TNRC6B, trinucleotide repeat containing adaptor 6B, 23112
N. diseases: 25; N. variants: 24
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. | ||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1.000 | 22 | 40256869 | intron variant | A/G | snv | 0.19 |
|
Neoplasms | 0.820 | 1.000 | 3 | 2011 | 2018 | ||||||||
|
22 | 40208941 | intron variant | T/A;G | snv |
|
0.700 | 1.000 | 3 | 2015 | 2018 | |||||||||||
|
22 | 40263569 | intron variant | T/C | snv | 0.45 |
|
0.700 | 1.000 | 3 | 2016 | 2017 | ||||||||||
|
22 | 40317857 | intron variant | T/A | snv | 0.69 |
|
0.700 | 1.000 | 2 | 2017 | 2018 | ||||||||||
|
22 | 40196077 | intron variant | TTT/-;T;TT;TTTT;TTTTTTTTT | delins | 0.68 |
|
0.700 | 1.000 | 1 | 2016 | 2016 | ||||||||||
|
1.000 | 0.080 | 22 | 40143521 | intron variant | G/A;C | snv |
|
Neoplasms; Skin and Connective Tissue Diseases | 0.700 | 1.000 | 1 | 2017 | 2017 | ||||||||
|
22 | 40162060 | intron variant | T/C | snv | 0.29 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 22 | 40256869 | intron variant | A/G | snv | 0.19 |
|
0.700 | 1.000 | 1 | 2011 | 2011 | |||||||||
|
1.000 | 22 | 40307071 | intron variant | T/G | snv | 0.20 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 22 | 40307071 | intron variant | T/G | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
22 | 40258272 | intron variant | T/C | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
22 | 40318352 | intron variant | C/G | snv | 4.1E-02 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
22 | 40301577 | intron variant | C/T | snv | 0.74 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
22 | 40301577 | intron variant | C/T | snv | 0.74 |
|
0.700 | 1.000 | 1 | 2009 | 2009 | ||||||||||
|
22 | 40330179 | 3 prime UTR variant | T/C | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 22 | 40315223 | intron variant | -/T | delins | 0.22 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 22 | 40315223 | intron variant | -/T | delins | 0.22 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
22 | 40151561 | intron variant | AAA/-;AA;AAAA;AAAAA;AAAAAA;AAAAAAA;AAAAAAAA;AAAAAAAAA | delins |
|
0.700 | 1.000 | 1 | 2016 | 2016 | |||||||||||
|
22 | 40154103 | intron variant | T/C | snv | 0.68 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 22 | 40158441 | intron variant | A/G;T | snv | 0.17 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2018 | 2018 | ||||||||
|
1.000 | 22 | 40158441 | intron variant | A/G;T | snv | 0.17 |
|
0.700 | 1.000 | 1 | 2018 | 2018 | |||||||||
|
22 | 40294381 | intron variant | A/G | snv | 0.31 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||||
|
1.000 | 22 | 40263247 | intron variant | T/A | snv | 0.20 |
|
Neoplasms | 0.700 | 1.000 | 1 | 2019 | 2019 | ||||||||
|
1.000 | 22 | 40263247 | intron variant | T/A | snv | 0.20 |
|
0.700 | 1.000 | 1 | 2019 | 2019 | |||||||||
|
1.000 | 0.080 | 22 | 40075184 | intron variant | C/T | snv | 0.34 |
|
Neoplasms; Male Urogenital Diseases | 0.700 | 1.000 | 1 | 2018 | 2018 |