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TCCCAACCAAAACCAGAAGCAGGGC[A/C]GCTTCCGCAGCCTGGAGGAAGCACT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605788 MIM: 615301 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MAPRE3 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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MAPRE3 - microtubule associated protein RP/EB family member 3 | ||||||
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There are no transcripts associated with this gene. |
TMEM214 - transmembrane protein 214 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001083590.1 | 402 | Missense Mutation | AGC,CGC | S,R 107 | NP_001077059.1 | |
NM_017727.4 | 402 | Missense Mutation | AGC,CGC | S,R 107 | NP_060197.4 | |
XM_005264381.3 | 402 | Missense Mutation | AGC,CGC | S,R 107 | XP_005264438.1 | |
XM_005264382.3 | 402 | Missense Mutation | AGC,CGC | S,R 107 | XP_005264439.1 | |
XM_005264383.3 | 402 | Intron | XP_005264440.1 |