regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
WWOX_chr16_78094654_79217667 | 78751415 | T | TTA | intron_variant | MODIFIER | HG00738.hp1 HG01891.hp1 HG02109.hp1 others(12): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0007a0002c0002others(8): Show | a0001c0001t0027a0001c0007t0008a0002c0002t0007others(12): Show | a0001c0001t0027g0096a0001c0007t0008g0108a0002c0002t0007g0047others(12): Show | 15 | 142 | 0.1056 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78751461 | T | TTA | intron_variant | MODIFIER | HG00558.hp1 HG00609.hp2 HG00738.hp2 others(30): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0019a0002c0002others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0042others(30): Show | 33 | 142 | 0.2324 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78756320 | C | CCA | intron_variant | MODIFIER | HG02109.hp1 HG02723.hp2 HG02809.hp1 others(6): Show |
a0001a0002a0005others(3): Show | a0001c0007a0002c0002a0005c0005others(4): Show | a0001c0007t0008a0002c0002t0007a0005c0005t0024others(6): Show | a0001c0007t0008g0108a0002c0002t0007g0047a0005c0005t0024g0112others(6): Show | 9 | 142 | 0.0634 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78767482 | C | CTG | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00741.hp1 others(34): Show |
a0001a0002a0003others(6): Show | a0001c0001a0002c0002a0003c0004others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0042others(34): Show | 37 | 142 | 0.2606 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78774496 | T | TTG | intron_variant | MODIFIER | HG01891.hp1 HG02818.hp1 HG02965.hp1 others(1): Show |
a0001a0005a0007others(1): Show | a0001c0001a0005c0005a0007c0008others(1): Show | a0001c0001t0027a0005c0005t0003a0007c0008t0026others(1): Show | a0001c0001t0027g0096a0005c0005t0003g0107a0007c0008t0026g0040others(1): Show | 4 | 142 | 0.0282 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78791018 | C | CAA | intron_variant | MODIFIER | HG00438.hp1 HG00738.hp1 HG00741.hp1 others(40): Show |
a0001a0002a0003others(8): Show | a0001c0001a0002c0002a0002c0022others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | a0001c0001t0001g0021a0001c0001t0001g0025a0001c0001t0001g0026others(40): Show | 43 | 142 | 0.3028 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78796827 | C | CTT | intron_variant | MODIFIER | HG01884.hp1 HG02257.hp1 HG03453.hp2 others(3): Show |
a0001a0004a0012 | a0001c0001a0004c0006a0012c0016 | a0001c0001t0004a0001c0001t0021a0004c0006t0001others(1): Show | a0001c0001t0004g0004a0001c0001t0004g0053a0001c0001t0004g0084others(3): Show | 6 | 142 | 0.0423 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78798591 | G | GTT | intron_variant | MODIFIER | HG00438.hp2 HG02109.hp2 HG02486.hp2 others(9): Show |
a0001a0003a0004others(3): Show | a0001c0001a0001c0007a0003c0004others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0007t0007others(8): Show | a0001c0001t0001g0085a0001c0001t0001g0142a0001c0001t0003g0073others(9): Show | 12 | 142 | 0.0845 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78798593 | T | TTG | intron_variant | MODIFIER | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(34): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0007a0002c0002others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0022others(34): Show | 37 | 142 | 0.2606 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78805427 | A | ATT | intron_variant | MODIFIER | HG00738.hp1 HG01109.hp2 HG01891.hp2 others(4): Show |
a0001a0003a0006others(1): Show | a0001c0001a0003c0004a0003c0017others(2): Show | a0001c0001t0001a0001c0001t0002a0003c0004t0001others(4): Show | a0001c0001t0001g0137a0001c0001t0002g0015a0003c0004t0001g0036others(4): Show | 7 | 142 | 0.0493 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78817172 | C | CTT | intron_variant | MODIFIER | HG01257.hp2 HG02257.hp1 HG02818.hp2 others(2): Show |
a0001a0004a0010 | a0001c0001a0001c0007a0004c0006others(1): Show | a0001c0001t0001a0001c0001t0021a0001c0007t0007others(2): Show | a0001c0001t0001g0024a0001c0001t0021g0006a0001c0007t0007g0111others(2): Show | 5 | 142 | 0.0352 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78823781 | A | ATT | intron_variant | MODIFIER | HG00741.hp1 HG03041.hp2 HG03490.hp2 others(6): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(4): Show | a0001c0001t0001g0137a0001c0001t0002g0032a0001c0001t0002g0052others(6): Show | 9 | 142 | 0.0634 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78827676 | T | TAC | intron_variant | MODIFIER | HG01257.hp1 HG01258.hp2 HG02818.hp1 others(7): Show |
a0001a0002a0004others(3): Show | a0001c0001a0002c0002a0004c0006others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(6): Show | a0001c0001t0001g0033a0001c0001t0003g0060a0001c0001t0003g0106others(7): Show | 10 | 142 | 0.0704 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78830310 | T | TTA | intron_variant | MODIFIER | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(41): Show |
a0001a0002a0004others(5): Show | a0001c0001a0001c0007a0001c0019others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0029others(41): Show | 44 | 142 | 0.3099 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78840813 | A | ATC | intron_variant | MODIFIER | HG02723.hp1 HG03710.hp2 |
a0001a0005 | a0001c0001a0005c0005 | a0001c0001t0003a0005c0005t0002 | a0001c0001t0003g0076a0005c0005t0002g0009 | 2 | 142 | 0.0141 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78849573 | C | CAA | intron_variant | MODIFIER | HG00609.hp1 HG01074.hp2 HG01081.hp2 others(27): Show |
a0001a0002a0012others(3): Show | a0001c0001a0001c0007a0001c0019others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(27): Show | 30 | 142 | 0.2113 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78858144 | T | TTG | intron_variant | MODIFIER | HG00735.hp1 HG00741.hp1 HG03490.hp2 others(5): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0002a0004c0006others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0022a0001c0001t0002g0052a0001c0001t0002g0056others(5): Show | 8 | 142 | 0.0563 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78858330 | A | ATG | intron_variant | MODIFIER | HG00438.hp2 HG00558.hp1 HG00735.hp2 others(49): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0007a0002c0002others(13): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(28): Show | a0001c0001t0001g0029a0001c0001t0001g0119a0001c0001t0001g0120others(49): Show | 52 | 142 | 0.3662 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78859050 | G | GTA | intron_variant | MODIFIER | HG02572.hp2 HG02809.hp1 HG03098.hp1 others(4): Show |
a0001a0002a0005others(2): Show | a0001c0001a0002c0002a0005c0005others(2): Show | a0001c0001t0001a0001c0001t0005a0002c0002t0001others(4): Show | a0001c0001t0001g0002a0001c0001t0005g0034a0002c0002t0001g0138others(4): Show | 7 | 142 | 0.0493 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78867484 | T | TTG | intron_variant | MODIFIER | HG00558.hp1 HG01071.hp2 HG01074.hp1 others(23): Show |
a0001a0002a0005others(3): Show | a0001c0001a0002c0002a0002c0022others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0024others(23): Show | 26 | 142 | 0.1831 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78874255 | C | CAA | intron_variant | MODIFIER | HG01109.hp2 HG02109.hp2 HG02145.hp2 others(9): Show |
a0001a0002a0003others(5): Show | a0001c0001a0002c0002a0002c0022others(7): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(8): Show | a0001c0001t0001g0085a0001c0001t0002g0015a0002c0002t0001g0010others(9): Show | 12 | 142 | 0.0845 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78874684 | C | CTT | intron_variant | MODIFIER | HG00558.hp2 HG00741.hp2 HG01071.hp1 others(28): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0019a0002c0002others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0023others(28): Show | 31 | 142 | 0.2183 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78878901 | G | GAA | intron_variant | MODIFIER | HG00558.hp1 HG00609.hp1 HG01081.hp1 others(21): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0004others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0029a0001c0001t0001g0119a0001c0001t0001g0120others(21): Show | 24 | 142 | 0.1690 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78879877 | C | CAA | intron_variant | MODIFIER | HG02257.hp1 HG02486.hp1 HG02572.hp1 others(6): Show |
a0001a0002a0004others(3): Show | a0001c0001a0002c0022a0004c0006others(4): Show | a0001c0001t0001a0001c0001t0017a0001c0001t0021others(6): Show | a0001c0001t0001g0003a0001c0001t0017g0103a0001c0001t0021g0006others(6): Show | 9 | 142 | 0.0634 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78884273 | C | CAA | intron_variant | MODIFIER | HG01496.hp2 HG02015.hp2 NA18747.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(1): Show | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0003g0065others(3): Show | 6 | 142 | 0.0423 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78886639 | C | CAT | intron_variant | MODIFIER | HG01081.hp1 HG01192.hp2 HG01257.hp1 others(19): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0007a0002c0002others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0012a0001c0001t0002g0052a0001c0001t0003g0075others(19): Show | 22 | 142 | 0.1549 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78887077 | G | GGT | intron_variant | MODIFIER | HG01192.hp2 HG01891.hp1 HG02257.hp1 others(5): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0007a0002c0002others(3): Show | a0001c0001t0021a0001c0001t0027a0001c0007t0008others(5): Show | a0001c0001t0021g0006a0001c0001t0027g0096a0001c0007t0008g0108others(5): Show | 8 | 142 | 0.0563 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78887518 | C | CAT | intron_variant | MODIFIER | HG01109.hp2 HG02809.hp2 HG03579.hp2 others(2): Show |
a0001a0003a0005others(2): Show | a0001c0001a0003c0004a0005c0005others(2): Show | a0001c0001t0002a0003c0004t0004a0005c0005t0003others(2): Show | a0001c0001t0002g0015a0003c0004t0004g0013a0005c0005t0003g0061others(2): Show | 5 | 142 | 0.0352 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78897240 | T | TAA | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(15): Show |
a0001a0002a0005others(2): Show | a0001c0001a0002c0002a0005c0005others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0049others(15): Show | 18 | 142 | 0.1268 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78908541 | G | GAA | intron_variant | MODIFIER | HG00438.hp1 HG00735.hp1 HG00735.hp2 others(44): Show |
a0001a0002a0003others(7): Show | a0001c0001a0002c0002a0003c0004others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(44): Show | 47 | 142 | 0.3310 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78910158 | T | TCC | intron_variant | MODIFIER | HG00558.hp1 HG00738.hp2 HG01192.hp1 others(13): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0029a0001c0001t0001g0139a0001c0001t0002g0032others(13): Show | 16 | 142 | 0.1127 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78923794 | G | GTT | intron_variant | MODIFIER | HG00609.hp2 HG01074.hp2 HG01192.hp1 others(10): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0007a0002c0002others(5): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(9): Show | a0001c0001t0001g0022a0001c0001t0001g0042a0001c0001t0004g0121others(10): Show | 13 | 142 | 0.0916 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78930274 | T | TTC | intron_variant | MODIFIER | HG02145.hp2 HG02559.hp1 HG03579.hp2 others(1): Show |
a0001a0003a0014 | a0001c0001a0003c0004a0014c0014 | a0001c0001t0004a0003c0004t0001a0003c0004t0004others(1): Show | a0001c0001t0004g0084a0003c0004t0001g0097a0003c0004t0004g0013others(1): Show | 4 | 142 | 0.0282 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78930448 | A | ATT | intron_variant | MODIFIER | HG01884.hp2 HG02258.hp1 HG02886.hp1 others(4): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0019a0003c0004others(2): Show | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(4): Show | a0001c0001t0003g0075a0001c0001t0006g0078a0001c0001t0008g0086others(4): Show | 7 | 142 | 0.0493 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78934508 | C | CAA | intron_variant | MODIFIER | HG02572.hp1 HG02723.hp2 HG02886.hp2 others(3): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0007a0003c0017others(2): Show | a0001c0001t0001a0001c0007t0007a0001c0007t0008others(3): Show | a0001c0001t0001g0049a0001c0007t0007g0111a0001c0007t0008g0108others(3): Show | 6 | 142 | 0.0423 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78937448 | C | CTT | intron_variant | MODIFIER | HG01081.hp1 HG01258.hp2 HG02257.hp1 others(3): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0019a0002c0002others(3): Show | a0001c0001t0021a0001c0019t0005a0002c0002t0001others(3): Show | a0001c0001t0021g0006a0001c0019t0005g0123a0002c0002t0001g0092others(3): Show | 6 | 142 | 0.0423 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78950533 | T | TAC | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(49): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0007a0001c0019others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0024others(49): Show | 52 | 142 | 0.3662 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78962302 | C | CTT | intron_variant | MODIFIER | HG00438.hp2 HG01071.hp1 HG01071.hp2 others(11): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0007a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(6): Show | a0001c0001t0001g0093a0001c0001t0001g0120a0001c0001t0003g0062others(11): Show | 14 | 142 | 0.0986 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78967286 | C | CTT | intron_variant | MODIFIER | HG00558.hp1 HG00609.hp2 HG00738.hp1 others(22): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0007a0001c0019others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0042others(22): Show | 25 | 142 | 0.1761 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78967458 | G | GTT | intron_variant | MODIFIER | HG02145.hp2 HG02257.hp2 |
a0001a0014 | a0001c0001a0014c0014 | a0001c0001t0005a0014c0014t0004 | a0001c0001t0005g0095a0014c0014t0004g0133 | 2 | 142 | 0.0141 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78967459 | G | GTT | intron_variant | MODIFIER | HG00438.hp1 HG00558.hp2 HG01258.hp1 others(17): Show |
a0001a0002a0004others(5): Show | a0001c0001a0002c0002a0004c0006others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(9): Show | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0025others(17): Show | 20 | 142 | 0.1409 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78979084 | C | CTT | intron_variant | MODIFIER | HG01081.hp1 HG02109.hp1 HG02257.hp1 others(7): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0002c0022others(4): Show | a0001c0001t0017a0001c0001t0021a0002c0002t0001others(6): Show | a0001c0001t0017g0103a0001c0001t0021g0006a0002c0002t0001g0010others(7): Show | 10 | 142 | 0.0704 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78983870 | C | CTT | intron_variant | MODIFIER | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(41): Show |
a0001a0002a0004others(6): Show | a0001c0001a0001c0019a0002c0002others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0029others(41): Show | 44 | 142 | 0.3099 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78989821 | C | CGT | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(25): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0007a0001c0019others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0093a0001c0001t0001g0120a0001c0001t0001g0126others(25): Show | 28 | 142 | 0.1972 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78989826 | G | GTT | intron_variant | MODIFIER | HG01884.hp2 HG02559.hp2 HG02630.hp2 others(3): Show |
a0001a0003a0007others(1): Show | a0001c0001a0001c0007a0003c0004others(2): Show | a0001c0001t0001a0001c0007t0007a0001c0007t0008others(3): Show | a0001c0001t0001g0012a0001c0007t0007g0111a0001c0007t0008g0108others(3): Show | 6 | 142 | 0.0423 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78992953 | T | TAA | intron_variant | MODIFIER | HG02109.hp2 HG02965.hp1 HG03453.hp1 others(2): Show |
a0001a0004a0008 | a0001c0001a0004c0006a0008c0024 | a0001c0001t0001a0004c0006t0004a0008c0024t0003 | a0001c0001t0001g0085a0001c0001t0001g0093a0001c0001t0001g0119others(2): Show | 5 | 142 | 0.0352 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78994969 | C | CTT | intron_variant | MODIFIER | HG00609.hp2 HG00741.hp1 HG00741.hp2 others(16): Show |
a0001a0002a0005others(3): Show | a0001c0001a0002c0002a0005c0005others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(10): Show | a0001c0001t0001g0021a0001c0001t0001g0042a0001c0001t0001g0049others(16): Show | 19 | 142 | 0.1338 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78996151 | A | ATT | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG00738.hp1 others(15): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0003a0001c0001t0001g0033a0001c0001t0002g0044others(15): Show | 18 | 142 | 0.1268 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78996376 | A | ACC | intron_variant | MODIFIER | HG00609.hp1 HG01074.hp2 HG01109.hp1 others(17): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0004others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0021a0001c0001t0001g0093a0001c0001t0001g0120others(17): Show | 20 | 142 | 0.1409 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 79002213 | C | CTT | intron_variant | MODIFIER | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(6): Show |
a0001a0002a0008 | a0001c0001a0002c0002a0008c0024 | a0001c0001t0001a0001c0001t0008a0001c0001t0021others(4): Show | a0001c0001t0001g0085a0001c0001t0001g0093a0001c0001t0008g0086others(6): Show | 9 | 142 | 0.0634 | 2 | c.105 others(25): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar |