Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATATCACCCACTTTCCAGGACTTCC[A/G]ATGAACCAGCTGCACGACATCTAGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611646 | ||||||||||||||||||||
Literature Links: |
SPHKAP 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 |
SPHKAP - SPHK1 interactor, AKAP domain containing | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142644.1 | 5585 | Missense Mutation | CGG,TGG | R,W 1663 | NP_001136116.1 | |
NM_030623.3 | 5585 | Missense Mutation | CGG,TGG | R,W 1634 | NP_085126.2 | |
XM_005246870.4 | 5585 | Missense Mutation | CGG,TGG | R,W 1646 | XP_005246927.1 | |
XM_006712777.3 | 5585 | Missense Mutation | CGG,TGG | R,W 1688 | XP_006712840.1 | |
XM_006712778.3 | 5585 | Missense Mutation | CGG,TGG | R,W 1659 | XP_006712841.1 | |
XM_011511925.2 | 5585 | Missense Mutation | CGG,TGG | R,W 1678 | XP_011510227.1 |