1 | |
XM_005248090.4 | 5925 | Missense Mutation | AGT,GGT | S,G 2892 | XP_005248147.1 | |
XM_005248093.4 | 5925 | Missense Mutation | AGT,GGT | S,G 1908 | XP_005248150.1 | |
XM_011513680.2 | 5925 | Missense Mutation | AGT,GGT | S,G 2891 | XP_011511982.1 | |
XM_011513681.2 | 5925 | Missense Mutation | AGT,GGT | S,G 2886 | XP_011511983.1 | |
XM_011513682.2 | 5925 | Missense Mutation | AGT,GGT | S,G 2871 | XP_011511984.1 | |
XM_011513683.2 | 5925 | Missense Mutation | AGT,GGT | S,G 2892 | XP_011511985.1 | |
XM_011513684.2 | 5925 | Missense Mutation | AGT,GGT | S,G 1908 | XP_011511986.1 | |
XM_011513685.2 | 5925 | Intron | XP_011511987.1 | |||
XM_017008046.1 | 5925 | Missense Mutation | AGT,GGT | S,G 2877 | XP_016863535.1 |
ZAR1 - zygote arrest 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_175619.2 | 5925 | Intron | NP_783318.1 |