Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAAGATCCCCCTCTTCTTGTTTCGC[C/T]GTCGCTCCTGGTCCAAGTCCTCATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
MEIS3 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
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 |
MEIS3 - Meis homeobox 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001009813.2 | 1427 | Intron | NP_001009813.1 | |||
NM_001301059.1 | 1427 | Intron | NP_001287988.1 | |||
NM_020160.2 | 1427 | Intron | NP_064545.1 | |||
XM_011527136.2 | 1427 | Missense Mutation | CAG,CGG | Q,R 332 | XP_011525438.1 | |
XM_011527138.2 | 1427 | Missense Mutation | CAG,CGG | Q,R 282 | XP_011525440.1 | |
XM_011527139.2 | 1427 | Intron | XP_011525441.1 | |||
XM_011527140.1 | 1427 | Missense Mutation | CAG,CGG | Q,R 129 | XP_011525442.1 | |
XM_017027011.1 | 1427 | Missense Mutation | CAG,CGG | Q,R 349 | XP_016882500.1 |