Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600662 | |||||||||||||||||||||||||||||
Literature Links: |
MEF2C PubMed Links | |||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | JPT (Japanese)
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AFR - Not Available | Japanese - Not Available | CHB (Han Chinese)
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EUR - Not Available | |||||
AMR - Not Available |
MEF2C - myocyte enhancer factor 2C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001131005.2 | 1518 | Missense Mutation | TCT,TTT | S,F 458 | NP_001124477.1 | |
NM_001193347.1 | 1518 | Missense Mutation | TCT,TTT | S,F 478 | NP_001180276.1 | |
NM_001193348.1 | 1518 | Missense Mutation | TCT,TTT | S,F 412 | NP_001180277.1 | |
NM_001193349.1 | 1518 | Missense Mutation | TCT,TTT | S,F 388 | NP_001180278.1 | |
NM_001193350.1 | 1518 | Missense Mutation | TCT,TTT | S,F 468 | NP_001180279.1 | |
NM_001308002.1 | 1518 | Missense Mutation | TCT,TTT | S,F 460 | NP_001294931.1 | |
NM_002397.4 | 1518 | Missense Mutation | TCT,TTT | S,F 468 | NP_002388.2 | |
XM_005248511.2 | 1518 | Missense Mutation | TCT,TTT | S,F 468 | XP_005248568.1 | |
XM_006714619.2 | 1518 | Missense Mutation | TCT,TTT | S,F 468 | XP_006714682.1 | |
XM_006714625.3 | 1518 | Missense Mutation | TCT,TTT | S,F 478 | XP_006714688.1 | |
XM_011543396.2 | 1518 | Missense Mutation | TCT,TTT | S,F 468 | XP_011541698.1 | |
XM_011543397.2 | 1518 | Missense Mutation | TCT,TTT | S,F 466 | XP_011541699.1 | |
XM_011543400.1 | 1518 | Missense Mutation | TCT,TTT | S,F 436 | XP_011541702.1 | |
XM_011543401.1 | 1518 | Missense Mutation | TCT,TTT | S,F 428 | XP_011541703.1 | |
XM_017009475.1 | 1518 | Missense Mutation | TCT,TTT | S,F 466 | XP_016864964.1 | |
XM_017009476.1 | 1518 | Missense Mutation | TCT,TTT | S,F 460 | XP_016864965.1 | |
XM_017009477.1 | 1518 | Missense Mutation | TCT,TTT | S,F 460 | XP_016864966.1 | |
XM_017009478.1 | 1518 | Missense Mutation | TCT,TTT | S,F 458 | XP_016864967.1 | |
XM_017009479.1 | 1518 | Missense Mutation | TCT,TTT | S,F 436 | XP_016864968.1 | |
XM_017009480.1 | 1518 | Missense Mutation | TCT,TTT | S,F 436 | XP_016864969.1 | |
XM_017009481.1 | 1518 | Missense Mutation | TCT,TTT | S,F 436 | XP_016864970.1 | |
XM_017009482.1 | 1518 | Missense Mutation | TCT,TTT | S,F 428 | XP_016864971.1 | |
XM_017009483.1 | 1518 | Missense Mutation | TCT,TTT | S,F 426 | XP_016864972.1 |