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AGGATGCATCCCAACCTTACCAAGG[C/G]CTTCGGCATGATTGGCCCCAAGGAC
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 |
---|---|---|
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 |
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 | 1015 | Missense Mutation | GCC,GGC | A,G 266 | NP_001077059.1 | |
NM_017727.4 | 1015 | Missense Mutation | GCC,GGC | A,G 311 | NP_060197.4 | |
XM_005264381.3 | 1015 | Missense Mutation | GCC,GGC | A,G 311 | XP_005264438.1 | |
XM_005264382.3 | 1015 | Missense Mutation | GCC,GGC | A,G 311 | XP_005264439.1 | |
XM_005264383.3 | 1015 | Intron | XP_005264440.1 |