Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCCGAAGCCCGTGATGTCAGTGGC[A/G]GCGTGGGCATTGAACGTGTGCATGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600902 | ||||||||||||||||||||
Literature Links: |
SEPHS1 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 |
SEPHS1 - selenophosphate synthetase 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001195602.1 | 1152 | Intron | NP_001182531.1 | |||
NM_001195604.1 | 1152 | Intron | NP_001182533.1 | |||
NM_012247.4 | 1152 | Intron | NP_036379.2 | |||
XM_017015942.1 | 1152 | Silent Mutation | GCC,GCT | A,A 262 | XP_016871431.1 | |
XM_017015943.1 | 1152 | Silent Mutation | GCC,GCT | A,A 262 | XP_016871432.1 | |
XM_017015944.1 | 1152 | Silent Mutation | GCC,GCT | A,A 260 | XP_016871433.1 | |
XM_017015945.1 | 1152 | Intron | XP_016871434.1 |