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CGCTGAGAGGGAGATGTGTTGGGTG[C/T]GGGGCCTGGGCCGCCGCTCTCGCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
LACE1 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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LACE1 - lactation elevated 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001323005.1 | 167 | Silent Mutation | TGC,TGT | C,C 26 | NP_001309934.1 | |
NM_145315.4 | 167 | Silent Mutation | TGC,TGT | C,C 26 | NP_660358.2 | |
XM_005266885.3 | 167 | Intron | XP_005266942.1 | |||
XM_011535657.2 | 167 | Missense Mutation | TGC,TGT | C,C 26 | XP_011533959.1 | |
XM_011535659.2 | 167 | Missense Mutation | TGC,TGT | C,C 26 | XP_011533961.1 | |
XM_011535660.2 | 167 | Missense Mutation | TGC,TGT | C,C 26 | XP_011533962.1 | |
XM_011535661.2 | 167 | Missense Mutation | TGC,TGT | C,C 26 | XP_011533963.1 | |
XM_017010647.1 | 167 | Intron | XP_016866136.1 | |||
XM_017010648.1 | 167 | Intron | XP_016866137.1 | |||
XM_017010649.1 | 167 | UTR 5 | XP_016866138.1 |