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AACCTTGAGACCCTGGCATACACTC[C/T]GGGGCGATTAGGCAGGGCACACTTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607247 MIM: 606635 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CHODL 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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CHODL - chondrolectin | ||||||
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There are no transcripts associated with this gene. |
TMPRSS15 - transmembrane protease, serine 15 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002772.2 | 3199 | Missense Mutation | NP_002763.2 | |||
XM_011529654.1 | 3199 | Nonsense Mutation | XP_011527956.1 | |||
XM_011529655.1 | 3199 | Nonsense Mutation | XP_011527957.1 | |||
XM_011529656.2 | 3199 | Nonsense Mutation | XP_011527958.1 | |||
XM_011529657.1 | 3199 | Nonsense Mutation | XP_011527959.1 | |||
XM_011529658.1 | 3199 | Nonsense Mutation | XP_011527960.1 | |||
XM_011529659.1 | 3199 | Nonsense Mutation | XP_011527961.1 |