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AATGTGCTGCTGCTCACAGCTCCAA[C/T]GAAGGAAATCACAATGTCTAAACGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613760 | ||||||||||||||||||||
Literature Links: |
SLC36A4 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 |
SLC36A4 - solute carrier family 36 member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286139.1 | 1398 | Missense Mutation | ATT,GTT | I,V 284 | NP_001273068.1 | |
NM_152313.3 | 1398 | Missense Mutation | ATT,GTT | I,V 419 | NP_689526.2 | |
XM_017017174.1 | 1398 | UTR 3 | XP_016872663.1 | |||
XM_017017175.1 | 1398 | Missense Mutation | ATT,GTT | I,V 313 | XP_016872664.1 | |
XM_017017176.1 | 1398 | Missense Mutation | ATT,GTT | I,V 284 | XP_016872665.1 | |
XM_017017177.1 | 1398 | UTR 3 | XP_016872666.1 |