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TGGTACATTTCTGCCGTCAGGGGCC[A/G]GAAGGACTGGGCCCGGTTGTCCAGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603314 | ||||||||||||||||||||
Literature Links: |
SLC27A5 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 |
SLC27A5 - solute carrier family 27 member 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321196.1 | 2127 | Missense Mutation | CGG,TGG | R,W 589 | NP_001308125.1 | |
NM_012254.2 | 2127 | Missense Mutation | CGG,TGG | R,W 673 | NP_036386.1 | |
XM_011526364.1 | 2127 | UTR 3 | XP_011524666.1 | |||
XM_017026214.1 | 2127 | Intron | XP_016881703.1 |
ZNF446 - zinc finger protein 446 | ||||||
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There are no transcripts associated with this gene. |