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GGTCTTTCAGCTGTGGTCGCCAGGA[C/T]CCCCCCAGAGCCAAGACCTTCTCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
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Literature Links: |
MAP7D1 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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MAP7D1 - MAP7 domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286365.1 | 330 | Missense Mutation | ACC,ATC | T,I 21 | NP_001273294.1 | |
NM_001286366.1 | 330 | Missense Mutation | ACC,ATC | T,I 21 | NP_001273295.1 | |
NM_018067.4 | 330 | Missense Mutation | ACC,ATC | T,I 21 | NP_060537.3 | |
XM_005271027.1 | 330 | Missense Mutation | ACC,ATC | T,I 21 | XP_005271084.1 | |
XM_006710759.1 | 330 | Missense Mutation | ACC,ATC | T,I 21 | XP_006710822.1 | |
XM_006710761.1 | 330 | Missense Mutation | ACC,ATC | T,I 21 | XP_006710824.1 |