Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGTCTCTACAAAAATCTCATTGTG[A/G]CTTCGAGGGCTTGTCTGTGGCAGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603159 MIM: 607959 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LRP3 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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LRP3 - LDL receptor related protein 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002333.3 | 1346 | Intron | NP_002324.2 | |||
XM_005258945.1 | 1346 | Intron | XP_005259002.1 |
SLC7A10 - solute carrier family 7 member 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_019849.2 | 1346 | Missense Mutation | CCA,TCA | P,S 522 | NP_062823.1 | |
XM_006723284.2 | 1346 | Missense Mutation | CCA,TCA | P,S 443 | XP_006723347.1 | |
XM_011527119.1 | 1346 | Missense Mutation | CCA,TCA | P,S 659 | XP_011525421.1 | |
XM_011527120.1 | 1346 | Missense Mutation | CCA,TCA | P,S 632 | XP_011525422.1 |