Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCAAACACGGAGGCACGTAGGAGTC[C/T]GGGGCCATGTGGTCGGTTTCTTTAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
MICALL2 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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MICALL2 - MICAL like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_182924.3 | 3074 | UTR 3 | NP_891554.1 | |||
XM_011515520.2 | 3074 | Missense Mutation | CAG,CGG | Q,R 982 | XP_011513822.1 | |
XM_011515522.2 | 3074 | Missense Mutation | CAG,CGG | Q,R 968 | XP_011513824.1 | |
XM_011515523.2 | 3074 | Missense Mutation | CAG,CGG | Q,R 899 | XP_011513825.1 | |
XM_011515524.2 | 3074 | Missense Mutation | CAG,CGG | Q,R 411 | XP_011513826.1 | |
XM_017012619.1 | 3074 | Intron | XP_016868108.1 |