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GGCCTTCTGGCACACCTCATCCGGG[A/G]AGATGTTGATGTTCACGCATTGCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606135 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KLK14 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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KLK14 - kallikrein related peptidase 14 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001311182.1 | 741 | Missense Mutation | TCC,TTC | S,F 186 | NP_001298111.1 | |
NM_022046.5 | 741 | Missense Mutation | TCC,TTC | S,F 186 | NP_071329.2 | |
XM_017026820.1 | 741 | UTR 3 | XP_016882309.1 |