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TTTTCTCTTTGTTCTTATTTTCTCC[A/G]CTTGCTGAATATCTGTTTTAGAGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 147440 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IGF1 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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IGF1 - insulin like growth factor 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000618.4 | 4635 | UTR 3 | NP_000609.1 | |||
NM_001111283.2 | 4635 | UTR 3 | NP_001104753.1 | |||
NM_001111284.1 | 4635 | UTR 3 | NP_001104754.1 | |||
XM_017019259.1 | 4635 | Intron | XP_016874748.1 | |||
XM_017019260.1 | 4635 | Intron | XP_016874749.1 | |||
XM_017019261.1 | 4635 | Intron | XP_016874750.1 | |||
XM_017019262.1 | 4635 | UTR 3 | XP_016874751.1 | |||
XM_017019263.1 | 4635 | UTR 3 | XP_016874752.1 |