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Search Thermo Fisher Scientific
AGAACCAGGCGGGCGTCGTGGGAGC[A/G]CGTGACAATGACTTCATTGAGCTTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606967 MIM: 176847 MIM: 604119 | ||||||||||||||||||||
Literature Links: |
LCAT PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
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 | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
LCAT - lecithin-cholesterol acyltransferase | ||||||
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There are no transcripts associated with this gene. |
PSMB10 - proteasome subunit beta 10 | ||||||
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There are no transcripts associated with this gene. |
SLC12A4 - solute carrier family 12 member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145961.1 | 3114 | Missense Mutation | CGC,TGC | R,C 1026 | NP_001139433.1 | |
NM_001145962.1 | 3114 | Missense Mutation | CGC,TGC | R,C 1034 | NP_001139434.1 | |
NM_001145963.1 | 3114 | Missense Mutation | CGC,TGC | R,C 1026 | NP_001139435.1 | |
NM_001145964.1 | 3114 | Missense Mutation | CGC,TGC | R,C 1001 | NP_001139436.1 | |
NM_005072.4 | 3114 | Missense Mutation | CGC,TGC | R,C 1032 | NP_005063.1 |