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 | 78106411 | G | GTT | intron_variant | MODIFIER | HG00735.hp1 HG00738.hp2 HG01071.hp2 others(9): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0004 | a0001c0001t0003a0001c0001t0006a0001c0001t0012others(5): Show | a0001c0001t0003g0060a0001c0001t0003g0062a0001c0001t0003g0075others(9): Show | 12 | 142 | 0.0845 | 2 | c.108 others(19): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78107611 | T | TGC | intron_variant | MODIFIER | HG01081.hp1 HG01109.hp2 HG01891.hp1 others(12): Show |
a0001a0003a0004others(4): Show | a0001c0001a0003c0004a0004c0006others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(11): Show | a0001c0001t0001g0012a0001c0001t0002g0015a0001c0001t0004g0113others(12): Show | 15 | 142 | 0.1056 | 2 | c.108 others(17): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 1/8 | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78124861 | C | CTT | intron_variant | MODIFIER | HG02559.hp1 NA19030.hp1 |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0017a0003c0004t0001 | a0001c0001t0017g0103a0003c0004t0001g0097 | 2 | 142 | 0.0141 | 2 | c.409 others(19): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78127516 | G | GAA | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(21): Show |
a0001a0002a0004others(2): Show | a0001c0001a0002c0002a0004c0006others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(8): Show | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0021others(21): Show | 24 | 142 | 0.1690 | 2 | c.409 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78141430 | C | CTT | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(14): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(5): Show | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0003g0062others(14): Show | 17 | 142 | 0.1197 | 2 | c.410 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78143752 | G | GTT | intron_variant | MODIFIER | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(41): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0007a0002c0002others(6): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(23): Show | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(41): Show | 44 | 142 | 0.3099 | 2 | c.410 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78144445 | A | ACG | intron_variant | MODIFIER | HG03453.hp2 HG03710.hp2 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004 | a0001c0001t0003g0076a0001c0001t0004g0053 | 2 | 142 | 0.0141 | 2 | c.410 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 4/8 | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78144448 | C | CGT | intron_variant | MODIFIER | HG01884.hp1 HG02559.hp2 HG02818.hp2 others(2): Show |
a0001a0003a0010others(2): Show | a0001c0001a0003c0004a0010c0025others(2): Show | a0001c0001t0001a0003c0004t0004a0010c0025t0001others(2): Show | a0001c0001t0001g0012a0003c0004t0004g0013a0010c0025t0001g0007others(2): Show | 5 | 142 | 0.0352 | 2 | c.410 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 4/8 | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78144473 | A | ACG | intron_variant | MODIFIER | HG01496.hp1 HG02083.hp2 HG02630.hp1 others(1): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0002a0004c0023others(1): Show | a0001c0001t0001a0002c0002t0002a0004c0023t0001others(1): Show | a0001c0001t0001g0140a0002c0002t0002g0099a0004c0023t0001g0001others(1): Show | 4 | 142 | 0.0282 | 2 | c.410 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 4/8 | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78148897 | C | CAA | intron_variant | MODIFIER | HG01952.hp1 HG02135.hp1 HG02135.hp2 others(5): Show |
a0001a0002a0015 | a0001c0001a0002c0002a0015c0013 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(3): Show | a0001c0001t0001g0049a0001c0001t0001g0093a0001c0001t0001g0134others(5): Show | 8 | 142 | 0.0563 | 2 | c.410 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78151043 | A | ATT | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(78): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0007a0001c0019others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0024others(78): Show | 81 | 142 | 0.5704 | 2 | c.410 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78152904 | G | GTT | intron_variant | MODIFIER | HG00438.hp2 HG00558.hp1 HG00558.hp2 others(78): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0007a0002c0002others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(41): Show | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0021others(78): Show | 81 | 142 | 0.5704 | 2 | c.410 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78159671 | G | GTT | intron_variant | MODIFIER | HG03486.hp1 NA19030.hp1 |
a0001a0004 | a0001c0001a0004c0006 | a0001c0001t0017a0004c0006t0001 | a0001c0001t0017g0103a0004c0006t0001g0130 | 2 | 142 | 0.0141 | 2 | c.410 others(19): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 4/8 | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78159672 | G | GTT | intron_variant | MODIFIER | HG00438.hp1 HG00735.hp2 HG01891.hp1 others(8): Show |
a0001a0002a0006others(2): Show | a0001c0001a0002c0002a0006c0003others(2): Show | a0001c0001t0001a0001c0001t0025a0001c0001t0027others(5): Show | a0001c0001t0001g0022a0001c0001t0001g0126a0001c0001t0001g0139others(8): Show | 11 | 142 | 0.0775 | 2 | c.410 others(19): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78162472 | A | AAT | intron_variant | MODIFIER | HG00558.hp1 HG00738.hp1 HG00741.hp1 others(44): Show |
a0001a0002a0003others(11): Show | a0001c0001a0002c0002a0003c0004others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0026others(44): Show | 47 | 142 | 0.3310 | 2 | c.410 others(19): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78162514 | G | GCA | intron_variant | MODIFIER | HG00558.hp1 HG00738.hp1 HG00741.hp1 others(41): Show |
a0001a0002a0003others(9): Show | a0001c0001a0002c0002a0003c0004others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0026others(41): Show | 44 | 142 | 0.3099 | 2 | c.410 others(19): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78173958 | T | TGA | intron_variant | MODIFIER | HG01257.hp1 HG01258.hp2 HG01496.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0021a0002c0002t0001others(1): Show | a0001c0001t0003g0106a0001c0001t0021g0006a0002c0002t0001g0092others(1): Show | 4 | 142 | 0.0282 | 2 | c.516 others(19): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78173959 | G | GAA | intron_variant | MODIFIER | HG00558.hp1 HG00741.hp1 HG01496.hp2 others(10): Show |
a0001a0002a0009 | a0001c0001a0002c0002a0009c0010 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0021a0001c0001t0001g0026a0001c0001t0001g0029others(10): Show | 13 | 142 | 0.0916 | 2 | c.516 others(19): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78192491 | C | CAA | intron_variant | MODIFIER | HG00438.hp1 HG00741.hp2 HG01258.hp2 others(31): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0007a0001c0019others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | a0001c0001t0001g0002a0001c0001t0001g0085a0001c0001t0001g0093others(31): Show | 34 | 142 | 0.2394 | 2 | c.516 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78194587 | C | CAA | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(28): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0019a0002c0002others(6): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(14): Show | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0024others(28): Show | 31 | 142 | 0.2183 | 2 | c.516 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78195821 | C | CAA | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(14): Show |
a0001a0002a0010 | a0001c0001a0002c0002a0010c0025 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(5): Show | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(14): Show | 17 | 142 | 0.1197 | 2 | c.516 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78195840 | A | AAG | intron_variant | MODIFIER | HG00438.hp1 HG00735.hp2 HG01891.hp1 others(7): Show |
a0001a0002a0008others(1): Show | a0001c0001a0001c0019a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0027others(4): Show | a0001c0001t0001g0002a0001c0001t0001g0126a0001c0001t0001g0128others(7): Show | 10 | 142 | 0.0704 | 2 | c.516 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78199706 | C | CAT | intron_variant | MODIFIER | HG01884.hp1 HG03579.hp2 |
a0003a0012 | a0003c0004a0012c0016 | a0003c0004t0004a0012c0016t0014 | a0003c0004t0004g0013a0012c0016t0014g0136 | 2 | 142 | 0.0141 | 2 | c.516 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78202812 | G | GTT | intron_variant | MODIFIER | HG02015.hp1 HG02486.hp2 HG02683.hp1 others(4): Show |
a0001a0002a0005others(1): Show | a0001c0001a0002c0002a0005c0005others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(3): Show | a0001c0001t0001g0120a0001c0001t0003g0067a0001c0001t0003g0074others(4): Show | 7 | 142 | 0.0493 | 2 | c.516 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78213250 | C | CAA | intron_variant | MODIFIER | HG00741.hp2 HG01884.hp1 HG03139.hp1 others(2): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0004others(2): Show | a0001c0001t0001a0002c0002t0002a0003c0004t0004others(2): Show | a0001c0001t0001g0021a0002c0002t0002g0116a0003c0004t0004g0013others(2): Show | 5 | 142 | 0.0352 | 2 | c.516 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78229500 | C | CTA | intron_variant | MODIFIER | HG03098.hp1 NA18522.hp2 |
a0001a0013 | a0001c0001a0013c0015 | a0001c0001t0004a0013c0015t0001 | a0001c0001t0004g0084a0013c0015t0001g0094 | 2 | 142 | 0.0141 | 2 | c.516 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78229506 | C | CTG | intron_variant | MODIFIER | HG00735.hp1 HG00738.hp2 HG01071.hp2 others(11): Show |
a0001a0002a0016others(2): Show | a0001c0001a0002c0002a0016c0011others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0002a0001c0001t0001g0128a0001c0001t0002g0127others(11): Show | 14 | 142 | 0.0986 | 2 | c.516 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78229515 | G | GAT | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00735.hp2 others(50): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0007a0002c0002others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(50): Show | 53 | 142 | 0.3732 | 2 | c.516 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78233524 | A | ATT | intron_variant | MODIFIER | HG00738.hp2 HG01081.hp1 HG02145.hp1 others(7): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0004 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(5): Show | a0001c0001t0001g0022a0001c0001t0001g0137a0001c0001t0004g0053others(7): Show | 10 | 142 | 0.0704 | 2 | c.516 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78234802 | C | CAA | intron_variant | MODIFIER | HG02559.hp1 HG03139.hp2 HG03239.hp1 others(5): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0004others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(5): Show | a0001c0001t0001g0021a0001c0001t0003g0060a0001c0001t0006g0078others(5): Show | 8 | 142 | 0.0563 | 2 | c.516 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78237073 | C | CAA | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(25): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0019a0002c0002others(8): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(17): Show | a0001c0001t0001g0029a0001c0001t0001g0033a0001c0001t0001g0085others(25): Show | 28 | 142 | 0.1972 | 2 | c.516 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78254502 | G | GTT | intron_variant | MODIFIER | HG00438.hp1 HG00558.hp1 HG02109.hp2 others(16): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0019a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(9): Show | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0029others(16): Show | 19 | 142 | 0.1338 | 2 | c.516 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78261776 | C | CTA | intron_variant | MODIFIER | HG00558.hp1 HG02109.hp2 NA19030.hp2 others(1): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0006 | a0001c0001t0001a0002c0002t0005a0004c0006t0004 | a0001c0001t0001g0029a0001c0001t0001g0085a0002c0002t0005g0016others(1): Show | 4 | 142 | 0.0282 | 2 | c.516 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78261788 | C | CTA | intron_variant | MODIFIER | HG00735.hp2 HG00741.hp2 |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0115a0002c0002t0002g0116 | 2 | 142 | 0.0141 | 2 | c.516 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78261789 | T | TAG | intron_variant | MODIFIER | HG00438.hp2 HG00558.hp2 HG00735.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(3): Show | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0120others(6): Show | 9 | 142 | 0.0634 | 2 | c.516 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78261790 | A | ATC | intron_variant | MODIFIER | HG02559.hp1 HG02818.hp1 HG02965.hp2 others(4): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0007a0002c0022others(3): Show | a0001c0001t0006a0001c0001t0017a0001c0007t0007others(4): Show | a0001c0001t0006g0078a0001c0001t0017g0103a0001c0007t0007g0111others(4): Show | 7 | 142 | 0.0493 | 2 | c.516 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78263996 | C | CTT | intron_variant | MODIFIER | HG00438.hp1 HG01071.hp1 HG01109.hp2 others(8): Show |
a0001a0002a0013 | a0001c0001a0001c0007a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0126others(8): Show | 11 | 142 | 0.0775 | 2 | c.516 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78266788 | T | TTC | intron_variant | MODIFIER | HG01074.hp1 HG01952.hp1 HG03669.hp2 others(2): Show |
a0001a0005a0015 | a0001c0001a0005c0005a0015c0013 | a0001c0001t0001a0001c0001t0002a0005c0005t0003others(1): Show | a0001c0001t0001g0054a0001c0001t0002g0032a0001c0001t0002g0056others(2): Show | 5 | 142 | 0.0352 | 2 | c.516 others(23): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78293978 | G | GAA | intron_variant | MODIFIER | HG00741.hp1 HG01074.hp1 HG01346.hp1 others(9): Show |
a0001a0002a0006others(2): Show | a0001c0001a0002c0002a0006c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0020a0001c0001t0001g0033a0001c0001t0001g0054others(9): Show | 12 | 142 | 0.0845 | 2 | c.517 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78293983 | A | AAC | intron_variant | MODIFIER | HG00735.hp1 HG01192.hp2 HG01257.hp1 others(20): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0019a0002c0002others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0083a0001c0001t0001g0139a0001c0001t0002g0052others(20): Show | 23 | 142 | 0.1620 | 2 | c.517 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78312381 | C | CTT | intron_variant | MODIFIER | HG00609.hp1 HG02040.hp1 HG02257.hp2 others(13): Show |
a0001a0002a0005 | a0001c0001a0001c0019a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0083a0001c0001t0001g0139a0001c0001t0002g0052others(13): Show | 16 | 142 | 0.1127 | 2 | c.517 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78314688 | G | GGT | intron_variant | MODIFIER | HG02886.hp2 HG04115.hp2 NA19011.hp1 |
a0001a0003 | a0001c0001a0003c0017 | a0001c0001t0001a0001c0001t0012a0003c0017t0001 | a0001c0001t0001g0049a0001c0001t0012g0141a0003c0017t0001g0048 | 3 | 142 | 0.0211 | 2 | c.517 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78314688 | G | GTT | intron_variant | MODIFIER | HG00438.hp1 HG02683.hp2 HG03041.hp1 others(3): Show |
a0001a0003 | a0001c0001a0001c0007a0003c0004 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(2): Show | a0001c0001t0001g0126a0001c0001t0001g0142a0001c0001t0004g0121others(3): Show | 6 | 142 | 0.0423 | 2 | c.517 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78314707 | T | TTG | intron_variant | MODIFIER | HG00438.hp2 HG01071.hp1 HG01071.hp2 others(30): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0002c0022others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0020a0001c0001t0001g0054a0001c0001t0001g0093others(30): Show | 33 | 142 | 0.2324 | 2 | c.517 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78321277 | A | AAT | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0007a0002c0002others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(37): Show | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0022others(76): Show | 79 | 142 | 0.5563 | 2 | c.517 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78321382 | G | GTA | intron_variant | MODIFIER | HG02886.hp1 HG03041.hp1 HG03098.hp2 |
a0001a0006 | a0001c0007a0006c0003 | a0001c0007t0007a0006c0003t0015a0006c0003t0016 | a0001c0007t0007g0111a0006c0003t0015g0135a0006c0003t0016g0081 | 3 | 142 | 0.0211 | 2 | c.517 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78321394 | G | GTA | intron_variant | MODIFIER | HG01081.hp1 HG01109.hp2 HG02109.hp1 others(10): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0002c0022others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(9): Show | a0001c0001t0001g0093a0001c0001t0001g0137a0001c0001t0002g0015others(10): Show | 13 | 142 | 0.0916 | 2 | c.517 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78321420 | G | GTA | intron_variant | MODIFIER | HG02258.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
a0001a0005a0011 | a0001c0001a0005c0005a0011c0018 | a0001c0001t0001a0001c0001t0025a0005c0005t0002others(1): Show | a0001c0001t0001g0137a0001c0001t0025g0041a0005c0005t0002g0009others(1): Show | 4 | 142 | 0.0282 | 2 | c.517 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78326577 | G | GCC | intron_variant | MODIFIER | HG00735.hp2 HG00741.hp2 HG01952.hp1 others(10): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0004others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0021a0001c0001t0002g0056a0001c0001t0003g0065others(10): Show | 13 | 142 | 0.0916 | 2 | c.517 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
WWOX_chr16_78094654_79217667 | 78328213 | C | CAG | intron_variant | MODIFIER | HG01884.hp2 HG02809.hp1 HG03579.hp1 others(4): Show |
a0001a0003a0005others(1): Show | a0001c0001a0003c0004a0005c0005others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(4): Show | a0001c0001t0001g0022a0001c0001t0004g0084a0001c0001t0006g0078others(4): Show | 7 | 142 | 0.0493 | 2 | c.517 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar |