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TCGTTGGAGACACTGAAACATACTC[C/T]AGGTTCCTTGCGGACTCTGCTGTTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
4 submissions
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Phenotype: |
MIM: 606446 | ||||||||||||||||||||
Literature Links: |
SLAMF6 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 |
SLAMF6 - SLAM family member 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184714.1 | 886 | Silent Mutation | CTA,CTG | L,L 272 | NP_001171643.1 | |
NM_001184715.1 | 886 | Silent Mutation | CTA,CTG | L,L 222 | NP_001171644.1 | |
NM_001184716.1 | 886 | Silent Mutation | CTA,CTG | L,L 161 | NP_001171645.1 | |
NM_052931.4 | 886 | Silent Mutation | CTA,CTG | L,L 271 | NP_443163.1 | |
XM_017000215.1 | 886 | Silent Mutation | CTA,CTG | L,L 272 | XP_016855704.1 | |
XM_017000216.1 | 886 | Silent Mutation | CTA,CTG | L,L 223 | XP_016855705.1 | |
XM_017000217.1 | 886 | Silent Mutation | CTA,CTG | L,L 160 | XP_016855706.1 |