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GGAAATCCAGAATCATTGCAAAAAA[C/T]GTATCTACCTCCAAACCTGAGTTTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607693 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SECISBP2 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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SECISBP2 - SECIS binding protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282688.1 | 782 | Silent Mutation | AAC,AAT | N,N 207 | NP_001269617.1 | |
NM_001282689.1 | 782 | Silent Mutation | AAC,AAT | N,N 135 | NP_001269618.1 | |
NM_001282690.1 | 782 | Silent Mutation | AAC,AAT | N,N 140 | NP_001269619.1 | |
NM_024077.4 | 782 | Silent Mutation | AAC,AAT | N,N 208 | NP_076982.3 | |
XM_005252196.2 | 782 | Silent Mutation | AAC,AAT | N,N 208 | XP_005252253.1 | |
XM_005252202.3 | 782 | Intron | XP_005252259.1 | |||
XM_006717282.2 | 782 | Silent Mutation | AAC,AAT | N,N 135 | XP_006717345.1 | |
XM_011519000.2 | 782 | Silent Mutation | AAC,AAT | N,N 140 | XP_011517302.1 | |
XM_011519001.1 | 782 | Silent Mutation | AAC,AAT | N,N 140 | XP_011517303.1 | |
XM_011519002.1 | 782 | Silent Mutation | AAC,AAT | N,N 140 | XP_011517304.1 | |
XM_011519003.1 | 782 | Silent Mutation | AAC,AAT | N,N 140 | XP_011517305.1 | |
XM_017015122.1 | 782 | Silent Mutation | AAC,AAT | N,N 208 | XP_016870611.1 | |
XM_017015123.1 | 782 | Silent Mutation | AAC,AAT | N,N 208 | XP_016870612.1 | |
XM_017015124.1 | 782 | Silent Mutation | AAC,AAT | N,N 208 | XP_016870613.1 | |
XM_017015125.1 | 782 | UTR 5 | XP_016870614.1 |