MIR6886, microRNA 6886, 102465534
N. diseases: 6; N. variants: 286
Source: ALL
Variant | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Disease | Disease Class | Score vda | EI vda | N. PMIDs | First Ref. | Last Ref. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
0.882 | 0.120 | 19 | 11111523 | frameshift variant | A/- | del |
|
0.700 | 0 | ||||||||||||
|
0.925 | 0.120 | 19 | 11113262 | coding sequence variant | -/GGACCCCCAGGCTCCATCGCCTACCTCTTCTTCACCAACCGGCACGAGGTCAGGAAGATGACGCTGGACCGGAGCGAGTACACCAGCCTCATCCCC | delins |
|
0.700 | 0 | ||||||||||||
|
0.807 | 0.120 | 19 | 11113451 | splice donor variant | T/A;C | snv |
|
0.700 | 0 | ||||||||||||
|
0.827 | 0.080 | 19 | 11113376 | missense variant | G/A;C;T | snv | 1.2E-05 |
|
0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 19 | 11113382 | missense variant | G/A;C;T | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.807 | 0.200 | 19 | 11113743 | missense variant | G/A;C;T | snv | 1.2E-05; 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 19 | 11113329 | missense variant | C/T | snv | 2.8E-05 | 7.0E-06 |
|
0.700 | 0 | ||||||||||
|
1.000 | 0.080 | 19 | 11113679 | synonymous variant | G/A | snv | 3.2E-05 | 7.7E-05 |
|
0.700 | 0 | ||||||||||
|
0.882 | 0.160 | 19 | 11113650 | missense variant | G/A;C | snv | 2.4E-05; 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 19 | 11113308 | missense variant | G/A;C | snv | 1.6E-05 |
|
0.700 | 0 | |||||||||||
|
0.827 | 0.200 | 19 | 11113337 | missense variant | C/T | snv | 2.4E-05 | 7.0E-06 |
|
0.700 | 0 | ||||||||||
|
0.925 | 0.080 | 19 | 11113414 | missense variant | C/G;T | snv | 3.2E-04 |
|
0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 19 | 11111586 | missense variant | A/C | snv | 8.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.827 | 0.120 | 19 | 11113590 | missense variant | G/A;T | snv | 5.6E-05 | 2.1E-05 |
|
0.700 | 0 | ||||||||||
|
0.925 | 0.080 | 19 | 11113686 | stop gained | A/G;T | snv | 1.2E-05 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.080 | 19 | 11113752 | missense variant | C/A;T | snv | 8.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 19 | 11113392 | missense variant | C/A;G;T | snv | 4.0E-06; 8.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 19 | 11111629 | stop gained | C/A | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 19 | 11113705 | missense variant | C/T | snv | 1.6E-05 |
|
0.700 | 0 | |||||||||||
|
0.851 | 0.160 | 19 | 11111514 | missense variant | A/C;G;T | snv | 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
1.000 | 0.080 | 19 | 11113678 | missense variant | C/A;T | snv | 8.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 19 | 11113268 | intron variant | G/A;C | snv | 2.8E-05; 4.0E-06 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 19 | 11111519 | missense variant | G/A;C;T | snv | 1.2E-05 |
|
0.700 | 0 | |||||||||||
|
0.925 | 0.080 | 19 | 11111556 | missense variant | G/A;C | snv | 1.2E-05 |
|
0.700 | 0 | |||||||||||
|
0.882 | 0.160 | 19 | 11113338 | missense variant | G/A;C;T | snv | 1.6E-05 |
|
0.700 | 0 |