Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCTGCCTCCACCCCACAAGCTGCGG[C/T]GGCTGCCCCCCACCTCTGCCCGGCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 106195 | ||||||||||||||||||||
Literature Links: |
SLC4A3 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 |
SLC4A3 - solute carrier family 4 member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001326559.1 | 689 | Missense Mutation | CGG,TGG | R,W 97 | NP_001313488.1 | |
NM_005070.3 | 689 | Missense Mutation | CGG,TGG | R,W 97 | NP_005061.2 | |
NM_201574.2 | 689 | Missense Mutation | CGG,TGG | R,W 97 | NP_963868.2 | |
XM_005246789.4 | 689 | Missense Mutation | CGG,TGG | R,W 97 | XP_005246846.1 | |
XM_005246790.4 | 689 | Intron | XP_005246847.1 | |||
XM_011511665.2 | 689 | Missense Mutation | CGG,TGG | R,W 44 | XP_011509967.1 | |
XM_011511667.2 | 689 | Intron | XP_011509969.1 |