Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCTGTCGATTGTTCTTTCTGTTCAG[A/G]TTCTGTTGGGAGTTTGGGGGAGCAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601746 | ||||||||||||||||||||
Literature Links: |
HYOU1 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 |
HYOU1 - hypoxia up-regulated 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001130991.2 | 3039 | Missense Mutation | CCT,TCT | P,S 981 | NP_001124463.1 | |
NM_006389.4 | 3039 | Missense Mutation | CCT,TCT | P,S 981 | NP_006380.1 | |
XM_005271392.3 | 3039 | Missense Mutation | CCT,TCT | P,S 982 | XP_005271449.1 | |
XM_005271393.3 | 3039 | Missense Mutation | CCT,TCT | P,S 982 | XP_005271450.1 | |
XM_005271394.3 | 3039 | Missense Mutation | CCT,TCT | P,S 982 | XP_005271451.1 | |
XM_017017095.1 | 3039 | Missense Mutation | CCT,TCT | P,S 982 | XP_016872584.1 | |
XM_017017096.1 | 3039 | Missense Mutation | CCT,TCT | P,S 981 | XP_016872585.1 | |
XM_017017097.1 | 3039 | Missense Mutation | CCT,TCT | P,S 981 | XP_016872586.1 |