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GAGCTGCTGCTGGTACTTGTCCTCG[C/T]ACTGCTCCGCGACCCTGAGCTGACC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602466 | ||||||||||||||||||||
Literature Links: |
SPRY2 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 |
SPRY2 - sprouty RTK signaling antagonist 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318536.1 | 909 | Missense Mutation | ACG,GCG | T,A 122 | NP_001305465.1 | |
NM_001318537.1 | 909 | Missense Mutation | ACG,GCG | T,A 122 | NP_001305466.1 | |
NM_001318538.1 | 909 | Missense Mutation | ACG,GCG | T,A 122 | NP_001305467.1 | |
NM_005842.3 | 909 | Missense Mutation | ACG,GCG | T,A 122 | NP_005833.1 |