Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTCTGCTTTTACTATTTCAAACCAG[A/T]TGTTAAGCATGTTGAATTCAAATTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 613760 | ||||||||||||||||||||
Literature Links: |
SLC36A4 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
SLC36A4 - solute carrier family 36 member 4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286139.1 | 1644 | Missense Mutation | ACT,TCT | T,S 366 | NP_001273068.1 | |
NM_152313.3 | 1644 | Missense Mutation | ACT,TCT | T,S 501 | NP_689526.2 | |
XM_017017174.1 | 1644 | UTR 3 | XP_016872663.1 | |||
XM_017017175.1 | 1644 | Missense Mutation | ACT,TCT | T,S 395 | XP_016872664.1 | |
XM_017017176.1 | 1644 | Missense Mutation | ACT,TCT | T,S 366 | XP_016872665.1 | |
XM_017017177.1 | 1644 | UTR 3 | XP_016872666.1 |