Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612256 MIM: 609553 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
MAST1 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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MAST1 - microtubule associated serine/threonine kinase 1 | ||||||
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There are no transcripts associated with this gene. |
RTBDN - retbindin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080997.2 | 746 | Missense Mutation | GCC,GGC | A,G 198 | NP_001074466.1 | |
NM_001270440.1 | 746 | UTR 3 | NP_001257369.1 | |||
NM_001270441.1 | 746 | Missense Mutation | GCC,GGC | A,G 208 | NP_001257370.1 | |
NM_001270442.1 | 746 | Missense Mutation | GCC,GGC | A,G 204 | NP_001257371.1 | |
NM_001270443.1 | 746 | Missense Mutation | GCC,GGC | A,G 198 | NP_001257372.1 | |
NM_001270444.1 | 746 | Missense Mutation | GCC,GGC | A,G 198 | NP_001257373.1 | |
NM_001270445.1 | 746 | Missense Mutation | GCC,GGC | A,G 192 | NP_001257374.1 | |
NM_031429.2 | 746 | Missense Mutation | GCC,GGC | A,G 230 | NP_113617.1 | |
XM_005260089.1 | 746 | Missense Mutation | GCC,GGC | A,G 255 | XP_005260146.1 | |
XM_005260090.3 | 746 | Missense Mutation | GCC,GGC | A,G 233 | XP_005260147.1 | |
XM_011528343.1 | 746 | Missense Mutation | GCC,GGC | A,G 250 | XP_011526645.1 | |
XM_011528344.2 | 746 | Missense Mutation | GCC,GGC | A,G 233 | XP_011526646.1 | |
XM_011528345.1 | 746 | Missense Mutation | GCC,GGC | A,G 223 | XP_011526647.1 | |
XM_017027343.1 | 746 | Missense Mutation | GCC,GGC | A,G 240 | XP_016882832.1 | |
XM_017027344.1 | 746 | Missense Mutation | GCC,GGC | A,G 224 | XP_016882833.1 |