Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGTTGGTCTTTCAGCTGTGGTCGCC[A/G]GGACCCCCCCAGAGCCAAGACCTTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 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 |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
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 | 326 | Missense Mutation | AGG,GGG | R,G 20 | NP_001273294.1 | |
NM_001286366.1 | 326 | Missense Mutation | AGG,GGG | R,G 20 | NP_001273295.1 | |
NM_018067.4 | 326 | Missense Mutation | AGG,GGG | R,G 20 | NP_060537.3 | |
XM_005271027.1 | 326 | Missense Mutation | AGG,GGG | R,G 20 | XP_005271084.1 | |
XM_006710759.1 | 326 | Missense Mutation | AGG,GGG | R,G 20 | XP_006710822.1 | |
XM_006710761.1 | 326 | Missense Mutation | AGG,GGG | R,G 20 | XP_006710824.1 |