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CTGCAAAAGAGAGTTCACTCCTTCC[A/G]CTATTTTCATGTGAGTGTATCCAAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605719 MIM: 600404 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LAT2 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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LAT2 - linker for activation of T-cells family member 2 | ||||||
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There are no transcripts associated with this gene. |
RFC2 - replication factor C subunit 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278791.1 | 804 | Intron | NP_001265720.1 | |||
NM_001278792.1 | 804 | Intron | NP_001265721.1 | |||
NM_001278793.1 | 804 | Intron | NP_001265722.1 | |||
NM_002914.4 | 804 | Intron | NP_002905.2 | |||
NM_181471.2 | 804 | Intron | NP_852136.1 | |||
XM_006716080.2 | 804 | Missense Mutation | GCG,GTG | A,V 191 | XP_006716143.1 | |
XM_017012492.1 | 804 | Missense Mutation | GCG,GTG | A,V 227 | XP_016867981.1 | |
XM_017012493.1 | 804 | Missense Mutation | GCG,GTG | A,V 191 | XP_016867982.1 |