Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603947 | ||||||||||||||||||||
Literature Links: |
EML3 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 |
EML3 - echinoderm microtubule associated protein like 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001300793.1 | 3362 | Missense Mutation | ACT,CCT | T,P 858 | NP_001287722.1 | |
NM_001300794.1 | 3362 | Missense Mutation | ACT,CCT | T,P 857 | NP_001287723.1 | |
NM_153265.2 | 3362 | Silent Mutation | TCA,TCC | S,S 893 | NP_694997.2 | |
XM_005273878.3 | 3362 | Silent Mutation | TCA,TCC | S,S 894 | XP_005273935.1 | |
XM_006718489.3 | 3362 | Missense Mutation | ACT,CCT | T,P 908 | XP_006718552.1 | |
XM_006718490.3 | 3362 | Silent Mutation | TCA,TCC | S,S 944 | XP_006718553.1 | |
XM_006718491.3 | 3362 | Silent Mutation | TCA,TCC | S,S 943 | XP_006718554.1 | |
XM_011544896.2 | 3362 | Missense Mutation | ACT,CCT | T,P 907 | XP_011543198.1 | |
XM_011544897.2 | 3362 | Missense Mutation | ACT,CCT | T,P 856 | XP_011543199.1 | |
XM_017017480.1 | 3362 | Missense Mutation | ACT,CCT | T,P 741 | XP_016872969.1 | |
XM_017017481.1 | 3362 | Missense Mutation | ACT,CCT | T,P 741 | XP_016872970.1 | |
XM_017017482.1 | 3362 | Silent Mutation | TCA,TCC | S,S 777 | XP_016872971.1 | |
XM_017017483.1 | 3362 | Missense Mutation | ACT,CCT | T,P 640 | XP_016872972.1 |
MTA2 - metastasis associated 1 family member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004739.3 | 3362 | Intron | NP_004730.2 | |||
XM_017018561.1 | 3362 | Intron | XP_016874050.1 |