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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TG_chr8_132861958_133139899 | 132901152 | G | GGA | intron_variant | MODIFIER | HG02622.hp2 HG02630.hp2 HG02818.hp2 others(4): Show |
a0027a0028a0099others(2): Show | a0027c0030a0028c0029a0099c0137others(2): Show | a0027c0030t0001a0028c0029t0001a0099c0137t0001others(2): Show | a0027c0030t0001g0209a0027c0030t0001g0210a0028c0029t0001g0205others(4): Show | 7 | 216 | 0.0324 | 2 | c.343 others(19): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 15/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132917388 | A | ATG | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(46): Show |
a0004a0005a0006others(20): Show | a0004c0004a0005c0003a0006c0006others(22): Show | a0004c0004t0001a0005c0003t0001a0006c0006t0001others(22): Show | a0004c0004t0001g0165a0004c0004t0001g0167a0004c0004t0001g0173others(46): Show | 49 | 216 | 0.2269 | 2 | c.437 others(21): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 20/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132917889 | A | ATT | intron_variant | MODIFIER | HG00639.hp2 HG01106.hp2 HG01358.hp1 others(26): Show |
a0001a0002a0008others(22): Show | a0001c0112a0002c0001a0008c0007others(24): Show | a0001c0112t0001a0002c0001t0001a0008c0007t0001others(24): Show | a0001c0112t0001g0199a0002c0001t0001g0189a0008c0007t0001g0097others(26): Show | 29 | 216 | 0.1343 | 2 | c.437 others(21): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 20/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132925516 | C | CGT | intron_variant | MODIFIER | HG00544.hp1 HG01099.hp1 HG01106.hp2 others(54): Show |
a0001a0002a0008others(38): Show | a0001c0002a0002c0001a0002c0143others(39): Show | a0001c0002t0001a0002c0001t0001a0002c0143t0001others(39): Show | a0001c0002t0001g0059a0002c0001t0001g0010a0002c0001t0001g0092others(54): Show | 57 | 216 | 0.2639 | 2 | c.469 others(21): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 22/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132929620 | T | TAA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(47): Show |
a0004a0005a0006others(20): Show | a0004c0004a0005c0003a0006c0006others(22): Show | a0004c0004t0001a0005c0003t0001a0006c0006t0001others(22): Show | a0004c0004t0001g0165a0004c0004t0001g0167a0004c0004t0001g0173others(47): Show | 50 | 216 | 0.2315 | 2 | c.481 others(19): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 23/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132933434 | T | TTG | intron_variant | MODIFIER | HG01081.hp1 HG01255.hp1 HG02280.hp1 others(7): Show |
a0002a0004a0005others(7): Show | a0002c0143a0004c0004a0005c0003others(7): Show | a0002c0143t0001a0004c0004t0001a0005c0003t0001others(7): Show | a0002c0143t0001g0095a0004c0004t0001g0178a0005c0003t0001g0182others(7): Show | 10 | 216 | 0.0463 | 2 | c.481 others(17): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 23/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132939045 | C | CAA | intron_variant | MODIFIER | HG02622.hp2 HG02630.hp2 HG02723.hp1 others(6): Show |
a0027a0028a0070others(4): Show | a0027c0030a0028c0029a0070c0068others(4): Show | a0027c0030t0001a0028c0029t0001a0070c0068t0001others(4): Show | a0027c0030t0001g0209a0027c0030t0001g0210a0028c0029t0001g0205others(6): Show | 9 | 216 | 0.0417 | 2 | c.504 others(21): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 25/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132957742 | T | TAC | intron_variant | MODIFIER | HG00741.hp1 HG01361.hp1 HG02970.hp2 others(4): Show |
a0001a0003a0014others(3): Show | a0001c0002a0003c0005a0003c0104others(4): Show | a0001c0002t0001a0003c0005t0001a0003c0104t0001others(4): Show | a0001c0002t0001g0068a0003c0005t0001g0071a0003c0104t0001g0051others(4): Show | 7 | 216 | 0.0324 | 2 | c.540 others(21): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 27/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132957766 | C | CAG | intron_variant | MODIFIER | HG01106.hp2 HG02145.hp1 HG02257.hp2 others(25): Show |
a0013a0022a0023others(21): Show | a0013c0010a0022c0065a0022c0066others(22): Show | a0013c0010t0001a0022c0065t0001a0022c0066t0001others(22): Show | a0013c0010t0001g0014a0013c0010t0001g0015a0013c0010t0001g0016others(25): Show | 28 | 216 | 0.1296 | 2 | c.540 others(21): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 27/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132958683 | A | ACT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(182): Show |
a0001a0002a0003others(114): Show | a0001c0002a0001c0112a0002c0001others(126): Show | a0001c0002t0001a0001c0112t0001a0002c0001t0001others(126): Show | a0001c0002t0001g0019a0001c0002t0001g0040a0001c0002t0001g0059others(182): Show | 185 | 216 | 0.8565 | 2 | c.540 others(21): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 27/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132958710 | C | CAA | intron_variant | MODIFIER | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(52): Show |
a0001a0013a0017others(44): Show | a0001c0112a0013c0010a0017c0099others(45): Show | a0001c0112t0001a0013c0010t0001a0017c0099t0001others(45): Show | a0001c0112t0001g0199a0013c0010t0001g0014a0013c0010t0001g0015others(52): Show | 55 | 216 | 0.2546 | 2 | c.540 others(21): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 27/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132963670 | A | AGT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(46): Show |
a0001a0004a0005others(23): Show | a0001c0002a0004c0004a0005c0003others(25): Show | a0001c0002t0001a0004c0004t0001a0005c0003t0001others(25): Show | a0001c0002t0001g0058a0004c0004t0001g0167a0004c0004t0001g0173others(46): Show | 49 | 216 | 0.2269 | 2 | c.554 others(19): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132966462 | C | CTG | intron_variant | MODIFIER | HG01934.hp2 HG02055.hp2 |
a0001a0004 | a0001c0112a0004c0004 | a0001c0112t0001a0004c0004t0001 | a0001c0112t0001g0199a0004c0004t0001g0184 | 2 | 216 | 0.0093 | 2 | c.554 others(17): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132966464 | C | CTG | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(41): Show |
a0004a0005a0006others(20): Show | a0004c0004a0005c0003a0006c0006others(22): Show | a0004c0004t0001a0005c0003t0001a0006c0006t0001others(22): Show | a0004c0004t0001g0165a0004c0004t0001g0167a0004c0004t0001g0173others(41): Show | 44 | 216 | 0.2037 | 2 | c.554 others(17): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132966466 | C | CTG | intron_variant | MODIFIER | NA18957.hp1 homoSapiens_chm13v2.hp1 |
a0001a0103 | a0001c0002a0103c0124 | a0001c0002t0001a0103c0124t0001 | a0001c0002t0001g0073a0103c0124t0001g0057 | 2 | 216 | 0.0093 | 2 | c.554 others(17): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 29/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132972569 | G | GTT | intron_variant | MODIFIER | HG00140.hp2 HG00642.hp1 HG01099.hp1 others(14): Show |
a0003a0017a0023others(14): Show | a0003c0005a0017c0099a0023c0046others(14): Show | a0003c0005t0001a0017c0099t0001a0023c0046t0001others(14): Show | a0003c0005t0001g0026a0017c0099t0001g0065a0023c0046t0001g0134others(14): Show | 17 | 216 | 0.0787 | 2 | c.605 others(17): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 33/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132986410 | G | GTA | intron_variant | MODIFIER | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(105): Show |
a0001a0002a0003others(85): Show | a0001c0002a0001c0112a0002c0001others(93): Show | a0001c0002t0001a0001c0112t0001a0002c0001t0001others(93): Show | a0001c0002t0001g0073a0001c0112t0001g0199a0002c0001t0001g0091others(105): Show | 108 | 216 | 0.5000 | 2 | c.626 others(21): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 35/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132987721 | G | GGT | intron_variant | MODIFIER | HG00140.hp2 HG00642.hp1 HG00642.hp2 others(91): Show |
a0001a0002a0003others(73): Show | a0001c0112a0002c0001a0003c0005others(79): Show | a0001c0112t0001a0002c0001t0001a0003c0005t0001others(79): Show | a0001c0112t0001g0199a0002c0001t0001g0091a0003c0005t0001g0026others(91): Show | 94 | 216 | 0.4352 | 2 | c.626 others(21): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 35/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132988064 | G | GCA | intron_variant | MODIFIER | HG00099.hp1 HG00621.hp2 HG00639.hp1 others(32): Show |
a0001a0002a0004others(28): Show | a0001c0002a0002c0001a0004c0004others(29): Show | a0001c0002t0001a0002c0001t0001a0004c0004t0001others(29): Show | a0001c0002t0001g0040a0002c0001t0001g0189a0004c0004t0001g0178others(32): Show | 35 | 216 | 0.1620 | 2 | c.626 others(21): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 35/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132990158 | T | TTA | intron_variant | MODIFIER | HG00621.hp1 HG00642.hp2 HG01123.hp2 others(32): Show |
a0002a0005a0010others(27): Show | a0002c0001a0005c0003a0010c0008others(28): Show | a0002c0001t0001a0005c0003t0001a0010c0008t0001others(28): Show | a0002c0001t0001g0091a0005c0003t0001g0150a0010c0008t0001g0102others(32): Show | 35 | 216 | 0.1620 | 2 | c.626 others(21): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 35/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 132990915 | G | GTT | intron_variant | MODIFIER | HG00621.hp1 HG02280.hp2 HG02486.hp1 others(3): Show |
a0005a0018a0020others(3): Show | a0005c0003a0018c0013a0020c0020others(3): Show | a0005c0003t0001a0018c0013t0001a0020c0020t0001others(3): Show | a0005c0003t0001g0150a0018c0013t0001g0039a0020c0020t0001g0086others(3): Show | 6 | 216 | 0.0278 | 2 | c.626 others(21): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 35/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 133039953 | G | GCA | intron_variant | MODIFIER | HG00639.hp2 HG01884.hp2 HG02055.hp1 others(42): Show |
a0001a0003a0007others(33): Show | a0001c0113a0003c0005a0007c0009others(38): Show | a0001c0113t0001a0003c0005t0001a0007c0009t0001others(38): Show | a0001c0113t0001g0048a0003c0005t0001g0036a0007c0009t0001g0027others(42): Show | 45 | 216 | 0.2083 | 2 | c.723 others(21): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 41/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 133041784 | G | GTT | intron_variant | MODIFIER | HG01934.hp1 HG02258.hp2 HG02559.hp2 others(5): Show |
a0012a0055a0085others(5): Show | a0012c0067a0055c0090a0085c0035others(5): Show | a0012c0067t0001a0055c0090t0001a0085c0035t0001others(5): Show | a0012c0067t0001g0107a0055c0090t0001g0132a0085c0035t0001g0126others(5): Show | 8 | 216 | 0.0370 | 2 | c.723 others(23): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 41/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 133042678 | C | CTT | intron_variant | MODIFIER | HG00099.hp2 HG00642.hp1 HG01943.hp1 others(6): Show |
a0002a0024a0070others(6): Show | a0002c0001a0024c0017a0070c0068others(6): Show | a0002c0001t0001a0024c0017t0001a0070c0068t0001others(6): Show | a0002c0001t0001g0106a0024c0017t0001g0127a0070c0068t0001g0140others(6): Show | 9 | 216 | 0.0417 | 2 | c.723 others(23): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 41/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 133055363 | G | GCA | intron_variant | MODIFIER | HG01099.hp2 HG03209.hp2 HG03710.hp2 others(3): Show |
a0003a0007a0018others(2): Show | a0003c0005a0007c0009a0018c0013others(2): Show | a0003c0005t0001a0007c0009t0001a0018c0013t0001others(2): Show | a0003c0005t0001g0023a0003c0005t0001g0071a0007c0009t0001g0037others(3): Show | 6 | 216 | 0.0278 | 2 | c.723 others(23): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 41/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 133057774 | C | CAA | intron_variant | MODIFIER | HG00140.hp2 HG01106.hp1 HG01168.hp1 others(23): Show |
a0011a0012a0014others(16): Show | a0011c0011a0012c0067a0014c0023others(17): Show | a0011c0011t0001a0012c0067t0001a0014c0023t0001others(17): Show | a0011c0011t0001g0093a0011c0011t0001g0141a0011c0011t0001g0158others(23): Show | 26 | 216 | 0.1204 | 2 | c.723 others(23): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 41/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 133066325 | C | CAA | intron_variant | MODIFIER | HG00621.hp2 HG00639.hp2 HG01106.hp2 others(63): Show |
a0001a0004a0007others(38): Show | a0001c0002a0004c0004a0007c0009others(43): Show | a0001c0002t0001a0004c0004t0001a0007c0009t0001others(43): Show | a0001c0002t0001g0019a0001c0002t0001g0040a0001c0002t0001g0058others(63): Show | 66 | 216 | 0.3056 | 2 | c.724 others(23): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 41/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 133069501 | T | TTG | intron_variant | MODIFIER | HG02258.hp1 HG02559.hp2 HG02615.hp1 others(18): Show |
a0007a0012a0023others(15): Show | a0007c0009a0007c0125a0012c0048others(17): Show | a0007c0009t0001a0007c0125t0001a0012c0048t0001others(17): Show | a0007c0009t0001g0027a0007c0009t0001g0028a0007c0125t0001g0035others(18): Show | 21 | 216 | 0.0972 | 2 | c.724 others(23): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 41/47 | chr8 | TogoVar | ||||||
TG_chr8_132861958_133139899 | 133070029 | A | AAC | intron_variant | MODIFIER | HG00544.hp1 HG02630.hp2 HG02809.hp1 others(4): Show |
a0007a0015a0026others(4): Show | a0007c0009a0015c0114a0026c0016others(4): Show | a0007c0009t0001a0015c0114t0001a0026c0016t0001others(4): Show | a0007c0009t0001g0027a0015c0114t0001g0049a0026c0016t0001g0213others(4): Show | 7 | 216 | 0.0324 | 2 | c.724 others(23): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 41/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 133076759 | T | TAA | intron_variant | MODIFIER | HG00642.hp2 HG01243.hp2 HG01884.hp2 others(11): Show |
a0015a0027a0031others(9): Show | a0015c0024a0015c0114a0027c0030others(10): Show | a0015c0024t0001a0015c0114t0001a0027c0030t0001others(10): Show | a0015c0024t0001g0046a0015c0114t0001g0049a0027c0030t0001g0210others(11): Show | 14 | 216 | 0.0648 | 2 | c.724 others(23): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 41/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 133076759 | T | TTA | intron_variant | MODIFIER | HG01358.hp1 HG01433.hp2 HG01517.hp2 |
a0017a0124 | a0017c0025a0124c0129 | a0017c0025t0001a0124c0129t0001 | a0017c0025t0001g0020a0017c0025t0001g0021a0124c0129t0001g0038 | 3 | 216 | 0.0139 | 2 | c.724 others(23): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 41/47 | chr8 | TogoVar | ||||||
TG_chr8_132861958_133139899 | 133077735 | A | ATG | intron_variant | MODIFIER | HG02976.hp2 HG03540.hp2 NA20129.hp2 |
a0023a0045a0059 | a0023c0061a0045c0036a0059c0085 | a0023c0061t0001a0045c0036t0001a0059c0085t0001 | a0023c0061t0001g0139a0045c0036t0001g0001a0059c0085t0001g0008 | 3 | 216 | 0.0139 | 2 | c.724 others(23): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 41/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 133093104 | A | AGT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(24): Show |
a0011a0012a0014others(16): Show | a0011c0011a0012c0067a0014c0023others(18): Show | a0011c0011t0001a0012c0067t0001a0014c0023t0001others(18): Show | a0011c0011t0001g0141a0011c0011t0001g0158a0012c0067t0001g0107others(24): Show | 27 | 216 | 0.1250 | 2 | c.724 others(21): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 41/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 133094242 | C | CTT | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG01106.hp1 others(24): Show |
a0011a0012a0014others(16): Show | a0011c0011a0012c0067a0014c0023others(18): Show | a0011c0011t0001a0012c0067t0001a0014c0023t0001others(18): Show | a0011c0011t0001g0093a0011c0011t0001g0141a0011c0011t0001g0158others(24): Show | 27 | 216 | 0.1250 | 2 | c.724 others(19): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 41/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 133128337 | G | GCA | intron_variant | MODIFIER | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(24): Show |
a0001a0002a0003others(19): Show | a0001c0002a0002c0001a0003c0005others(20): Show | a0001c0002t0001a0002c0001t0001a0003c0005t0001others(20): Show | a0001c0002t0001g0040a0001c0002t0001g0059a0002c0001t0001g0092others(24): Show | 27 | 216 | 0.1250 | 2 | c.786 others(21): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 45/47 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
TG_chr8_132861958_133139899 | 133136244 | C | CTT | downstream_gene_variant | MODIFIER | HG00621.hp2 HG00642.hp1 HG00741.hp1 others(33): Show |
a0001a0003a0004others(19): Show | a0001c0002a0003c0104a0004c0004others(19): Show | a0001c0002t0001a0003c0104t0001a0004c0004t0001others(19): Show | a0001c0002t0001g0019a0001c0002t0001g0040a0001c0002t0001g0058others(33): Show | 36 | 216 | 0.1667 | 2 | c.*14 others(13): Show |
TG | ENSG00000042832.12 | transcript | ENST00000220616.9 | protein_coding | 1346 | chr8 | TogoVar | ||||||
THADA_chr2_43225851_43601038 | 43229795 | T | TGA | downstream_gene_variant | MODIFIER | HG00642.hp1 HG01099.hp1 HG02965.hp2 others(3): Show |
a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0115a0001c0006t0001g0116a0001c0006t0001g0157others(3): Show | 6 | 206 | 0.0291 | 2 | c.*11 others(13): Show |
THADA | ENSG00000115970.19 | transcript | ENST00000405975.7 | protein_coding | 1055 | chr2 | TogoVar | ||||||
THADA_chr2_43225851_43601038 | 43229819 | A | AGT | downstream_gene_variant | MODIFIER | HG01255.hp2 HG02723.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0056a0002c0002t0001g0181 | 2 | 206 | 0.0097 | 2 | c.*11 others(13): Show |
THADA | ENSG00000115970.19 | transcript | ENST00000405975.7 | protein_coding | 1031 | chr2 | TogoVar | ||||||
THADA_chr2_43225851_43601038 | 43236905 | C | CAA | intron_variant | MODIFIER | HG01243.hp1 HG01346.hp2 HG01981.hp1 others(16): Show |
a0001a0003a0004others(3): Show | a0001c0001a0003c0003a0003c0009others(5): Show | a0001c0001t0001a0003c0003t0001a0003c0009t0001others(5): Show | a0001c0001t0001g0054a0001c0001t0001g0072a0001c0001t0001g0165others(16): Show | 19 | 206 | 0.0922 | 2 | c.529 others(21): Show |
THADA | ENSG00000115970.19 | transcript | ENST00000405975.7 | protein_coding | 36/37 | chr2 | TogoVar | ||||||
THADA_chr2_43225851_43601038 | 43237397 | A | ATT | intron_variant | MODIFIER | HG00642.hp1 HG00642.hp2 HG02056.hp2 others(5): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0006a0002c0002others(3): Show | a0001c0001t0001a0001c0006t0001a0002c0002t0001others(3): Show | a0001c0001t0001g0046a0001c0006t0001g0158a0002c0002t0001g0188others(5): Show | 8 | 206 | 0.0388 | 2 | c.529 others(21): Show |
THADA | ENSG00000115970.19 | transcript | ENST00000405975.7 | protein_coding | 36/37 | chr2 | TogoVar | ||||||
THADA_chr2_43225851_43601038 | 43238118 | C | CAA | intron_variant | MODIFIER | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(19): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0001a0002c0002t0001a0003c0003t0001others(1): Show | a0001c0001t0001g0055a0001c0001t0001g0062a0001c0001t0001g0079others(19): Show | 22 | 206 | 0.1068 | 2 | c.529 others(21): Show |
THADA | ENSG00000115970.19 | transcript | ENST00000405975.7 | protein_coding | 36/37 | chr2 | TogoVar | ||||||
THADA_chr2_43225851_43601038 | 43247727 | C | CAA | intron_variant | MODIFIER | HG02074.hp2 HG02258.hp1 HG03490.hp2 others(3): Show |
a0001a0002a0004others(2): Show | a0001c0001a0002c0002a0004c0005others(2): Show | a0001c0001t0001a0002c0002t0001a0004c0005t0001others(2): Show | a0001c0001t0001g0051a0001c0001t0001g0053a0002c0002t0001g0172others(3): Show | 6 | 206 | 0.0291 | 2 | c.529 others(23): Show |
THADA | ENSG00000115970.19 | transcript | ENST00000405975.7 | protein_coding | 36/37 | chr2 | TogoVar | ||||||
THADA_chr2_43225851_43601038 | 43248130 | A | AAT | intron_variant | MODIFIER | HG02055.hp1 HG02647.hp2 HG03130.hp2 others(2): Show |
a0001a0002a0007others(1): Show | a0001c0001a0002c0002a0007c0014others(1): Show | a0001c0001t0001a0002c0002t0001a0007c0014t0002others(1): Show | a0001c0001t0001g0103a0002c0002t0001g0198a0002c0002t0001g0205others(2): Show | 5 | 206 | 0.0243 | 2 | c.529 others(23): Show |
THADA | ENSG00000115970.19 | transcript | ENST00000405975.7 | protein_coding | 36/37 | chr2 | TogoVar | ||||||
THADA_chr2_43225851_43601038 | 43248162 | T | TAG | intron_variant | MODIFIER | HG00621.hp1 HG00735.hp2 HG01192.hp2 others(1): Show |
a0001a0003a0007others(1): Show | a0001c0001a0003c0003a0007c0007others(1): Show | a0001c0001t0001a0003c0003t0001a0007c0007t0002others(1): Show | a0001c0001t0001g0123a0003c0003t0001g0130a0007c0007t0002g0003others(1): Show | 4 | 206 | 0.0194 | 2 | c.529 others(23): Show |
THADA | ENSG00000115970.19 | transcript | ENST00000405975.7 | protein_coding | 36/37 | chr2 | TogoVar | ||||||
THADA_chr2_43225851_43601038 | 43248164 | T | TAG | intron_variant | MODIFIER | HG01496.hp1 HG02056.hp1 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0001a0003c0003t0001 | a0001c0001t0001g0077a0003c0003t0001g0129 | 2 | 206 | 0.0097 | 2 | c.529 others(23): Show |
THADA | ENSG00000115970.19 | transcript | ENST00000405975.7 | protein_coding | 36/37 | chr2 | TogoVar | ||||||
THADA_chr2_43225851_43601038 | 43248232 | C | CAG | intron_variant | MODIFIER | HG00642.hp1 HG00738.hp2 HG01099.hp1 others(7): Show |
a0001a0011 | a0001c0001a0001c0006a0011c0028 | a0001c0001t0001a0001c0006t0001a0011c0028t0001 | a0001c0001t0001g0084a0001c0001t0001g0110a0001c0001t0001g0118others(7): Show | 10 | 206 | 0.0485 | 2 | c.529 others(23): Show |
THADA | ENSG00000115970.19 | transcript | ENST00000405975.7 | protein_coding | 36/37 | chr2 | TogoVar | ||||||
THADA_chr2_43225851_43601038 | 43256612 | A | ACT | intron_variant | MODIFIER | HG02622.hp1 HG02886.hp1 HG02895.hp2 others(6): Show |
a0006a0011a0022others(1): Show | a0006c0008a0011c0028a0022c0025others(1): Show | a0006c0008t0001a0011c0028t0001a0022c0025t0001others(1): Show | a0006c0008t0001g0047a0006c0008t0001g0048a0006c0008t0001g0057others(6): Show | 9 | 206 | 0.0437 | 2 | c.529 others(23): Show |
THADA | ENSG00000115970.19 | transcript | ENST00000405975.7 | protein_coding | 36/37 | chr2 | TogoVar | ||||||
THADA_chr2_43225851_43601038 | 43261216 | C | CTT | intron_variant | MODIFIER | HG00738.hp2 HG02055.hp1 HG02145.hp1 others(11): Show |
a0001a0003a0006others(4): Show | a0001c0001a0003c0003a0003c0009others(6): Show | a0001c0001t0001a0003c0003t0001a0003c0009t0001others(6): Show | a0001c0001t0001g0110a0001c0001t0001g0117a0001c0001t0001g0118others(11): Show | 14 | 206 | 0.0680 | 2 | c.529 others(23): Show |
THADA | ENSG00000115970.19 | transcript | ENST00000405975.7 | protein_coding | 36/37 | chr2 | TogoVar | ||||||
THADA_chr2_43225851_43601038 | 43274993 | C | CTT | intron_variant | MODIFIER | HG02559.hp2 HG03195.hp2 HG03540.hp2 |
a0004a0010a0019 | a0004c0005a0010c0013a0019c0033 | a0004c0005t0001a0010c0013t0001a0019c0033t0001 | a0004c0005t0001g0026a0010c0013t0001g0013a0019c0033t0001g0125 | 3 | 206 | 0.0146 | 2 | c.529 others(21): Show |
THADA | ENSG00000115970.19 | transcript | ENST00000405975.7 | protein_coding | 36/37 | chr2 | TogoVar | ||||||
THADA_chr2_43225851_43601038 | 43277951 | C | CTT | intron_variant | MODIFIER | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(46): Show |
a0001a0004a0005others(10): Show | a0001c0001a0001c0006a0001c0020others(18): Show | a0001c0001t0001a0001c0006t0001a0001c0020t0001others(18): Show | a0001c0001t0001g0110a0001c0001t0001g0117a0001c0001t0001g0118others(46): Show | 49 | 206 | 0.2379 | 2 | c.529 others(21): Show |
THADA | ENSG00000115970.19 | transcript | ENST00000405975.7 | protein_coding | 36/37 | chr2 | TogoVar |