Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCGTGGATGAGCAAAGGATGGAAG[A/G]AAACAGTGTCGCCCTTCTCCATCAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602026 | ||||||||||||||||||||
Literature Links: |
PHYH 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 |
PHYH - phytanoyl-CoA 2-hydroxylase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001037537.1 | 864 | Missense Mutation | TCC,TTC | S,F 157 | NP_001032626.1 | |
NM_001323080.1 | 864 | Missense Mutation | TCC,TTC | S,F 157 | NP_001310009.1 | |
NM_001323082.1 | 864 | Missense Mutation | TCC,TTC | S,F 259 | NP_001310011.1 | |
NM_001323083.1 | 864 | Missense Mutation | TCC,TTC | S,F 169 | NP_001310012.1 | |
NM_001323084.1 | 864 | Missense Mutation | TCC,TTC | S,F 159 | NP_001310013.1 | |
NM_006214.3 | 864 | Missense Mutation | TCC,TTC | S,F 257 | NP_006205.1 |