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CCCCCACAGGCCAGCGGAGCCTGCA[C/T]CACCGTGGAGACAACCTGGAGACCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607573 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MAP1S 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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MAP1S - microtubule associated protein 1S | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308363.1 | 629 | Silent Mutation | CAC,CAT | H,H 53 | NP_001295292.1 | |
NM_018174.5 | 629 | Silent Mutation | CAC,CAT | H,H 79 | NP_060644.4 | |
XM_017026930.1 | 629 | Silent Mutation | CAC,CAT | H,H 79 | XP_016882419.1 | |
XM_017026931.1 | 629 | Silent Mutation | CAC,CAT | H,H 53 | XP_016882420.1 |