Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGGCCCTCTGGGCTGAAGGCTGCA[A/C]CCTGCCCTGCGAAGGGGGTTCAGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||||||||||||||||||||
Literature Links: |
MEIS3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
MEIS3 - Meis homeobox 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001009813.2 | 1646 | Intron | NP_001009813.1 | |||
NM_001301059.1 | 1646 | Intron | NP_001287988.1 | |||
NM_020160.2 | 1646 | Intron | NP_064545.1 | |||
XM_011527136.2 | 1646 | Missense Mutation | GGT,GTT | G,V 405 | XP_011525438.1 | |
XM_011527138.2 | 1646 | Missense Mutation | GGT,GTT | G,V 355 | XP_011525440.1 | |
XM_011527139.2 | 1646 | Intron | XP_011525441.1 | |||
XM_011527140.1 | 1646 | Missense Mutation | GGT,GTT | G,V 202 | XP_011525442.1 | |
XM_017027011.1 | 1646 | Missense Mutation | GGT,GTT | G,V 422 | XP_016882500.1 |