Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGTTGGTGATGGACAAGAGAGCCT[C/T]AGGAATGAATGACTCATTGGAGTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616714 | ||||||||||||||||||||
Literature Links: |
HBP1 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 |
HBP1 - HMG-box transcription factor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001244262.1 | 263 | Missense Mutation | TCA,TTA | S,L 36 | NP_001231191.1 | |
NM_012257.3 | 263 | Missense Mutation | TCA,TTA | S,L 26 | NP_036389.2 | |
XM_005250266.2 | 263 | Missense Mutation | TCA,TTA | S,L 26 | XP_005250323.1 | |
XM_005250267.2 | 263 | Missense Mutation | TCA,TTA | S,L 26 | XP_005250324.1 | |
XM_017011967.1 | 263 | Missense Mutation | TCA,TTA | S,L 26 | XP_016867456.1 |