Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCGGCAGCTGGAGGCCCAGATCAGA[A/G]GGCTACCCCAGGACCCTGCCCTTTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605398 MIM: 612383 MIM: 614312 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CXCL16 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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CXCL16 - C-X-C motif chemokine ligand 16 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001100812.1 | 211 | Intron | NP_001094282.1 | |||
NM_022059.3 | 211 | Intron | NP_071342.2 |
MED11 - mediator complex subunit 11 | ||||||
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There are no transcripts associated with this gene. |
ZMYND15 - zinc finger MYND-type containing 15 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136046.2 | 211 | Missense Mutation | AGG,GGG | R,G 49 | NP_001129518.1 | |
NM_001267822.1 | 211 | Missense Mutation | AGG,GGG | R,G 49 | NP_001254751.1 | |
NM_032265.2 | 211 | Missense Mutation | AGG,GGG | R,G 49 | NP_115641.1 | |
XM_017025218.1 | 211 | Missense Mutation | AGG,GGG | R,G 49 | XP_016880707.1 |