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CCTTGCATCATTCGGAACAACTTCA[C/T]TGGGCTCTTCTACAGAAAAAAATGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
HDX 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
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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HDX - highly divergent homeobox | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001177478.1 | 1770 | Missense Mutation | AAT,AGT | N,S 499 | NP_001170949.1 | |
NM_001177479.1 | 1770 | Missense Mutation | AAT,AGT | N,S 557 | NP_001170950.1 | |
NM_144657.4 | 1770 | Missense Mutation | AAT,AGT | N,S 557 | NP_653258.2 | |
XM_006724619.1 | 1770 | Missense Mutation | AAT,AGT | N,S 499 | XP_006724682.1 | |
XM_011530863.2 | 1770 | Missense Mutation | AAT,AGT | N,S 557 | XP_011529165.1 | |
XM_011530864.1 | 1770 | Missense Mutation | AAT,AGT | N,S 557 | XP_011529166.1 | |
XM_017029274.1 | 1770 | Missense Mutation | AAT,AGT | N,S 557 | XP_016884763.1 | |
XM_017029275.1 | 1770 | Missense Mutation | AAT,AGT | N,S 539 | XP_016884764.1 |