Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCATTCAGTCTCACACCACTGTTCA[C/T]AAGATTAGCAGCCAACTGCCAATTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601688 | ||||||||||||||||||||
Literature Links: |
HPGD 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 |
HPGD - hydroxyprostaglandin dehydrogenase 15-(NAD) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000860.5 | 691 | Missense Mutation | ATG,GTG | M,V 172 | NP_000851.2 | |
NM_001145816.2 | 691 | Intron | NP_001139288.1 | |||
NM_001256301.1 | 691 | Missense Mutation | ATG,GTG | M,V 51 | NP_001243230.1 | |
NM_001256305.1 | 691 | Intron | NP_001243234.1 | |||
NM_001256306.1 | 691 | Missense Mutation | ATG,GTG | M,V 104 | NP_001243235.1 | |
NM_001256307.1 | 691 | Missense Mutation | ATG,GTG | M,V 51 | NP_001243236.1 | |
XM_011531907.1 | 691 | Intron | XP_011530209.1 |