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TTGGCACAATGCAACGTATCTGGGA[A/G]ACTCACTGGGGAAGACAGTGGACTT
Species: |
Human | ||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 147910 MIM: 610601 | ||||||||||||||||||||||||||
Literature Links: |
KLK1 PubMed Links | ||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | JPT (Japanese)
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AFR - Not Available | Japanese - Not Available | CHB (Han Chinese)
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EUR - Not Available | |||||
AMR - Not Available |
KLK1 - kallikrein 1 | ||||||
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There are no transcripts associated with this gene. |
KLK15 - kallikrein related peptidase 15 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001277081.1 | 1315 | Missense Mutation | CTC,TTC | L,F 162 | NP_001264010.1 | |
NM_001277082.1 | 1315 | Intron | NP_001264011.1 | |||
NM_017509.3 | 1315 | Missense Mutation | CTC,TTC | L,F 163 | NP_059979.2 | |
XM_006723265.3 | 1315 | Missense Mutation | CTC,TTC | L,F 163 | XP_006723328.1 | |
XM_011527085.2 | 1315 | Missense Mutation | CTC,TTC | L,F 162 | XP_011525387.1 | |
XM_011527087.2 | 1315 | Intron | XP_011525389.1 | |||
XM_011527088.2 | 1315 | Intron | XP_011525390.1 | |||
XM_011527089.2 | 1315 | Intron | XP_011525391.1 | |||
XM_017026943.1 | 1315 | UTR 3 | XP_016882432.1 |
LOC105372441 - uncharacterized LOC105372441 | ||||||
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There are no transcripts associated with this gene. |
MGC45922 - uncharacterized LOC284365 | ||||||
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There are no transcripts associated with this gene. |
Set Membership: |
HapMap |