view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | 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 | 78912109 | T | TCTGA | intron_variant | MODIFIER | HG01257.hp1 HG01891.hp1 HG02258.hp1 others(9): Show |
a0001a0002a0003others(5): Show | a0001c0001a0002c0002a0003c0004others(5): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(8): Show | a0001c0001t0003g0106 a0001c0001t0004g0053 a0001c0001t0004g0112 others(9): Show |
12 | 142 | 0.0845 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78930222 | T | TCTTC | intron_variant | MODIFIER | HG00609.hp2 HG01071.hp1 HG01257.hp2 others(22): Show |
a0001a0002a0005others(2): Show | a0001c0001a0002c0002a0005c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(22): Show |
25 | 40 | 0.6250 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78937448 | C | CTTTT | intron_variant | MODIFIER | HG01074.hp1 HG01081.hp2 HG01192.hp2 others(5): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(3): Show | a0001c0001t0001g0054 a0001c0001t0003g0067 a0001c0001t0003g0074 others(5): Show |
8 | 44 | 0.1818 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78937601 | C | CTTCA | intron_variant | MODIFIER | HG00738.hp2 HG00741.hp1 HG01071.hp1 others(23): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0007a0002c0002others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0020 a0001c0001t0002g0015 a0001c0001t0002g0032 others(23): Show |
26 | 116 | 0.2241 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78937601 | C | CTTTA | intron_variant | MODIFIER | HG01891.hp1 NA18957.hp1 NA19030.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0017a0001c0001t0027 | a0001c0001t0001g0128 a0001c0001t0017g0103 a0001c0001t0027g0096 |
3 | 93 | 0.0323 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78950533 | T | TACAC | intron_variant | MODIFIER | HG00738.hp2 HG00741.hp1 HG01074.hp1 others(17): Show |
a0001a0002a0009others(4): Show | a0001c0001a0002c0002a0009c0010others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0022 a0001c0001t0001g0054 a0001c0001t0001g0085 others(17): Show |
20 | 41 | 0.4878 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78957007 | C | CTCCG | intron_variant | MODIFIER | HG02258.hp2 HG02922.hp1 HG02922.hp2 |
a0001a0002a0014 | a0001c0001a0002c0002a0014c0018 | a0001c0001t0013a0002c0002t0001a0014c0018t0002 | a0001c0001t0013g0102 a0002c0002t0001g0010 a0014c0018t0002g0131 |
3 | 142 | 0.0211 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78971436 | C | CAGAG | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(85): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0007a0002c0002others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(44): Show | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0024 others(85): Show |
88 | 142 | 0.6197 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78977976 | C | CATCT | intron_variant | MODIFIER | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(99): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0007a0002c0002others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(46): Show | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0020 others(99): Show |
102 | 142 | 0.7183 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78983870 | C | CTTTT | intron_variant | MODIFIER | HG00735.hp1 HG00738.hp1 HG01071.hp1 others(14): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0002c0022others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0021 a0001c0001t0002g0015 a0001c0001t0002g0056 others(14): Show |
17 | 44 | 0.3864 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78989821 | C | CGTGT | intron_variant | MODIFIER | HG01081.hp1 HG02572.hp1 HG03579.hp1 others(2): Show |
a0001a0003a0004others(2): Show | a0001c0001a0003c0004a0004c0006others(2): Show | a0001c0001t0001a0003c0004t0004a0004c0006t0001others(2): Show | a0001c0001t0001g0033 a0003c0004t0004g0055 a0004c0006t0001g0132 others(2): Show |
5 | 49 | 0.1020 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 78989824 | G | GTGTT | intron_variant | MODIFIER | HG01071.hp2 HG02965.hp2 NA20752.hp2 |
a0001a0002 | a0001c0001a0002c0002a0002c0022 | a0001c0001t0003a0002c0002t0006a0002c0022t0007 | a0001c0001t0003g0062 a0002c0002t0006g0063 a0002c0022t0007g0109 |
3 | 142 | 0.0211 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 79011459 | T | TTTTA | intron_variant | MODIFIER | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(49): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0019a0002c0002others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(29): Show | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0021 others(49): Show |
52 | 104 | 0.5000 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 79017429 | C | CAAAA | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp1 HG02965.hp2 others(4): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0022a0003c0004others(2): Show | a0001c0001t0001a0001c0001t0027a0002c0022t0007others(4): Show | a0001c0001t0001g0119 a0001c0001t0027g0096 a0002c0022t0007g0109 others(4): Show |
7 | 26 | 0.2692 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 79019181 | A | AAAAG | intron_variant | MODIFIER | HG01074.hp2 HG01496.hp1 HG02258.hp2 others(2): Show |
a0002a0005a0006others(1): Show | a0002c0002a0005c0003a0006c0005others(1): Show | a0002c0002t0002a0002c0002t0012a0005c0003t0019others(2): Show | a0002c0002t0002g0099 a0002c0002t0012g0098 a0005c0003t0019g0011 others(2): Show |
5 | 135 | 0.0370 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 79019188 | A | AAAAG | intron_variant | MODIFIER | HG00438.hp1 HG00558.hp2 HG00741.hp2 others(31): Show |
a0001a0002a0004others(6): Show | a0001c0001a0001c0019a0002c0002others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0023 others(31): Show |
34 | 124 | 0.2742 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 79023956 | A | AAAAC | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(112): Show |
a0001a0002a0003others(16): Show | a0001c0001a0001c0007a0001c0019others(22): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(56): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(112): Show |
115 | 142 | 0.8099 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 79031893 | C | CATAT | intron_variant | MODIFIER | HG02145.hp1 HG02258.hp2 HG02559.hp1 others(1): Show |
a0001a0003a0004others(1): Show | a0001c0001a0003c0004a0004c0023others(1): Show | a0001c0001t0022a0003c0004t0001a0004c0023t0001others(1): Show | a0001c0001t0022g0088 a0003c0004t0001g0097 a0004c0023t0001g0001 others(1): Show |
4 | 101 | 0.0396 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 79038832 | G | GAGCC | intron_variant | MODIFIER | HG01884.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
a0002a0003a0005others(1): Show | a0002c0002a0003c0004a0005c0003others(1): Show | a0002c0002t0001a0003c0004t0004a0005c0003t0016others(1): Show | a0002c0002t0001g0010 a0003c0004t0004g0091 a0005c0003t0016g0081 others(1): Show |
4 | 142 | 0.0282 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 79042728 | G | GTTTT | intron_variant | MODIFIER | HG02486.hp2 HG02572.hp1 HG02572.hp2 others(2): Show |
a0001a0003a0006others(1): Show | a0001c0001a0003c0017a0006c0005others(1): Show | a0001c0001t0001a0003c0017t0001a0006c0005t0001others(2): Show | a0001c0001t0001g0093 a0003c0017t0001g0048 a0006c0005t0001g0059 others(2): Show |
5 | 18 | 0.2778 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 79070268 | A | ATGTG | intron_variant | MODIFIER | NA19030.hp2 NA20129.hp1 |
a0001a0004 | a0001c0001a0004c0006 | a0001c0001t0005a0004c0006t0004 | a0001c0001t0005g0050 a0004c0006t0004g0082 |
2 | 43 | 0.0465 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 79090280 | C | CGTGT | intron_variant | MODIFIER | HG00741.hp2 HG01081.hp1 HG01109.hp1 others(16): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0004others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0093 others(16): Show |
19 | 54 | 0.3519 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 79096016 | A | ATTTT | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(33): Show |
a0001a0002a0003others(6): Show | a0001c0001a0002c0002a0003c0004others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0033 others(33): Show |
36 | 79 | 0.4557 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 79099593 | T | TGAGA | intron_variant | MODIFIER | HG01346.hp1 HG03942.hp2 |
a0001a0010 | a0001c0001a0010c0021 | a0001c0001t0003a0010c0021t0002 | a0001c0001t0003g0060 a0010c0021t0002g0089 |
2 | 92 | 0.0217 | 4 | c.105 others(27): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 79132127 | A | AACAC | intron_variant | MODIFIER | HG01257.hp2 HG01258.hp1 HG02559.hp1 |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0003c0004t0001 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0003c0004t0001g0097 |
3 | 47 | 0.0638 | 4 | 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 | 79163816 | A | AAAAG | intron_variant | MODIFIER | HG01081.hp1 HG02145.hp1 HG02145.hp2 others(8): Show |
a0001a0003a0004others(2): Show | a0001c0001a0001c0007a0003c0004others(4): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(8): Show | a0001c0001t0001g0003 a0001c0001t0004g0004 a0001c0001t0008g0086 others(8): Show |
11 | 28 | 0.3929 | 4 | 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 | 79163884 | G | GAAAA | intron_variant | MODIFIER | HG00609.hp2 HG01346.hp2 HG01884.hp1 others(15): Show |
a0001a0002a0006others(4): Show | a0001c0001a0001c0019a0002c0002others(5): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(10): Show | a0001c0001t0001g0012 a0001c0001t0001g0042 a0001c0001t0001g0085 others(15): Show |
18 | 46 | 0.3913 | 4 | 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 | 79170616 | T | TAAAA | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(116): Show |
a0001a0002a0003others(16): Show | a0001c0001a0001c0007a0001c0019others(21): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(56): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(116): Show |
119 | 142 | 0.8380 | 4 | 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 | 79177376 | T | TCTCC | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(99): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0007a0001c0019others(19): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(46): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0021 others(99): Show |
102 | 142 | 0.7183 | 4 | 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 | 79210710 | T | TTTAA | intron_variant | MODIFIER | HG02109.hp1 HG02258.hp2 HG02965.hp2 others(3): Show |
a0001a0002a0008others(1): Show | a0001c0001a0001c0007a0002c0002others(3): Show | a0001c0001t0017a0001c0007t0007a0002c0002t0007others(3): Show | a0001c0001t0017g0103 a0001c0007t0007g0110 a0002c0002t0007g0047 others(3): Show |
6 | 142 | 0.0423 | 4 | c.105 others(21): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWOX_chr16_78094654_79217667 | 79212906 | T | TAAAG | downstream_gene_variant | MODIFIER | HG00735.hp2 HG00738.hp2 HG00741.hp2 others(62): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0007a0001c0019others(14): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(39): Show | a0001c0001t0002g0015 a0001c0001t0002g0032 a0001c0001t0002g0044 others(62): Show |
65 | 142 | 0.4577 | 4 | c.*11 others(15): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 240 | chr16 | TogoVar | |||||||
WWOX_chr16_78094654_79217667 | 79212963 | A | ATTAC | downstream_gene_variant | MODIFIER | HG01081.hp1 HG02886.hp1 HG03486.hp2 |
a0001a0003a0005 | a0001c0007a0003c0004a0005c0003 | a0001c0007t0009a0003c0004t0004a0005c0003t0016 | a0001c0007t0009g0111 a0003c0004t0004g0055 a0005c0003t0016g0081 |
3 | 142 | 0.0211 | 4 | c.*11 others(15): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 297 | chr16 | TogoVar | |||||||
WWOX_chr16_78094654_79217667 | 79213030 | G | GTGAT | downstream_gene_variant | MODIFIER | HG00735.hp2 HG00738.hp2 HG00741.hp2 others(69): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0007a0002c0002others(14): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(42): Show | a0001c0001t0002g0015 a0001c0001t0002g0032 a0001c0001t0002g0044 others(69): Show |
72 | 142 | 0.5070 | 4 | c.*12 others(15): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 364 | chr16 | TogoVar | |||||||
WWOX_chr16_78094654_79217667 | 79213687 | C | CAGTT | downstream_gene_variant | MODIFIER | HG02486.hp1 HG02559.hp1 HG02559.hp2 others(4): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0004others(2): Show | a0001c0001t0001a0002c0002t0003a0003c0004t0001others(2): Show | a0001c0001t0001g0003 a0001c0001t0001g0012 a0002c0002t0003g0077 others(4): Show |
7 | 142 | 0.0493 | 4 | c.*18 others(15): Show |
WWOX | ENSG00000186153.19 | transcript | ENST00000566780.6 | protein_coding | 1021 | chr16 | TogoVar | |||||||
WWP1_chr8_86337547_86473503 | 86352220 | T | TTTTA | intron_variant | MODIFIER | HG01069.hp1 HG01256.hp1 HG02145.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0013 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(3): Show |
7 | 207 | 0.0338 | 4 | c.-11 others(23): Show |
WWP1 | ENSG00000123124.14 | transcript | ENST00000517970.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
WWP1_chr8_86337547_86473503 | 86362163 | C | CATAT | intron_variant | MODIFIER | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(30): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0255 a0001c0001t0002g0015 a0001c0001t0002g0038 others(30): Show |
33 | 66 | 0.5000 | 4 | c.-11 others(23): Show |
WWP1 | ENSG00000123124.14 | transcript | ENST00000517970.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
WWP1_chr8_86337547_86473503 | 86364806 | C | CGAAA | intron_variant | MODIFIER | HG00639.hp1 HG00741.hp2 HG01069.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(3): Show |
6 | 279 | 0.0215 | 4 | c.-11 others(23): Show |
WWP1 | ENSG00000123124.14 | transcript | ENST00000517970.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
WWP1_chr8_86337547_86473503 | 86364833 | A | AAGAG | intron_variant | MODIFIER | HG00642.hp2 HG01243.hp1 HG01261.hp2 others(26): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0002t0006others(1): Show | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(26): Show |
29 | 171 | 0.1696 | 4 | c.-11 others(23): Show |
WWP1 | ENSG00000123124.14 | transcript | ENST00000517970.6 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
WWP1_chr8_86337547_86473503 | 86370855 | C | CTTTT | intron_variant | MODIFIER | HG01069.hp1 HG01256.hp1 HG01261.hp2 others(8): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0002t0013a0001c0003t0001 | a0001c0002t0001g0172 a0001c0002t0001g0270 a0001c0002t0001g0271 others(8): Show |
11 | 99 | 0.1111 | 4 | c.-22 others(21): Show |
WWP1 | ENSG00000123124.14 | transcript | ENST00000517970.6 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
WWP1_chr8_86337547_86473503 | 86394933 | T | TAAAA | intron_variant | MODIFIER | HG00639.hp2 HG00741.hp1 HG01175.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0015 | a0001c0001t0001g0160 a0001c0001t0001g0202 a0001c0001t0001g0203 others(7): Show |
10 | 103 | 0.0971 | 4 | c.335 others(21): Show |
WWP1 | ENSG00000123124.14 | transcript | ENST00000517970.6 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
WWP1_chr8_86337547_86473503 | 86414227 | C | CTGTG | intron_variant | MODIFIER | HG00738.hp2 HG00741.hp1 HG01081.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0181 a0001c0001t0001g0203 a0001c0001t0001g0224 others(3): Show |
6 | 118 | 0.0508 | 4 | c.106 others(23): Show |
WWP1 | ENSG00000123124.14 | transcript | ENST00000517970.6 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
WWP1_chr8_86337547_86473503 | 86422319 | G | GTATT | intron_variant | MODIFIER | HG00735.hp1 HG01070.hp2 HG01109.hp1 others(18): Show |
a0001a0004 | a0001c0001a0004c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(17): Show |
21 | 161 | 0.1304 | 4 | c.106 others(23): Show |
WWP1 | ENSG00000123124.14 | transcript | ENST00000517970.6 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
WWP1_chr8_86337547_86473503 | 86451050 | A | AAAAT | intron_variant | MODIFIER | HG02145.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 |
4 | 298 | 0.0134 | 4 | c.227 others(23): Show |
WWP1 | ENSG00000123124.14 | transcript | ENST00000517970.6 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
WWP1_chr8_86337547_86473503 | 86451214 | T | TAAAA | intron_variant | MODIFIER | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(23): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0166 a0001c0001t0001g0175 a0001c0001t0001g0176 others(23): Show |
26 | 32 | 0.8125 | 4 | c.227 others(23): Show |
WWP1 | ENSG00000123124.14 | transcript | ENST00000517970.6 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
WWP1_chr8_86337547_86473503 | 86471343 | G | GACCT | downstream_gene_variant | MODIFIER | HG00639.hp1 HG00741.hp2 HG01069.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0262 a0001c0001t0005g0263 a0001c0001t0005g0264 others(3): Show |
6 | 298 | 0.0201 | 4 | c.*44 others(15): Show |
WWP1 | ENSG00000123124.14 | transcript | ENST00000517970.6 | protein_coding | 2841 | chr8 | TogoVar | |||||||
WWP2_chr16_69757332_69946739 | 69761120 | C | CAAAT | upstream_gene_variant | MODIFIER | HG00735.hp1 HG01074.hp2 HG01169.hp1 others(28): Show |
a0001a0008 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0005others(6): Show | a0001c0001t0001g0043 a0001c0001t0001g0159 a0001c0001t0001g0162 others(28): Show |
31 | 310 | 0.1000 | 4 | c.-12 others(15): Show |
WWP2 | ENSG00000198373.13 | transcript | ENST00000359154.7 | protein_coding | 1211 | chr16 | TogoVar | |||||||
WWP2_chr16_69757332_69946739 | 69778072 | A | AATAT | intron_variant | MODIFIER | HG02132.hp2 HG02895.hp2 HG03098.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0012 | a0001c0001t0001a0001c0002t0013a0001c0012t0009 | a0001c0001t0001g0049 a0001c0002t0013g0298 a0001c0012t0009g0289 others(1): Show |
4 | 127 | 0.0315 | 4 | c.-15 others(21): Show |
WWP2 | ENSG00000198373.13 | transcript | ENST00000359154.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWP2_chr16_69757332_69946739 | 69778173 | A | AATAT | intron_variant | MODIFIER | NA18971.hp1 NA18975.hp2 NA19000.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0001g0057 |
3 | 281 | 0.0107 | 4 | c.-15 others(21): Show |
WWP2 | ENSG00000198373.13 | transcript | ENST00000359154.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWP2_chr16_69757332_69946739 | 69778192 | A | ATATT | intron_variant | MODIFIER | HG00609.hp1 HG02074.hp2 HG02738.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0003 | a0001c0001t0001g0040 a0001c0001t0001g0058 a0001c0001t0001g0070 others(6): Show |
9 | 117 | 0.0769 | 4 | c.-15 others(21): Show |
WWP2 | ENSG00000198373.13 | transcript | ENST00000359154.7 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
WWP2_chr16_69757332_69946739 | 69791224 | T | TTTTC | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(15): Show |
a0001 | a0001c0006a0001c0009a0001c0014 | a0001c0006t0001a0001c0009t0001a0001c0009t0004others(1): Show | a0001c0006t0001g0258 a0001c0006t0001g0259 a0001c0006t0001g0260 others(15): Show |
18 | 312 | 0.0577 | 4 | c.70+ others(19): Show |
WWP2 | ENSG00000198373.13 | transcript | ENST00000359154.7 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr16 | TogoVar |