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AGGAGAGAGTGTGCTTATTGCCTAA[A/C]CATCAACACCACCATCTGTGCTGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
4 submissions
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Phenotype: |
MIM: 188540 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TSHB 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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TSHB - thyroid stimulating hormone beta | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000549.4 | 160 | Missense Mutation | AAC,ACC | N,T 41 | NP_000540.2 | |
NM_001277991.1 | 160 | Intron | NP_001264920.1 | |||
XM_011542065.2 | 160 | Missense Mutation | AAC,ACC | N,T 41 | XP_011540367.1 |