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CGTTGGAGTCCGACTGGCCTTGGGC[C/T]GAAAGAGGCTGCCCTGCTGGGTGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607217 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SDK2 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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SDK2 - sidekick cell adhesion molecule 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144952.1 | 6383 | Missense Mutation | CAG,CGG | Q,R 2128 | NP_001138424.1 | |
XM_011524914.2 | 6383 | Missense Mutation | CAG,CGG | Q,R 2109 | XP_011523216.1 | |
XM_011524915.2 | 6383 | Intron | XP_011523217.1 | |||
XM_011524916.2 | 6383 | Intron | XP_011523218.1 |