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AAGCAATGCAATATCCCAAGGTTCC[C/T]GTCTGGGGCAAAAATTCATTAATCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C4orf36 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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C4orf36 - chromosome 4 open reading frame 36 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_144645.3 | 268 | Missense Mutation | CAG,CGG | Q,R 23 | NP_653246.1 | |
XM_011531610.2 | 268 | Missense Mutation | CAG,CGG | Q,R 23 | XP_011529912.1 | |
XM_011531611.2 | 268 | Missense Mutation | CAG,CGG | Q,R 23 | XP_011529913.1 | |
XM_011531612.2 | 268 | Missense Mutation | CAG,CGG | Q,R 23 | XP_011529914.1 | |
XM_011531613.2 | 268 | Intron | XP_011529915.1 | |||
XM_011531615.2 | 268 | Missense Mutation | CAG,CGG | Q,R 23 | XP_011529917.1 | |
XM_017007746.1 | 268 | Missense Mutation | CAG,CGG | Q,R 23 | XP_016863235.1 |