Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTCTGAGCGCCGCCACTTTGCCAGG[C/T]GCTGCTTAAACCATTTCTGGAAGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 607275 | ||||||||||||||||||||
Literature Links: |
HOPX PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
HOPX - HOP homeobox | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145459.1 | 628 | Missense Mutation | NP_001138931.1 | |||
NM_001145460.1 | 628 | UTR 3 | NP_001138932.1 | |||
NM_032495.5 | 628 | Missense Mutation | NP_115884.4 | |||
NM_139211.4 | 628 | Missense Mutation | NP_631957.1 | |||
NM_139212.3 | 628 | Missense Mutation | NP_631958.1 | |||
XM_006714052.2 | 628 | Intron | XP_006714115.1 | |||
XM_017008728.1 | 628 | Missense Mutation | XP_016864217.1 | |||
XM_017008729.1 | 628 | Missense Mutation | XP_016864218.1 | |||
XM_017008730.1 | 628 | Missense Mutation | XP_016864219.1 | |||
XM_017008731.1 | 628 | Missense Mutation | XP_016864220.1 | |||
XM_017008732.1 | 628 | Missense Mutation | XP_016864221.1 | |||
XM_017008733.1 | 628 | Missense Mutation | XP_016864222.1 | |||
XM_017008734.1 | 628 | Missense Mutation | XP_016864223.1 |