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ATTTATGTTTTTCAGACAGCATAAA[A/C]TAGAGGATGCTGCTATAACATATGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
C2orf73 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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C2orf73 - chromosome 2 open reading frame 73 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001100396.1 | 149 | Missense Mutation | ATA,CTA | I,L 13 | NP_001093866.1 | |
XM_005264133.1 | 149 | Intron | XP_005264190.1 | |||
XM_005264134.3 | 149 | Intron | XP_005264191.1 | |||
XM_011532510.2 | 149 | Missense Mutation | ATA,CTA | I,L 13 | XP_011530812.1 | |
XM_011532513.2 | 149 | Intron | XP_011530815.1 | |||
XM_017003323.1 | 149 | Missense Mutation | ATA,CTA | I,L 13 | XP_016858812.1 | |
XM_017003324.1 | 149 | Missense Mutation | ATA,CTA | I,L 13 | XP_016858813.1 |