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GGTTGAACGCTGCTGGTTACGCGGA[C/T]GGGCAGGCGCAGCCGCAGCAGCCGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604434 MIM: 605539 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KLK11 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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KLK11 - kallikrein related peptidase 11 | ||||||
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There are no transcripts associated with this gene. |
KLK12 - kallikrein related peptidase 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_019598.2 | 469 | Missense Mutation | NP_062544.1 | |||
NM_145894.1 | 469 | Missense Mutation | NP_665901.1 | |||
NM_145895.1 | 469 | Intron | NP_665902.1 | |||
XM_005258950.3 | 469 | Intron | XP_005259007.1 | |||
XM_005258951.3 | 469 | Intron | XP_005259008.1 |