Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCAGTAGTTCTCCAGCTGGTAGAGG[G/C]AGCAGATGCTGGTACAGCATTGTTC
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 |
---|---|---|
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 |
INS - insulin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000207.2 | 387 | Missense Mutation | TCC,TGC | S,C 101 | NP_000198.1 | |
NM_001185097.1 | 387 | Missense Mutation | TCC,TGC | S,C 101 | NP_001172026.1 | |
NM_001185098.1 | 387 | Missense Mutation | TCC,TGC | S,C 101 | NP_001172027.1 | |
NM_001291897.1 | 387 | Missense Mutation | TCC,TGC | S,C 101 | NP_001278826.1 |
INS-IGF2 - INS-IGF2 readthrough | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001042376.2 | 387 | Intron | NP_001035835.1 |
TH - tyrosine hydroxylase | ||||||
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There are no transcripts associated with this gene. |