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CATTGGTGTGGAAGGCCTGGAAGTC[G/T]ATCTGCTGGTTGAGGGGGCAGCCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607362 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RGMA 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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RGMA - repulsive guidance molecule family member a | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001166283.1 | 1230 | Silent Mutation | NP_001159755.1 | |||
NM_001166286.1 | 1230 | Silent Mutation | NP_001159758.1 | |||
NM_001166287.1 | 1230 | Silent Mutation | NP_001159759.1 | |||
NM_001166288.1 | 1230 | Silent Mutation | NP_001159760.1 | |||
NM_001166289.1 | 1230 | Silent Mutation | NP_001159761.1 | |||
NM_020211.2 | 1230 | Silent Mutation | NP_064596.2 |