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TGATGCTCACCTTCCTCTACCTCTT[C/T]GTCTGCTCCCTGGACATGCTCAGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 182309 | ||||||||||||||||||||
Literature Links: |
SLC34A1 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 |
SLC34A1 - solute carrier family 34 member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001167579.1 | 389 | Silent Mutation | TTC,TTT | F,F 114 | NP_001161051.1 | |
NM_003052.4 | 389 | Silent Mutation | TTC,TTT | F,F 114 | NP_003043.3 | |
XM_005265975.1 | 389 | Silent Mutation | TTC,TTT | F,F 114 | XP_005266032.1 | |
XM_017009773.1 | 389 | Silent Mutation | TTC,TTT | F,F 114 | XP_016865262.1 | |
XM_017009774.1 | 389 | Intron | XP_016865263.1 | |||
XM_017009775.1 | 389 | Silent Mutation | TTC,TTT | F,F 114 | XP_016865264.1 |