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Search Thermo Fisher Scientific
CATCATGGAACCCAAACCTCAGAAG[A/G]GTCCAGGTACCCGAGGGGTATAATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
PLEKHS1 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 |
PLEKHS1 - pleckstrin homology domain containing S1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001193434.1 | 349 | UTR 5 | NP_001180363.1 | |||
NM_001193435.1 | 349 | UTR 5 | NP_001180364.1 | |||
NM_024889.4 | 349 | Missense Mutation | AGT,GGT | S,G 8 | NP_079165.3 | |
NM_182601.1 | 349 | Intron | NP_872407.1 | |||
XM_005270162.2 | 349 | Missense Mutation | AGT,GGT | S,G 8 | XP_005270219.1 | |
XM_005270163.2 | 349 | Missense Mutation | AGT,GGT | S,G 8 | XP_005270220.1 | |
XM_011540171.1 | 349 | Missense Mutation | AGT,GGT | S,G 8 | XP_011538473.1 | |
XM_011540172.1 | 349 | Missense Mutation | AGT,GGT | S,G 8 | XP_011538474.1 | |
XM_011540173.1 | 349 | Missense Mutation | AGT,GGT | S,G 8 | XP_011538475.1 | |
XM_011540174.2 | 349 | Missense Mutation | AGT,GGT | S,G 8 | XP_011538476.1 | |
XM_011540175.1 | 349 | UTR 5 | XP_011538477.1 | |||
XM_011540176.1 | 349 | UTR 5 | XP_011538478.1 | |||
XM_017016666.1 | 349 | Missense Mutation | AGT,GGT | S,G 8 | XP_016872155.1 |