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- SNP ID:
- rs137954605
- Gene
-
CXCL16MED11ZMYND15 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.17: 4735292 - 4735292 on Build GRCh38
- Polymorphism:
- G/T, Transversion substitution
- Context Sequence [VIC/FAM]:
AGCTGCCAGACTGTGGCCCGCAGTG[G/T]GAATGGTGGTTTCATTGGGACGAGT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605398
MIM: 612383
MIM: 614312
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Literature Links: |
CXCL16 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
|
| CXCL16 - C-X-C motif chemokine ligand 16 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001100812.1 | 1107 | Missense Mutation | CAC,CCC | H,P 192 | NP_001094282.1 | |
| NM_022059.3 | 1107 | Missense Mutation | CAC,CCC | H,P 192 | NP_071342.2 | |
| MED11 - mediator complex subunit 11 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| ZMYND15 - zinc finger MYND-type containing 15 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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