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CCCAGTGAAGCGCTCTGAGAAGGCC[A/G]TGGATGCCCCACCAGCGTCCCAGAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C7orf57 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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C7orf57 - chromosome 7 open reading frame 57 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001100159.2 | 162 | Missense Mutation | ATG,GTG | M,V 33 | NP_001093629.1 | |
NM_001267865.1 | 162 | UTR 5 | NP_001254794.1 | |||
NM_001267866.1 | 162 | UTR 5 | NP_001254795.1 | |||
XM_006715649.3 | 162 | Missense Mutation | ATG,GTG | M,V 33 | XP_006715712.1 | |
XM_006715650.2 | 162 | UTR 5 | XP_006715713.1 | |||
XM_011515121.1 | 162 | Missense Mutation | ATG,GTG | M,V 33 | XP_011513423.1 | |
XM_011515122.2 | 162 | Missense Mutation | ATG,GTG | M,V 33 | XP_011513424.1 | |
XM_011515123.2 | 162 | Missense Mutation | ATG,GTG | M,V 33 | XP_011513425.1 |
SUN3 - Sad1 and UNC84 domain containing 3 | ||||||
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There are no transcripts associated with this gene. |