SNP Report

Basic Info
| Name |
rs28358884
dbSNP
Ensembl
|
| Location |
MT:8414 - 8414(+) |
| Variant Seq |
T |
| Ancestral Allele |
C |
| Ref Seq |
C |
| Annotation |
downstream_gene_variant; missense_variant; upstream_gene_variant
|
| Variant Effect |
downstream_gene_variant(ENST00000387382, ENST00000387377, ENST00000361739, ENST00000361390, ENST00000361453, ENST00000387421, ENST00000387365, ENST00000361624, ENST00000387419); missense_variant(ENST00000361851); upstream_gene_variant(ENST00000361567, ENST00000361227, ENST00000361381, ENST00000387405, ENST00000387449, ENST00000387429, ENST00000387400, ENST00000387372, ENST00000387416, ENST00000361335, ENST00000387409, ENST00000387392, ENST00000387441, ENST00000362079, ENST00000387456, ENST00000361899, ENST00000387439)
|
| SIFT Annotation |
tolerated
|
| SIFT Variant Effect |
tolerated(ENST00000361851)
|
| PolyPhen Annotation |
probably_damaging
|
| PolyPhen Variant Effect |
probably_damaging(ENST00000361851)
|
| rSNP? |
No
Link in rVarBase
|
| Related Regulatory Elements |
N.A.
|
| Chromatin State |
N.A.
|
| No. of Marker's Association Results |
1 (Positive: 0; Negative: 0; Trend: 1) |
| Source |
Literature |

SNP related association results

SNP related genes (count: 27)

SNPs in LD with rs28358884 (count: 0)

SNP related eQTL (count: 1)