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GCCTCTTTAACCTGTAATGCTGTGG[C/G]TAGCCCTTGGCCCCTTTCCTGCCAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602520 | ||||||||||||||||||||
Literature Links: |
MAP2K5 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 |
MAP2K5 - mitogen-activated protein kinase kinase 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001206804.1 | 740 | Intron | NP_001193733.1 | |||
NM_002757.3 | 740 | Missense Mutation | CTA,GTA | L,V 4 | NP_002748.1 | |
NM_145160.2 | 740 | Missense Mutation | CTA,GTA | L,V 4 | NP_660143.1 | |
XM_011521787.2 | 740 | Missense Mutation | CTA,GTA | L,V 4 | XP_011520089.1 | |
XM_011521788.2 | 740 | Missense Mutation | CTA,GTA | L,V 4 | XP_011520090.1 | |
XM_017022414.1 | 740 | Missense Mutation | CTA,GTA | L,V 4 | XP_016877903.1 |