Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTCGGCCTCGGCCGCCTCGGCCTCT[C/T]GGCTCACTATGCGCACCTTCTGCCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603166 MIM: 613733 | ||||||||||||||||||||
Literature Links: |
MAP4K2 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 |
MAP4K2 - mitogen-activated protein kinase kinase kinase kinase 2 | ||||||
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There are no transcripts associated with this gene. |
MEN1 - menin 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000244.3 | 1871 | Missense Mutation | CAA,CGA | Q,R 465 | NP_000235.2 | |
NM_130799.2 | 1871 | Missense Mutation | CAA,CGA | Q,R 460 | NP_570711.1 | |
NM_130800.2 | 1871 | Missense Mutation | CAA,CGA | Q,R 465 | NP_570712.1 | |
NM_130801.2 | 1871 | Missense Mutation | CAA,CGA | Q,R 465 | NP_570713.1 | |
NM_130802.2 | 1871 | Missense Mutation | CAA,CGA | Q,R 465 | NP_570714.1 | |
NM_130803.2 | 1871 | Missense Mutation | CAA,CGA | Q,R 465 | NP_570715.1 | |
NM_130804.2 | 1871 | Missense Mutation | CAA,CGA | Q,R 465 | NP_570716.1 | |
XM_005274001.4 | 1871 | Missense Mutation | CAA,CGA | Q,R 460 | XP_005274058.1 | |
XM_011545040.1 | 1871 | Missense Mutation | CAA,CGA | Q,R 502 | XP_011543342.1 | |
XM_011545041.2 | 1871 | Missense Mutation | CAA,CGA | Q,R 502 | XP_011543343.1 | |
XM_011545042.2 | 1871 | Missense Mutation | CAA,CGA | Q,R 502 | XP_011543344.1 | |
XM_017017765.1 | 1871 | Missense Mutation | CAA,CGA | Q,R 507 | XP_016873254.1 | |
XM_017017766.1 | 1871 | Missense Mutation | CAA,CGA | Q,R 507 | XP_016873255.1 | |
XM_017017767.1 | 1871 | Missense Mutation | CAA,CGA | Q,R 507 | XP_016873256.1 | |
XM_017017768.1 | 1871 | Missense Mutation | CAA,CGA | Q,R 507 | XP_016873257.1 | |
XM_017017769.1 | 1871 | Missense Mutation | CAA,CGA | Q,R 460 | XP_016873258.1 | |
XM_017017770.1 | 1871 | Missense Mutation | CAA,CGA | Q,R 460 | XP_016873259.1 |