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CGTCACAGAAGAAAAAGAAAAAGTC[C/G]AGCCCACAGTCTACTGATACAGCTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604702 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HMGXB4 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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HMGXB4 - HMG-box containing 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001003681.2 | 477 | Silent Mutation | TCC,TCG | S,S 101 | NP_001003681.1 | |
XM_006724100.3 | 477 | Silent Mutation | TCC,TCG | S,S 144 | XP_006724163.1 | |
XM_006724101.3 | 477 | Silent Mutation | TCC,TCG | S,S 144 | XP_006724164.1 | |
XM_006724102.1 | 477 | UTR 5 | XP_006724165.1 |