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TGCTGTTTGCAATGACCTCCGCTGG[A/G]ACATGTGAGTCCTGTAGGGTCGATT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606765 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TPO 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
|
TPO - thyroid peroxidase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000547.5 | Intron | NP_000538.3 | ||||
NM_001206744.1 | Intron | NP_001193673.1 | ||||
NM_001206745.1 | Intron | NP_001193674.1 | ||||
NM_175719.3 | Intron | NP_783650.1 | ||||
NM_175721.3 | Intron | NP_783652.1 | ||||
NM_175722.3 | Intron | NP_783653.1 | ||||
XM_011510379.2 | Intron | XP_011508681.1 | ||||
XM_011510380.2 | Intron | XP_011508682.1 | ||||
XM_011510381.2 | Intron | XP_011508683.1 |