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ATGACCCCCTTCTTCCAGGAAGCGC[C/T]TCTTGGACGCGTGTGACCGATGCCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 602055 | ||||||||||||||||||||
Literature Links: |
INSIG1 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 |
INSIG1 - insulin induced gene 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005542.4 | 192 | UTR 5 | NP_005533.2 | |||
NM_198336.2 | 192 | UTR 5 | NP_938150.2 | |||
NM_198337.2 | 192 | UTR 5 | NP_938151.1 | |||
XM_005249542.1 | 192 | UTR 5 | XP_005249599.1 | |||
XM_005249543.1 | 192 | UTR 5 | XP_005249600.1 | |||
XM_017012177.1 | 192 | UTR 5 | XP_016867666.1 |