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Search Thermo Fisher Scientific
CAGGACATGGGGTGGCTGGCCAGCC[C/G]TCTTCGCTACGACCCGCAGGTGTTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
4 submissions
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Phenotype: |
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Literature Links: |
MORN1 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 |
MORN1 - MORN repeat containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001301060.1 | 1321 | Intron | NP_001287989.1 | |||
NM_024848.2 | 1321 | Missense Mutation | ACG,AGG | T,R 465 | NP_079124.1 | |
XM_005244798.2 | 1321 | Missense Mutation | ACG,AGG | T,R 441 | XP_005244855.1 | |
XM_011542169.1 | 1321 | Missense Mutation | ACG,AGG | T,R 464 | XP_011540471.1 | |
XM_011542170.2 | 1321 | Intron | XP_011540472.1 | |||
XM_011542172.2 | 1321 | Intron | XP_011540474.1 | |||
XM_011542173.2 | 1321 | Intron | XP_011540475.1 | |||
XM_011542174.2 | 1321 | UTR 3 | XP_011540476.1 | |||
XM_011542176.1 | 1321 | Missense Mutation | ACG,AGG | T,R 368 | XP_011540478.1 | |
XM_011542177.1 | 1321 | Intron | XP_011540479.1 | |||
XM_017002365.1 | 1321 | Intron | XP_016857854.1 |