Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGGACTCCTTGTCAGACAGTGACA[G/T]CATCATAGCATATGCCTGGGGTAAA
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 165215 | |||||||||||||||||||||||
Literature Links: |
MECOM PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
MECOM - MDS1 and EVI1 complex locus | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001105077.3 | 3302 | Missense Mutation | ATG,CTG | M,L 1078 | NP_001098547.3 | |
NM_001105078.3 | 3302 | Missense Mutation | ATG,CTG | M,L 1013 | NP_001098548.2 | |
NM_001163999.1 | 3302 | Missense Mutation | ATG,CTG | M,L 1005 | NP_001157471.1 | |
NM_001164000.1 | 3302 | Missense Mutation | ATG,CTG | M,L 1004 | NP_001157472.1 | |
NM_001205194.1 | 3302 | Missense Mutation | ATG,CTG | M,L 1013 | NP_001192123.1 | |
NM_004991.3 | 3302 | Missense Mutation | ATG,CTG | M,L 1201 | NP_004982.2 | |
NM_005241.3 | 3302 | Missense Mutation | ATG,CTG | M,L 1013 | NP_005232.2 | |
XM_005247213.3 | 3302 | Missense Mutation | ATG,CTG | M,L 1202 | XP_005247270.1 | |
XM_005247214.3 | 3302 | Missense Mutation | ATG,CTG | M,L 1193 | XP_005247271.1 | |
XM_005247215.3 | 3302 | Missense Mutation | ATG,CTG | M,L 1192 | XP_005247272.1 | |
XM_005247219.2 | 3302 | Missense Mutation | ATG,CTG | M,L 1014 | XP_005247276.1 | |
XM_005247220.2 | 3302 | Missense Mutation | ATG,CTG | M,L 1014 | XP_005247277.1 | |
XM_005247221.2 | 3302 | Missense Mutation | ATG,CTG | M,L 1014 | XP_005247278.1 | |
XM_005247223.2 | 3302 | Missense Mutation | ATG,CTG | M,L 1013 | XP_005247280.1 | |
XM_005247224.3 | 3302 | Missense Mutation | ATG,CTG | M,L 878 | XP_005247281.1 | |
XM_005247225.3 | 3302 | Missense Mutation | ATG,CTG | M,L 877 | XP_005247282.1 | |
XM_005247226.3 | 3302 | Missense Mutation | ATG,CTG | M,L 868 | XP_005247283.1 | |
XM_011512546.2 | 3302 | Missense Mutation | ATG,CTG | M,L 1086 | XP_011510848.1 | |
XM_017005874.1 | 3302 | Missense Mutation | ATG,CTG | M,L 1078 | XP_016861363.1 | |
XM_017005875.1 | 3302 | Missense Mutation | ATG,CTG | M,L 1004 | XP_016861364.1 | |
XM_017005876.1 | 3302 | Missense Mutation | ATG,CTG | M,L 1005 | XP_016861365.1 | |
XM_017005877.1 | 3302 | Missense Mutation | ATG,CTG | M,L 869 | XP_016861366.1 | |
XM_017005878.1 | 3302 | Missense Mutation | ATG,CTG | M,L 680 | XP_016861367.1 |