Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602673 MIM: 604434 MIM: 605539 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
KLK10 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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KLK10 - kallikrein related peptidase 10 | ||||||
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There are no transcripts associated with this gene. |
KLK11 - kallikrein related peptidase 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136032.2 | 529 | Missense Mutation | CGC,TGC | R,C 134 | NP_001129504.1 | |
NM_001167605.1 | 529 | Missense Mutation | CGC,TGC | R,C 159 | NP_001161077.1 | |
NM_006853.2 | 529 | Missense Mutation | CGC,TGC | R,C 134 | NP_006844.1 | |
NM_144947.1 | 529 | Missense Mutation | CGC,TGC | R,C 166 | NP_659196.1 | |
XM_005258439.3 | 529 | Intron | XP_005258496.1 | |||
XM_011526369.1 | 529 | Missense Mutation | CGC,TGC | R,C 191 | XP_011524671.1 | |
XM_011526370.2 | 529 | Missense Mutation | CGC,TGC | R,C 159 | XP_011524672.1 | |
XM_011526371.2 | 529 | Missense Mutation | CGC,TGC | R,C 159 | XP_011524673.1 | |
XM_011526372.2 | 529 | Missense Mutation | CGC,TGC | R,C 159 | XP_011524674.1 | |
XM_011526373.1 | 529 | Missense Mutation | CGC,TGC | R,C 159 | XP_011524675.1 |
KLK12 - kallikrein related peptidase 12 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |