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CGAACACAGCACTGATGAGGGACTG[C/T]AGGCCTGTCAGCGTCCCAAAGTGGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610462 MIM: 603733 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RTN4RL2 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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RTN4RL2 - reticulon 4 receptor-like 2 | ||||||
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There are no transcripts associated with this gene. |
SLC43A1 - solute carrier family 43 member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001198810.1 | 1541 | Silent Mutation | CTA,CTG | L,L 482 | NP_001185739.1 | |
NM_003627.5 | 1541 | Silent Mutation | CTA,CTG | L,L 482 | NP_003618.1 | |
XM_005274358.4 | 1541 | Silent Mutation | CTA,CTG | L,L 498 | XP_005274415.1 | |
XM_011545320.2 | 1541 | Silent Mutation | CTA,CTG | L,L 467 | XP_011543622.1 | |
XM_011545321.2 | 1541 | Silent Mutation | CTA,CTG | L,L 226 | XP_011543623.1 | |
XM_011545322.1 | 1541 | Silent Mutation | CTA,CTG | L,L 226 | XP_011543624.1 | |
XM_017018451.1 | 1541 | Silent Mutation | CTA,CTG | L,L 482 | XP_016873940.1 | |
XM_017018452.1 | 1541 | Silent Mutation | CTA,CTG | L,L 451 | XP_016873941.1 | |
XM_017018453.1 | 1541 | Silent Mutation | CTA,CTG | L,L 226 | XP_016873942.1 |