Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATGACAGTCGTATTCTGGCAAAATT[C/G]ACAAATAAAGCCCTTTCCTTGACAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
KIAA0226L PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
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Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
KIAA0226L - KIAA0226 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286761.1 | 1761 | Missense Mutation | CAA,GAA | Q,E 605 | NP_001273690.1 | |
NM_001286762.1 | 1761 | Silent Mutation | GTC,GTG | V,V 553 | NP_001273691.1 | |
NM_001286763.1 | 1761 | Missense Mutation | CAA,GAA | Q,E 538 | NP_001273692.1 | |
NM_001286764.1 | 1761 | Missense Mutation | CAA,GAA | Q,E 470 | NP_001273693.1 | |
NM_001286765.1 | 1761 | Missense Mutation | CAA,GAA | Q,E 448 | NP_001273694.1 | |
NM_001286766.1 | 1761 | Missense Mutation | CAA,GAA | Q,E 390 | NP_001273695.1 | |
NM_025113.3 | 1761 | Missense Mutation | CAA,GAA | Q,E 605 | NP_079389.2 |