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AGACGGTGAAGAGCGTGACGGAGAA[A/G]GCCAGCGTGCCAGTGCGCACCTCGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601901 | ||||||||||||||||||||
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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There are no transcripts associated with this gene. |
SLC8A2 - solute carrier family 8 member A2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015063.2 | 2637 | Silent Mutation | GCC,GCT | A,A 856 | NP_055878.1 | |
XM_005259172.1 | 2637 | Silent Mutation | GCC,GCT | A,A 850 | XP_005259229.1 | |
XM_017027159.1 | 2637 | Silent Mutation | GCC,GCT | A,A 280 | XP_016882648.1 |