Search Thermo Fisher Scientific
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ATCCAGTCGACTGATACCCTTCTTG[A/G]AGGTCGCCTGAAACTAAGAGTAAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
IWS1 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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IWS1 - IWS1, SUPT6H interacting protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017969.2 | 2806 | Missense Mutation | TCC,TTC | S,F 781 | NP_060439.2 | |
XM_005263707.3 | 2806 | Missense Mutation | TCC,TTC | S,F 786 | XP_005263764.1 | |
XM_006712626.3 | 2806 | UTR 3 | XP_006712689.1 | |||
XM_011511450.1 | 2806 | Intron | XP_011509752.1 | |||
XM_011511452.1 | 2806 | Intron | XP_011509754.1 | |||
XM_017004467.1 | 2806 | UTR 3 | XP_016859956.1 | |||
XM_017004468.1 | 2806 | Missense Mutation | TCC,TTC | S,F 574 | XP_016859957.1 |