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CCCTACCTCAATGCTGACCGTCCGC[C/T]GCTGGGCCACTGGCAGCTTCAGACA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300060 MIM: 312090 MIM: 312070 | ||||||||||||||||||||
Literature Links: |
LAGE3 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 |
LAGE3 - L antigen family member 3 | ||||||
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There are no transcripts associated with this gene. |
SLC10A3 - solute carrier family 10 member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142391.2 | 1623 | Missense Mutation | CAG,CGG | Q,R 385 | NP_001135863.1 | |
NM_001142392.2 | 1623 | Missense Mutation | CAG,CGG | Q,R 414 | NP_001135864.1 | |
NM_019848.4 | 1623 | Missense Mutation | CAG,CGG | Q,R 414 | NP_062822.1 | |
XM_005277913.4 | 1623 | Missense Mutation | CAG,CGG | Q,R 469 | XP_005277970.1 | |
XM_006724847.3 | 1623 | Missense Mutation | CAG,CGG | Q,R 507 | XP_006724910.1 | |
XM_006724848.3 | 1623 | Missense Mutation | CAG,CGG | Q,R 478 | XP_006724911.1 | |
XM_011531200.2 | 1623 | Missense Mutation | CAG,CGG | Q,R 469 | XP_011529502.2 | |
XM_011531201.2 | 1623 | Missense Mutation | CAG,CGG | Q,R 414 | XP_011529503.1 |
UBL4A - ubiquitin like 4A | ||||||
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There are no transcripts associated with this gene. |