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Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601802 | |||||||||||||||||||||||
Literature Links: |
HESX1 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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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 |
HESX1 - HESX homeobox 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003865.2 | 602 | Missense Mutation | AAT,AGT | N,S 125 | NP_003856.1 | |
XM_005265526.4 | 602 | Missense Mutation | AAT,AGT | N,S 125 | XP_005265583.1 | |
XM_006713379.3 | 602 | Missense Mutation | AAT,AGT | N,S 125 | XP_006713442.1 | |
XM_011534204.2 | 602 | Missense Mutation | AAT,AGT | N,S 125 | XP_011532506.1 | |
XM_011534205.2 | 602 | Missense Mutation | AAT,AGT | N,S 125 | XP_011532507.1 | |
XM_017007421.1 | 602 | Missense Mutation | AAT,AGT | N,S 125 | XP_016862910.1 |