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)