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CTCGGGCTGTCCTCCGCATACCTCC[C/T]TCACGTTGGCAACCTGTGCCTGGTG
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
HSPC102 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)
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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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HSPC102 - uncharacterized HSPC102 | ||||||
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There are no transcripts associated with this gene. |
TSPAN16 - tetraspanin 16 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282509.1 | 254 | Missense Mutation | CCT,CTT | P,L 55 | NP_001269438.1 | |
NM_001282510.1 | 254 | Missense Mutation | CCT,CTT | P,L 55 | NP_001269439.1 | |
NM_012466.3 | 254 | Missense Mutation | CCT,CTT | P,L 55 | NP_036598.1 | |
XM_011527901.1 | 254 | Missense Mutation | CCT,CTT | P,L 55 | XP_011526203.1 | |
XM_011527902.1 | 254 | Missense Mutation | CCT,CTT | P,L 55 | XP_011526204.1 | |
XM_011527903.2 | 254 | UTR 5 | XP_011526205.1 |