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TAACTCAGTGTGGCGTTAGCGATGC[C/T]TTTTCATGGTGTCATTTATCCACTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602652 MIM: 604438 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KLK6 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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KLK6 - kallikrein related peptidase 6 | ||||||
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There are no transcripts associated with this gene. |
KLK7 - kallikrein related peptidase 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001207053.1 | 1024 | Missense Mutation | AAG,AGG | K,R 179 | NP_001193982.1 | |
NM_001243126.1 | 1024 | Missense Mutation | AAG,AGG | K,R 244 | NP_001230055.1 | |
NM_005046.3 | 1024 | Missense Mutation | AAG,AGG | K,R 251 | NP_005037.1 | |
NM_139277.2 | 1024 | Missense Mutation | AAG,AGG | K,R 251 | NP_644806.1 |