Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGGCGCGCTGCTGGCCTGGTGCCGC[C/T]GCCAGTGCGAGGGCTACCGCGGCGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
MICALL1 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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MICALL1 - MICAL like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_033386.3 | 128 | Missense Mutation | CGC,TGC | R,C 14 | NP_203744.1 | |
XM_005261791.3 | 128 | Missense Mutation | CGC,TGC | R,C 14 | XP_005261848.1 | |
XM_005261792.3 | 128 | Missense Mutation | CGC,TGC | R,C 14 | XP_005261849.1 | |
XM_011530471.2 | 128 | Missense Mutation | CGC,TGC | R,C 14 | XP_011528773.1 | |
XM_011530472.2 | 128 | Missense Mutation | CGC,TGC | R,C 14 | XP_011528774.1 | |
XM_011530473.2 | 128 | Missense Mutation | CGC,TGC | R,C 14 | XP_011528775.1 | |
XM_011530474.2 | 128 | Intron | XP_011528776.1 | |||
XM_011530475.2 | 128 | UTR 5 | XP_011528777.1 | |||
XM_011530476.2 | 128 | Missense Mutation | CGC,TGC | R,C 14 | XP_011528778.1 | |
XM_017029026.1 | 128 | UTR 5 | XP_016884515.1 |