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GCTGCTCACAGTCACCGCTGTCATT[C/G]TGGGTGAGTCATTTGATTAAAAACA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600111 | ||||||||||||||||||||
Literature Links: |
SLC1A3 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 |
SLC1A3 - solute carrier family 1 member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001166695.2 | 403 | Missense Mutation | CTG,GTG | L,V 60 | NP_001160167.1 | |
NM_001166696.2 | 403 | Missense Mutation | CTG,GTG | L,V 60 | NP_001160168.1 | |
NM_001289939.1 | 403 | Missense Mutation | CTG,GTG | L,V 60 | NP_001276868.1 | |
NM_001289940.1 | 403 | Missense Mutation | CTG,GTG | L,V 60 | NP_001276869.1 | |
NM_004172.4 | 403 | Missense Mutation | CTG,GTG | L,V 60 | NP_004163.3 | |
XM_005248342.2 | 403 | Missense Mutation | CTG,GTG | L,V 60 | XP_005248399.1 | |
XM_011514084.2 | 403 | UTR 5 | XP_011512386.1 |