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TCACTCAGGGCTCGGCACTCCACAG[A/C]GTTCTGGATGGTTTCCAGGGCCCGA
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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
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 | 386 | Missense Mutation | CGC,CTC | R,L 78 | NP_001074466.1 | |
NM_001270440.1 | 386 | Missense Mutation | CGC,CTC | R,L 110 | NP_001257369.1 | |
NM_001270441.1 | 386 | Missense Mutation | CGC,CTC | R,L 88 | NP_001257370.1 | |
NM_001270442.1 | 386 | Missense Mutation | CGC,CTC | R,L 84 | NP_001257371.1 | |
NM_001270443.1 | 386 | Missense Mutation | CGC,CTC | R,L 78 | NP_001257372.1 | |
NM_001270444.1 | 386 | Missense Mutation | CGC,CTC | R,L 78 | NP_001257373.1 | |
NM_001270445.1 | 386 | Missense Mutation | CGC,CTC | R,L 72 | NP_001257374.1 | |
NM_031429.2 | 386 | Missense Mutation | CGC,CTC | R,L 110 | NP_113617.1 | |
XM_005260089.1 | 386 | Missense Mutation | CGC,CTC | R,L 135 | XP_005260146.1 | |
XM_005260090.3 | 386 | Missense Mutation | CGC,CTC | R,L 113 | XP_005260147.1 | |
XM_011528343.1 | 386 | Missense Mutation | CGC,CTC | R,L 130 | XP_011526645.1 | |
XM_011528344.2 | 386 | Missense Mutation | CGC,CTC | R,L 113 | XP_011526646.1 | |
XM_011528345.1 | 386 | Missense Mutation | CGC,CTC | R,L 103 | XP_011526647.1 | |
XM_017027343.1 | 386 | Missense Mutation | CGC,CTC | R,L 120 | XP_016882832.1 | |
XM_017027344.1 | 386 | Missense Mutation | CGC,CTC | R,L 104 | XP_016882833.1 |