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CGGCCTGGGGGCTGTCCAGCACGTC[A/G]ATGGCCAGCGTGTACGGGTCGAACT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 176730 MIM: 191290 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
INS 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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INS - insulin | ||||||
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There are no transcripts associated with this gene. |
INS-IGF2 - INS-IGF2 readthrough | ||||||
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There are no transcripts associated with this gene. |
MIR4686 - microRNA 4686 | ||||||
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There are no transcripts associated with this gene. |
TH - tyrosine hydroxylase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000360.3 | 3705 | Silent Mutation | ATC,ATT | I,I 466 | NP_000351.2 | |
NM_199292.2 | 3705 | Silent Mutation | ATC,ATT | I,I 497 | NP_954986.2 | |
NM_199293.2 | 3705 | Silent Mutation | ATC,ATT | I,I 493 | NP_954987.2 | |
XM_011520335.2 | 3705 | Silent Mutation | ATC,ATT | I,I 470 | XP_011518637.1 |