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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
THSD7B_chr2_136760545_137682718 | 137238534 | C | CTTT | intron_variant | MODIFIER | HG00609.hp2 HG01167.hp1 HG01515.hp1 others(13): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0004a0001c0005others(10): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(13): Show | a0001c0001t0001g0062 a0001c0001t0003g0081 a0001c0001t0010g0087 others(13): Show |
16 | 98 | 0.1633 | 3 | c.215 others(22): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 9/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137252266 | C | CAAA | intron_variant | MODIFIER | HG00735.hp2 HG02280.hp2 HG03225.hp2 others(1): Show |
a0001a0002a0004 | a0001c0021a0002c0030a0002c0044others(1): Show | a0001c0021t0004a0002c0030t0004a0002c0044t0007others(1): Show | a0001c0021t0004g0071 a0002c0030t0004g0050 a0002c0044t0007g0059 others(1): Show |
4 | 98 | 0.0408 | 3 | c.226 others(22): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 10/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137348703 | C | CTTT | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(3): Show |
a0003a0004a0021 | a0003c0002a0003c0040a0004c0007others(1): Show | a0003c0002t0002a0003c0002t0015a0003c0040t0011others(2): Show | a0003c0002t0002g0061 a0003c0002t0015g0038 a0003c0040t0011g0080 others(3): Show |
6 | 98 | 0.0612 | 3 | c.250 others(24): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137372323 | C | CTTT | intron_variant | MODIFIER | HG01167.hp2 HG01255.hp2 HG02630.hp1 others(1): Show |
a0003a0004 | a0003c0002a0003c0014a0004c0007 | a0003c0002t0002a0003c0002t0015a0003c0014t0018others(1): Show | a0003c0002t0002g0061 a0003c0002t0015g0038 a0003c0014t0018g0094 others(1): Show |
4 | 98 | 0.0408 | 3 | c.250 others(24): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137389402 | A | ATTT | intron_variant | MODIFIER | HG01358.hp1 HG02056.hp1 NA18990.hp2 others(1): Show |
a0002a0010a0012 | a0002c0016a0002c0020a0010c0035others(1): Show | a0002c0016t0001a0002c0020t0004a0010c0035t0001others(1): Show | a0002c0016t0001g0028 a0002c0020t0004g0068 a0010c0035t0001g0063 others(1): Show |
4 | 98 | 0.0408 | 3 | c.250 others(24): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137405198 | C | CAAA | intron_variant | MODIFIER | HG00438.hp2 HG01169.hp1 HG02258.hp2 others(10): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0004a0001c0005others(8): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0001others(10): Show | a0001c0001t0001g0026 a0001c0001t0003g0081 a0001c0004t0001g0058 others(10): Show |
13 | 98 | 0.1327 | 3 | c.250 others(20): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 12/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137412893 | C | CTTT | intron_variant | MODIFIER | HG00735.hp2 HG02257.hp2 HG02258.hp1 others(15): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0010a0002c0003others(12): Show | a0001c0001t0001a0001c0001t0008a0001c0010t0002others(14): Show | a0001c0001t0001g0062 a0001c0001t0008g0012 a0001c0010t0002g0020 others(15): Show |
18 | 98 | 0.1837 | 3 | c.295 others(22): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137419415 | C | CTCG | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(34): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0004a0001c0005others(22): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0029 others(34): Show |
37 | 98 | 0.3776 | 3 | c.295 others(22): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 14/27 | chr2 | TogoVar | |||||||
THSD7B_chr2_136760545_137682718 | 137419429 | G | GCGC | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(34): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0004a0001c0005others(22): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0029 others(34): Show |
37 | 98 | 0.3776 | 3 | c.295 others(22): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 14/27 | chr2 | TogoVar | |||||||
THSD7B_chr2_136760545_137682718 | 137421049 | C | CCTT | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(93): Show |
a0001a0002a0003others(19): Show | a0001c0001a0001c0004a0001c0005others(54): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(79): Show | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0027 others(93): Show |
96 | 98 | 0.9796 | 3 | c.295 others(22): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137425099 | G | GATA | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00609.hp1 others(73): Show |
a0001a0002a0003others(17): Show | a0001c0001a0001c0004a0001c0005others(44): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(66): Show | a0001c0001t0001g0018 a0001c0001t0001g0026 a0001c0001t0001g0027 others(73): Show |
76 | 98 | 0.7755 | 3 | c.295 others(24): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137446667 | A | AAAG | intron_variant | MODIFIER | HG02280.hp1 HG03453.hp1 |
a0001 | a0001c0001a0001c0019 | a0001c0001t0002a0001c0019t0016 | a0001c0001t0002g0034 a0001c0019t0016g0090 |
2 | 98 | 0.0204 | 3 | c.296 others(22): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137448800 | A | AAAC | intron_variant | MODIFIER | HG01167.hp1 HG01255.hp1 HG01515.hp1 others(7): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0004a0001c0036others(6): Show | a0001c0001t0002a0001c0001t0010a0001c0004t0003others(7): Show | a0001c0001t0002g0034 a0001c0001t0010g0087 a0001c0004t0003g0091 others(7): Show |
10 | 98 | 0.1020 | 3 | c.296 others(22): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 14/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137453326 | C | CTTT | intron_variant | MODIFIER | HG02280.hp2 HG02647.hp2 HG02897.hp1 others(1): Show |
a0001a0002a0006others(1): Show | a0001c0004a0002c0044a0006c0011others(1): Show | a0001c0004t0003a0002c0044t0007a0006c0011t0003others(1): Show | a0001c0004t0003g0091 a0002c0044t0007g0059 a0006c0011t0003g0092 others(1): Show |
4 | 98 | 0.0408 | 3 | c.313 others(22): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137487374 | C | CAAA | intron_variant | MODIFIER | HG01255.hp1 HG01358.hp2 HG02622.hp1 others(8): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0004a0002c0003others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0003others(8): Show | a0001c0001t0001g0018 a0001c0001t0003g0081 a0001c0004t0003g0091 others(8): Show |
11 | 98 | 0.1122 | 3 | c.313 others(24): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137493122 | C | CAAA | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 HG01255.hp2 others(8): Show |
a0001a0003a0004others(2): Show | a0001c0001a0003c0002a0003c0040others(4): Show | a0001c0001t0001a0001c0001t0002a0003c0002t0002others(7): Show | a0001c0001t0001g0027 a0001c0001t0002g0025 a0003c0002t0002g0061 others(8): Show |
11 | 98 | 0.1122 | 3 | c.313 others(24): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137523171 | A | AGTT | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(68): Show |
a0001a0002a0003others(13): Show | a0001c0001a0001c0004a0001c0005others(40): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(58): Show | a0001c0001t0001g0027 a0001c0001t0001g0052 a0001c0001t0001g0062 others(68): Show |
71 | 98 | 0.7245 | 3 | c.313 others(24): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137546468 | A | ATAT | intron_variant | MODIFIER | HG02258.hp1 HG02630.hp2 HG02886.hp1 others(9): Show |
a0001a0002a0005others(3): Show | a0001c0001a0001c0004a0001c0010others(7): Show | a0001c0001t0001a0001c0004t0003a0001c0010t0002others(8): Show | a0001c0001t0001g0062 a0001c0004t0003g0091 a0001c0010t0002g0020 others(9): Show |
12 | 98 | 0.1225 | 3 | c.313 others(24): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 15/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137569793 | A | AATT | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG00738.hp2 others(26): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0005a0001c0017others(20): Show | a0001c0001t0002a0001c0001t0010a0001c0005t0001others(26): Show | a0001c0001t0002g0034 a0001c0001t0010g0087 a0001c0005t0001g0022 others(26): Show |
29 | 98 | 0.2959 | 3 | c.327 others(22): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 16/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137596244 | A | AGAT | intron_variant | MODIFIER | HG00438.hp2 HG00735.hp2 HG01169.hp1 others(32): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0004a0001c0005others(22): Show | a0001c0001t0002a0001c0001t0008a0001c0004t0001others(28): Show | a0001c0001t0002g0025 a0001c0001t0002g0034 a0001c0001t0008g0012 others(32): Show |
35 | 98 | 0.3571 | 3 | c.342 others(24): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 17/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137646650 | T | TTAA | intron_variant | MODIFIER | HG00438.hp2 HG00738.hp2 HG02257.hp1 others(5): Show |
a0001a0003a0008 | a0001c0053a0001c0056a0003c0002others(2): Show | a0001c0053t0005a0001c0056t0003a0003c0002t0001others(4): Show | a0001c0053t0005g0084 a0001c0056t0003g0086 a0003c0002t0001g0002 others(5): Show |
8 | 98 | 0.0816 | 3 | c.394 others(22): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD7B_chr2_136760545_137682718 | 137668446 | C | CAAA | intron_variant | MODIFIER | HG00438.hp2 HG02257.hp2 HG02622.hp2 others(5): Show |
a0001a0006a0008others(2): Show | a0001c0013a0001c0021a0006c0023others(4): Show | a0001c0013t0002a0001c0021t0004a0006c0023t0002others(4): Show | a0001c0013t0002g0030 a0001c0013t0002g0072 a0001c0021t0004g0071 others(5): Show |
8 | 98 | 0.0816 | 3 | c.473 others(20): Show |
THSD7B | ENSG00000144229.13 | transcript | ENST00000409968.6 | protein_coding | 27/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
THSD8_chr19_12797069_12809389 | 12803911 | C | CAAA | intron_variant | MODIFIER | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(27): Show |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0001a0003c0003t0001 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0003c0003t0001g0004 |
30 | 420 | 0.0714 | 3 | c.149 others(18): Show |
THSD8 | ENSG00000284491.3 | transcript | ENST00000639810.3 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
THSD8_chr19_12797069_12809389 | 12805131 | C | CAAA | downstream_gene_variant | MODIFIER | HG02280.hp1 HG02486.hp1 HG02622.hp2 others(4): Show |
a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0004 a0003c0003t0001g0006 |
7 | 420 | 0.0167 | 3 | c.*82 others(12): Show |
THSD8 | ENSG00000284491.3 | transcript | ENST00000639810.3 | protein_coding | 743 | chr19 | TogoVar | |||||||
THTPA_chr14_23551271_23565271 | 23557760 | T | TTTC | intron_variant | MODIFIER | HG01106.hp2 HG01243.hp2 HG02109.hp2 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0008a0001c0001t0009 | a0001c0001t0003g0003 a0001c0001t0008g0003 a0001c0001t0009g0003 |
18 | 404 | 0.0446 | 3 | c.547 others(18): Show |
THTPA | ENSG00000259431.6 | transcript | ENST00000288014.7 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
THUMPD1_chr16_20728664_20746818 | 20742641 | C | CAAA | upstream_gene_variant | MODIFIER | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(22): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0008a0001c0001t0010a0001c0001t0013others(4): Show | a0001c0001t0008g0009 a0001c0001t0008g0055 a0001c0001t0008g0056 others(8): Show |
25 | 410 | 0.0610 | 3 | c.-90 others(12): Show |
THUMPD1 | ENSG00000066654.14 | transcript | ENST00000396083.7 | protein_coding | 824 | chr16 | TogoVar | |||||||
THUMPD2_chr2_39731061_39784258 | 39751681 | A | ATTT | intron_variant | MODIFIER | HG00621.hp1 HG00621.hp2 HG01175.hp1 others(19): Show |
a0001a0008a0009 | a0001c0001a0001c0002a0008c0013others(1): Show | a0001c0001t0001a0001c0002t0001a0008c0013t0001others(1): Show | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0071 others(13): Show |
22 | 338 | 0.0651 | 3 | c.107 others(22): Show |
THUMPD2 | ENSG00000138050.15 | transcript | ENST00000505747.6 | protein_coding | 8/9 | chr2 | TogoVar | |||||||
THUMPD2_chr2_39731061_39784258 | 39756909 | G | GTAA | intron_variant | MODIFIER | HG00741.hp2 HG01109.hp1 HG02109.hp2 others(12): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(2): Show | a0001c0001t0001g0017 a0001c0001t0001g0036 a0001c0001t0001g0062 others(11): Show |
15 | 338 | 0.0444 | 3 | c.892 others(18): Show |
THUMPD2 | ENSG00000138050.15 | transcript | ENST00000505747.6 | protein_coding | 6/9 | chr2 | TogoVar | |||||||
THUMPD3_chr3_9358054_9391791 | 9369309 | C | CAAA | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp2 HG02080.hp2 others(10): Show |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0005a0001c0002t0008others(2): Show | a0001c0002t0002g0016 a0001c0002t0002g0044 a0001c0002t0002g0168 others(6): Show |
13 | 378 | 0.0344 | 3 | c.331 others(20): Show |
THUMPD3 | ENSG00000134077.16 | transcript | ENST00000452837.7 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
TIA1_chr2_70204444_70253628 | 70208977 | G | GTTT | downstream_gene_variant | MODIFIER | HG00673.hp1 HG01074.hp1 HG01943.hp2 others(28): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0011a0001c0001t0025 | a0001c0001t0002g0019 a0001c0001t0002g0285 a0001c0001t0002g0289 others(27): Show |
31 | 394 | 0.0787 | 3 | c.*37 others(14): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 466 | chr2 | TogoVar | |||||||
TIA1_chr2_70204444_70253628 | 70230652 | C | CAAA | intron_variant | MODIFIER | HG00621.hp2 HG02155.hp1 NA18953.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0009 a0001c0001t0001g0112 a0001c0001t0001g0118 others(8): Show |
12 | 394 | 0.0305 | 3 | c.222 others(18): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 3/12 | chr2 | TogoVar | |||||||
TIA1_chr2_70204444_70253628 | 70232540 | C | CAAA | intron_variant | MODIFIER | HG02083.hp2 NA18943.hp1 NA18962.hp2 others(6): Show |
a0001 | a0001c0001a0001c0009 | a0001c0001t0001a0001c0009t0001 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0195 others(6): Show |
9 | 394 | 0.0228 | 3 | c.124 others(20): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 2/12 | chr2 | TogoVar | |||||||
TIA1_chr2_70204444_70253628 | 70242494 | C | CAAA | intron_variant | MODIFIER | HG00621.hp1 HG00642.hp1 HG00735.hp2 others(24): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(2): Show | a0001c0001t0002g0323 a0001c0001t0002g0324 a0001c0001t0003g0004 others(21): Show |
27 | 394 | 0.0685 | 3 | c.26+ others(18): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | TogoVar | |||||||
TIA1_chr2_70204444_70253628 | 70245914 | A | ATTT | intron_variant | MODIFIER | HG00735.hp2 HG01175.hp1 HG01257.hp2 others(26): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(1): Show | a0001c0001t0001g0069 a0001c0001t0003g0004 a0001c0001t0003g0027 others(25): Show |
29 | 394 | 0.0736 | 3 | c.26+ others(18): Show |
TIA1 | ENSG00000116001.17 | transcript | ENST00000433529.7 | protein_coding | 1/12 | chr2 | TogoVar | |||||||
TIAL1_chr10_119568465_119601964 | 119574586 | C | CAAA | 3_prime_UTR_variant | MODIFIER | HG00621.hp2 HG01346.hp2 HG01884.hp1 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0011a0001c0001t0024others(2): Show | a0001c0001t0006g0039 a0001c0001t0006g0042 a0001c0001t0006g0160 others(11): Show |
17 | 398 | 0.0427 | 3 | c.*10 others(14): Show |
TIAL1 | ENSG00000151923.18 | transcript | ENST00000436547.7 | protein_coding | 12/12 | 1078 | chr10 | TogoVar | ||||||
TIAL1_chr10_119568465_119601964 | 119585985 | T | TCCA | intron_variant | MODIFIER | HG02818.hp2 HG02922.hp1 HG02970.hp2 others(1): Show |
a0001 | a0001c0003 | a0001c0003t0008 | a0001c0003t0008g0023 a0001c0003t0008g0245 |
4 | 398 | 0.0101 | 3 | c.129 others(20): Show |
TIAL1 | ENSG00000151923.18 | transcript | ENST00000436547.7 | protein_coding | 2/11 | chr10 | TogoVar | |||||||
TIAL1_chr10_119568465_119601964 | 119595437 | T | TAAA | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(103): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(9): Show | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0013 others(79): Show |
106 | 398 | 0.2663 | 3 | c.32+ others(16): Show |
TIAL1 | ENSG00000151923.18 | transcript | ENST00000436547.7 | protein_coding | 1/11 | chr10 | TogoVar | |||||||
TIAM1_chr21_31113418_31349261 | 31153897 | C | CAAA | intron_variant | MODIFIER | HG00735.hp1 HG00741.hp1 HG01109.hp1 others(20): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0009others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(12): Show | a0001c0001t0002g0142 a0001c0001t0003g0024 a0001c0001t0003g0027 others(20): Show |
23 | 212 | 0.1085 | 3 | c.317 others(20): Show |
TIAM1 | ENSG00000156299.15 | transcript | ENST00000541036.6 | protein_coding | 17/27 | chr21 | TogoVar | |||||||
TIAM1_chr21_31113418_31349261 | 31169294 | A | AAAT | intron_variant | MODIFIER | HG00639.hp1 HG00639.hp2 HG01106.hp2 others(16): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0006others(2): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(8): Show | a0001c0001t0002g0108 a0001c0001t0002g0118 a0001c0001t0002g0150 others(16): Show |
19 | 212 | 0.0896 | 3 | c.288 others(22): Show |
TIAM1 | ENSG00000156299.15 | transcript | ENST00000541036.6 | protein_coding | 15/27 | chr21 | TogoVar | |||||||
TIAM1_chr21_31113418_31349261 | 31171035 | C | CAAA | intron_variant | MODIFIER | HG01952.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0026others(4): Show | a0001c0001t0002a0001c0001t0009a0001c0002t0004others(7): Show | a0001c0001t0002g0162 a0001c0001t0009g0202 a0001c0002t0004g0145 others(9): Show |
12 | 212 | 0.0566 | 3 | c.288 others(22): Show |
TIAM1 | ENSG00000156299.15 | transcript | ENST00000541036.6 | protein_coding | 15/27 | chr21 | TogoVar | |||||||
TIAM1_chr21_31113418_31349261 | 31189044 | C | CTTT | intron_variant | MODIFIER | HG01106.hp1 HG02486.hp1 HG02486.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0006 | a0001c0001t0002a0001c0001t0003a0001c0001t0031others(4): Show | a0001c0001t0002g0073 a0001c0001t0003g0013 a0001c0001t0003g0048 others(6): Show |
9 | 212 | 0.0425 | 3 | c.257 others(22): Show |
TIAM1 | ENSG00000156299.15 | transcript | ENST00000541036.6 | protein_coding | 13/27 | chr21 | TogoVar | |||||||
TIAM1_chr21_31113418_31349261 | 31203114 | T | TTTG | intron_variant | MODIFIER | HG03195.hp2 HG03540.hp1 NA21309.hp1 |
a0001a0011 | a0001c0001a0001c0021a0011c0019 | a0001c0001t0002a0001c0021t0022a0011c0019t0001 | a0001c0001t0002g0077 a0001c0021t0022g0107 a0011c0019t0001g0087 |
3 | 212 | 0.0142 | 3 | c.238 others(20): Show |
TIAM1 | ENSG00000156299.15 | transcript | ENST00000541036.6 | protein_coding | 11/27 | chr21 | TogoVar | |||||||
TIAM1_chr21_31113418_31349261 | 31210631 | A | AGGG | intron_variant | MODIFIER | HG01257.hp1 HG01891.hp1 NA18948.hp2 others(3): Show |
a0001a0007 | a0001c0001a0001c0018a0001c0025others(1): Show | a0001c0001t0002a0001c0001t0010a0001c0001t0027others(3): Show | a0001c0001t0002g0188 a0001c0001t0010g0177 a0001c0001t0027g0174 others(3): Show |
6 | 212 | 0.0283 | 3 | c.221 others(20): Show |
TIAM1 | ENSG00000156299.15 | transcript | ENST00000541036.6 | protein_coding | 10/27 | chr21 | TogoVar | |||||||
TIAM1_chr21_31113418_31349261 | 31210647 | A | AGGG | intron_variant | MODIFIER | HG00558.hp2 HG00738.hp1 HG01071.hp2 others(5): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0026others(3): Show | a0001c0001t0002a0001c0002t0001a0001c0002t0007others(4): Show | a0001c0001t0002g0119 a0001c0002t0001g0151 a0001c0002t0007g0083 others(5): Show |
8 | 212 | 0.0377 | 3 | c.221 others(20): Show |
TIAM1 | ENSG00000156299.15 | transcript | ENST00000541036.6 | protein_coding | 10/27 | chr21 | TogoVar | |||||||
TIAM1_chr21_31113418_31349261 | 31212606 | C | CTTT | intron_variant | MODIFIER | HG00621.hp2 HG01891.hp2 HG02451.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(4): Show | a0001c0001t0002g0118 a0001c0001t0006g0059 a0001c0001t0006g0060 others(9): Show |
12 | 212 | 0.0566 | 3 | c.221 others(20): Show |
TIAM1 | ENSG00000156299.15 | transcript | ENST00000541036.6 | protein_coding | 10/27 | chr21 | TogoVar | |||||||
TIAM1_chr21_31113418_31349261 | 31215568 | G | GAAA | intron_variant | MODIFIER | HG02451.hp1 HG02615.hp2 HG02895.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0006 | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(3): Show | a0001c0001t0002g0118 a0001c0001t0006g0059 a0001c0001t0006g0060 others(6): Show |
9 | 212 | 0.0425 | 3 | c.214 others(22): Show |
TIAM1 | ENSG00000156299.15 | transcript | ENST00000541036.6 | protein_coding | 9/27 | chr21 | TogoVar | |||||||
TIAM1_chr21_31113418_31349261 | 31215589 | A | AAAG | intron_variant | MODIFIER | HG02300.hp2 HG02647.hp2 HG02723.hp2 others(6): Show |
a0001a0003a0010 | a0001c0001a0003c0005a0003c0008others(1): Show | a0001c0001t0009a0003c0005t0001a0003c0005t0004others(5): Show | a0001c0001t0009g0122 a0003c0005t0001g0100 a0003c0005t0001g0185 others(6): Show |
9 | 212 | 0.0425 | 3 | c.214 others(22): Show |
TIAM1 | ENSG00000156299.15 | transcript | ENST00000541036.6 | protein_coding | 9/27 | chr21 | TogoVar | |||||||
TIAM1_chr21_31113418_31349261 | 31243207 | A | ATAT | intron_variant | MODIFIER | HG01952.hp1 HG02559.hp1 HG03669.hp1 others(2): Show |
a0001a0002a0003 | a0001c0002a0002c0004a0003c0005 | a0001c0002t0004a0002c0004t0001a0002c0004t0005others(1): Show | a0001c0002t0004g0092 a0001c0002t0004g0167 a0002c0004t0001g0089 others(2): Show |
5 | 212 | 0.0236 | 3 | c.158 others(22): Show |
TIAM1 | ENSG00000156299.15 | transcript | ENST00000541036.6 | protein_coding | 6/27 | chr21 | TogoVar | |||||||
TIAM1_chr21_31113418_31349261 | 31259629 | A | AAAT | intron_variant | MODIFIER | HG01496.hp1 HG01891.hp2 HG02602.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0008a0001c0001t0009a0001c0002t0001 | a0001c0001t0008g0169 a0001c0001t0009g0203 a0001c0002t0001g0116 others(2): Show |
5 | 212 | 0.0236 | 3 | c.963 others(20): Show |
TIAM1 | ENSG00000156299.15 | transcript | ENST00000541036.6 | protein_coding | 4/27 | chr21 | TogoVar | |||||||
TIAM1_chr21_31113418_31349261 | 31261262 | C | CTTT | intron_variant | MODIFIER | HG00735.hp2 HG01978.hp2 HG02738.hp1 others(2): Show |
a0001a0002 | a0001c0002a0002c0003a0002c0004 | a0001c0002t0001a0001c0002t0007a0002c0003t0002others(1): Show | a0001c0002t0001g0099 a0001c0002t0007g0082 a0001c0002t0007g0160 others(2): Show |
5 | 212 | 0.0236 | 3 | c.963 others(20): Show |
TIAM1 | ENSG00000156299.15 | transcript | ENST00000541036.6 | protein_coding | 4/27 | chr21 | TogoVar |