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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ADAM23_chr2_206438532_206626127 | 206596899 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(50): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0017a0001c0001t0018others(3): Show | a0001c0001t0001g0004 a0001c0001t0001g0052 a0001c0001t0001g0059 others(49): Show |
53 | 130 | 0.4077 | -2 | c.235 others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206625409 | CGT | C | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(85): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0026others(11): Show | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0088 others(83): Show |
88 | 335 | 0.2627 | -2 | c.*77 others(13): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4283 | chr2 | TogoVar | |||||||
ADAM28_chr8_24289069_24364014 | 24289139 | TAG | T | upstream_gene_variant | MODIFIER | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(48): Show |
a0001a0002a0003others(2): Show | a0001c0002a0001c0034a0002c0003others(3): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(11): Show | a0001c0002t0001g0003 a0001c0002t0001g0280 a0001c0002t0001g0283 others(42): Show |
51 | 340 | 0.1500 | -2 | c.-50 others(13): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 4929 | chr8 | TogoVar | |||||||
ADAM28_chr8_24289069_24364014 | 24292834 | AGG | A | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(57): Show |
a0001a0002a0003others(3): Show | a0001c0002a0001c0034a0002c0003others(4): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(13): Show | a0001c0002t0001g0003 a0001c0002t0001g0280 a0001c0002t0001g0283 others(48): Show |
60 | 346 | 0.1734 | -2 | c.-13 others(13): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1234 | chr8 | TogoVar | |||||||
ADAM28_chr8_24289069_24364014 | 24299031 | GAA | G | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(9): Show |
a0001a0003a0009others(1): Show | a0001c0025a0003c0005a0009c0010others(2): Show | a0001c0025t0042a0003c0005t0005a0003c0005t0006others(3): Show | a0001c0025t0042g0248 a0003c0005t0005g0018 a0003c0005t0006g0240 others(8): Show |
12 | 337 | 0.0356 | -2 | c.47- others(15): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM28_chr8_24289069_24364014 | 24300130 | CAT | C | intron_variant | MODIFIER | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
a0005 | a0005c0008 | a0005c0008t0002 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | 346 | 0.0116 | -2 | c.150 others(15): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM28_chr8_24289069_24364014 | 24314924 | CAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(88): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0017others(9): Show | a0001c0001t0002a0001c0001t0044a0001c0002t0001others(28): Show | a0001c0001t0002g0227 a0001c0001t0044g0228 a0001c0002t0001g0003 others(76): Show |
91 | 300 | 0.3033 | -2 | c.576 others(19): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM28_chr8_24289069_24364014 | 24319495 | CAT | C | intron_variant | MODIFIER | HG03225.hp2 NA18906.hp1 NA20300.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 a0001c0001t0001g0048 |
3 | 346 | 0.0087 | -2 | c.577 others(17): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | TogoVar | |||||||
ADAM28_chr8_24289069_24364014 | 24329830 | ACT | A | intron_variant | MODIFIER | HG03139.hp1 HG03486.hp1 NA19030.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0017 | a0001c0001t0001g0084 a0001c0001t0002g0089 a0001c0001t0017g0042 |
3 | 346 | 0.0087 | -2 | c.973 others(17): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM28_chr8_24289069_24364014 | 24329869 | TTG | T | intron_variant | MODIFIER | HG02809.hp1 HG02965.hp2 HG03491.hp2 |
a0001a0002 | a0001c0001a0002c0007 | a0001c0001t0003a0002c0007t0002a0002c0007t0026 | a0001c0001t0003g0204 a0002c0007t0002g0116 a0002c0007t0026g0065 |
3 | 344 | 0.0087 | -2 | c.973 others(15): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM28_chr8_24289069_24364014 | 24333983 | GTT | G | intron_variant | MODIFIER | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
a0005 | a0005c0008 | a0005c0008t0002 | a0005c0008t0002g0006 a0005c0008t0002g0316 |
4 | 346 | 0.0116 | -2 | c.137 others(21): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM28_chr8_24289069_24364014 | 24336039 | GGT | G | intron_variant | MODIFIER | HG01891.hp1 HG02055.hp1 HG02922.hp1 others(2): Show |
a0005a0011 | a0005c0008a0011c0032 | a0005c0008t0002a0011c0032t0033 | a0005c0008t0002g0006 a0005c0008t0002g0316 a0011c0032t0033g0247 |
5 | 342 | 0.0146 | -2 | c.156 others(19): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM28_chr8_24289069_24364014 | 24344724 | CTT | C | intron_variant | MODIFIER | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
a0002a0005a0008others(1): Show | a0002c0003a0002c0007a0002c0019others(7): Show | a0002c0003t0001a0002c0003t0002a0002c0003t0003others(18): Show | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | 346 | 0.1272 | -2 | c.199 others(21): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM28_chr8_24289069_24364014 | 24350864 | GTT | G | intron_variant | MODIFIER | HG00423.hp2 HG00639.hp2 HG00642.hp2 others(27): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0002c0003others(5): Show | a0001c0001t0004a0001c0001t0010a0001c0002t0004others(8): Show | a0001c0001t0004g0094 a0001c0001t0004g0115 a0001c0001t0004g0125 others(27): Show |
30 | 36 | 0.8333 | -2 | c.210 others(19): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM28_chr8_24289069_24364014 | 24357128 | ATT | A | 3_prime_UTR_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0002a0001c0013others(28): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(82): Show | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(306): Show |
336 | 346 | 0.9711 | -2 | c.*27 others(13): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 2727 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM28_chr8_24289069_24364014 | 24360901 | CTT | C | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
a0001a0002a0003others(15): Show | a0001c0001a0001c0002a0001c0013others(29): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(84): Show | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(308): Show |
338 | 346 | 0.9769 | -2 | c.*64 others(13): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1888 | chr8 | TogoVar | |||||||
ADAM29_chr4_174913358_174983180 | 174914128 | AAC | A | upstream_gene_variant | MODIFIER | HG00544.hp1 HG01069.hp2 HG01168.hp2 others(6): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0003a0002c0002t0001a0002c0002t0004others(1): Show | a0001c0001t0003g0013 a0001c0001t0003g0048 a0002c0002t0001g0020 others(5): Show |
9 | 323 | 0.0279 | -2 | c.-48 others(13): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4229 | chr4 | TogoVar | |||||||
ADAM29_chr4_174913358_174983180 | 174916376 | AAG | A | upstream_gene_variant | MODIFIER | HG01884.hp2 HG02486.hp2 HG03225.hp2 others(2): Show |
a0001a0002a0009 | a0001c0006a0002c0002a0009c0012 | a0001c0006t0002a0002c0002t0002a0009c0012t0014 | a0001c0006t0002g0033 a0001c0006t0002g0035 a0002c0002t0002g0031 others(2): Show |
5 | 328 | 0.0152 | -2 | c.-26 others(13): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1981 | chr4 | TogoVar | |||||||
ADAM29_chr4_174913358_174983180 | 174923523 | ATG | A | intron_variant | MODIFIER | HG00639.hp1 HG01884.hp2 HG02486.hp2 others(1): Show |
a0002a0004 | a0002c0002a0004c0004 | a0002c0002t0002a0004c0004t0002 | a0002c0002t0002g0031 a0002c0002t0002g0032 a0004c0004t0002g0228 others(1): Show |
4 | 327 | 0.0122 | -2 | c.-45 others(21): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ADAM29_chr4_174913358_174983180 | 174923525 | GTA | G | intron_variant | MODIFIER | HG00544.hp1 HG01168.hp1 HG01981.hp2 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0004a0001c0001t0006a0002c0002t0004 | a0001c0001t0004g0015 a0001c0001t0004g0085 a0001c0001t0006g0096 others(4): Show |
7 | 93 | 0.0753 | -2 | c.-45 others(21): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ADAM29_chr4_174913358_174983180 | 174925349 | ACT | A | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00639.hp2 others(37): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0010 | a0001c0001t0003a0002c0002t0003a0002c0002t0012others(1): Show | a0001c0001t0003g0006 a0001c0001t0003g0012 a0001c0001t0003g0013 others(33): Show |
40 | 328 | 0.1220 | -2 | c.-45 others(21): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ADAM29_chr4_174913358_174983180 | 174931816 | TCA | T | intron_variant | MODIFIER | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(82): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0009a0001c0016others(5): Show | a0001c0001t0002a0001c0009t0013a0001c0016t0002others(6): Show | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0025 others(65): Show |
85 | 226 | 0.3761 | -2 | c.-26 others(19): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ADAM29_chr4_174913358_174983180 | 174952350 | CCA | C | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(93): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0106 others(71): Show |
96 | 260 | 0.3692 | -2 | c.-18 others(23): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ADAM29_chr4_174913358_174983180 | 174959457 | CTG | C | intron_variant | MODIFIER | HG00639.hp1 HG01109.hp1 HG02572.hp1 others(13): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0006a0002c0002others(2): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0008others(4): Show | a0001c0001t0002g0175 a0001c0001t0002g0246 a0001c0001t0002g0252 others(12): Show |
16 | 219 | 0.0731 | -2 | c.-18 others(23): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ADAM29_chr4_174913358_174983180 | 174968771 | CCA | C | intron_variant | MODIFIER | HG00438.hp1 HG02647.hp1 HG02809.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0152 a0001c0001t0001g0215 a0001c0001t0002g0246 others(5): Show |
8 | 114 | 0.0702 | -2 | c.-18 others(21): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ADAM29_chr4_174913358_174983180 | 174979268 | CAG | C | downstream_gene_variant | MODIFIER | HG00621.hp1 HG00738.hp1 HG02622.hp2 others(17): Show |
a0001 | a0001c0001a0001c0006a0001c0013 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0115 others(16): Show |
20 | 218 | 0.0917 | -2 | c.*12 others(13): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1089 | chr4 | TogoVar | |||||||
ADAM2_chr8_39738735_39843227 | 39760882 | CAA | C | intron_variant | MODIFIER | HG01175.hp1 HG01952.hp1 HG02280.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005 a0001c0001t0001g0105 a0001c0001t0001g0109 others(3): Show |
7 | 99 | 0.0707 | -2 | c.161 others(19): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 15/20 | chr8 | TogoVar | |||||||
ADAM2_chr8_39738735_39843227 | 39763881 | CAA | C | intron_variant | MODIFIER | HG02559.hp1 HG02572.hp1 HG02896.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0030 others(4): Show |
7 | 328 | 0.0213 | -2 | c.150 others(21): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 14/20 | chr8 | TogoVar | |||||||
ADAM2_chr8_39738735_39843227 | 39767896 | TCA | T | intron_variant | MODIFIER | HG00733.hp2 HG01192.hp1 HG01884.hp1 others(34): Show |
a0001a0002a0007others(1): Show | a0001c0001a0001c0006a0001c0015others(3): Show | a0001c0001t0001a0001c0006t0001a0001c0015t0001others(3): Show | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 others(34): Show |
37 | 146 | 0.2534 | -2 | c.121 others(19): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 12/20 | chr8 | TogoVar | |||||||
ADAM2_chr8_39738735_39843227 | 39787542 | CTA | C | intron_variant | MODIFIER | HG01167.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0025 a0001c0001t0001g0250 a0001c0001t0001g0251 others(5): Show |
8 | 310 | 0.0258 | -2 | c.810 others(17): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | TogoVar | |||||||
ADAM2_chr8_39738735_39843227 | 39787581 | ATG | A | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(259): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0006a0001c0007others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(239): Show |
262 | 328 | 0.7988 | -2 | c.809 others(17): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 9/20 | chr8 | TogoVar | |||||||
ADAM2_chr8_39738735_39843227 | 39808189 | TAC | T | intron_variant | MODIFIER | HG02809.hp1 HG02886.hp1 HG03486.hp2 others(2): Show |
a0001a0007 | a0001c0001a0001c0015a0007c0004 | a0001c0001t0001a0001c0015t0001a0007c0004t0001 | a0001c0001t0001g0181 a0001c0001t0001g0290 a0001c0001t0001g0294 others(2): Show |
5 | 94 | 0.0532 | -2 | c.570 others(19): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 7/20 | chr8 | TogoVar | |||||||
ADAM2_chr8_39738735_39843227 | 39812825 | AAC | A | intron_variant | MODIFIER | HG00558.hp2 HG00597.hp1 HG02083.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(2): Show |
5 | 328 | 0.0152 | -2 | c.514 others(19): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 6/20 | chr8 | TogoVar | |||||||
ADAM2_chr8_39738735_39843227 | 39838718 | CAA | C | upstream_gene_variant | MODIFIER | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(87): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0006a0001c0018others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0006t0001others(4): Show | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0013 others(77): Show |
90 | 205 | 0.4390 | -2 | c.-53 others(11): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 492 | chr8 | TogoVar | |||||||
ADAM2_chr8_39738735_39843227 | 39841514 | CTT | C | upstream_gene_variant | MODIFIER | HG01891.hp1 HG02615.hp2 NA19030.hp1 |
a0001a0006 | a0001c0001a0006c0005 | a0001c0001t0001a0006c0005t0001 | a0001c0001t0001g0071 a0006c0005t0001g0008 |
3 | 328 | 0.0091 | -2 | c.-33 others(13): Show |
ADAM2 | ENSG00000104755.16 | transcript | ENST00000265708.9 | protein_coding | 3288 | chr8 | TogoVar | |||||||
ADAM30_chr1_119888533_119901515 | 119890475 | CAT | C | downstream_gene_variant | MODIFIER | NA18986.hp1 NA18998.hp2 NA19082.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | 3 | 293 | 0.0102 | -2 | c.*34 others(13): Show |
ADAM30 | ENSG00000134249.7 | transcript | ENST00000369400.2 | protein_coding | 3057 | chr1 | TogoVar | |||||||
ADAM30_chr1_119888533_119901515 | 119892944 | CAA | C | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0005others(5): Show | a0001c0001t0001a0001c0003t0001a0001c0005t0001others(5): Show | a0001c0001t0001g0000 a0001c0003t0001g0000 a0001c0005t0001g0000 others(5): Show |
194 | 239 | 0.8117 | -2 | c.*10 others(13): Show |
ADAM30 | ENSG00000134249.7 | transcript | ENST00000369400.2 | protein_coding | 588 | chr1 | TogoVar | |||||||
ADAM32_chr8_39102734_39289917 | 39103406 | ATT | A | upstream_gene_variant | MODIFIER | HG02717.hp1 HG02895.hp1 HG02897.hp1 |
a0003 | a0003c0004 | a0003c0004t0001 | a0003c0004t0001g0135 a0003c0004t0001g0139 a0003c0004t0001g0140 |
3 | 256 | 0.0117 | -2 | c.-43 others(13): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 4327 | chr8 | TogoVar | |||||||
ADAM32_chr8_39102734_39289917 | 39111720 | CAA | C | intron_variant | MODIFIER | HG01516.hp2 HG02056.hp1 HG02273.hp2 others(10): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(2): Show | a0001c0001t0001g0160 a0001c0001t0001g0179 a0001c0001t0001g0180 others(10): Show |
13 | 26 | 0.5000 | -2 | c.58+ others(17): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39124414 | CTT | C | intron_variant | MODIFIER | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(54): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0002a0002c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(5): Show | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0147 others(53): Show |
57 | 63 | 0.9048 | -2 | c.138 others(19): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39129125 | CTT | C | intron_variant | MODIFIER | HG01943.hp1 HG02559.hp1 HG02717.hp2 others(6): Show |
a0001a0004a0006others(1): Show | a0001c0001a0004c0007a0006c0008others(1): Show | a0001c0001t0002a0004c0007t0001a0006c0008t0001others(2): Show | a0001c0001t0002g0019 a0004c0007t0001g0154 a0004c0007t0001g0155 others(6): Show |
9 | 55 | 0.1636 | -2 | c.139 others(19): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39160539 | CAA | C | intron_variant | MODIFIER | HG00438.hp2 HG00621.hp2 HG00738.hp1 others(47): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0003a0002c0005others(2): Show | a0001c0001t0001a0001c0001t0002a0002c0003t0001others(4): Show | a0001c0001t0001g0005 a0001c0001t0001g0150 a0001c0001t0001g0161 others(47): Show |
50 | 52 | 0.9615 | -2 | c.526 others(17): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39161997 | ATT | A | intron_variant | MODIFIER | HG00423.hp2 HG00621.hp1 NA18993.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0233 a0001c0001t0002g0067 a0001c0001t0002g0089 |
3 | 256 | 0.0117 | -2 | c.594 others(19): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39162000 | TTA | T | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(154): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0002c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(11): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
157 | 179 | 0.8771 | -2 | c.594 others(19): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39188089 | CAT | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
a0001a0002a0007others(2): Show | a0001c0001a0001c0002a0002c0003others(4): Show | a0001c0001t0002a0001c0002t0001a0001c0002t0002others(6): Show | a0001c0001t0002g0030 a0001c0001t0002g0127 a0001c0001t0002g0128 others(72): Show |
76 | 256 | 0.2969 | -2 | c.105 others(21): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39188668 | TAA | T | intron_variant | MODIFIER | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(7): Show |
a0003a0011 | a0003c0004a0011c0011 | a0003c0004t0001a0011c0011t0001 | a0003c0004t0001g0134 a0003c0004t0001g0135 a0003c0004t0001g0136 others(7): Show |
10 | 256 | 0.0391 | -2 | c.105 others(21): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 11/24 | chr8 | TogoVar | |||||||
ADAM32_chr8_39102734_39289917 | 39254298 | CTG | C | intron_variant | MODIFIER | HG01243.hp2 HG02055.hp2 HG02257.hp1 others(15): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0002a0002c0003t0001others(1): Show | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(15): Show |
18 | 256 | 0.0703 | -2 | c.190 others(19): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39271539 | CAA | C | intron_variant | MODIFIER | HG02027.hp1 HG02683.hp2 HG02723.hp1 others(3): Show |
a0001a0002a0005 | a0001c0002a0002c0005a0005c0006 | a0001c0002t0002a0002c0005t0002a0005c0006t0001 | a0001c0002t0002g0123 a0001c0002t0002g0130 a0002c0005t0002g0115 others(3): Show |
6 | 161 | 0.0373 | -2 | c.220 others(19): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39272101 | GAA | G | intron_variant | MODIFIER | HG01069.hp1 HG01943.hp2 HG02004.hp2 others(3): Show |
a0001a0002 | a0001c0002a0002c0003 | a0001c0002t0001a0001c0002t0002a0002c0003t0001 | a0001c0002t0001g0200 a0001c0002t0002g0096 a0001c0002t0002g0103 others(3): Show |
6 | 256 | 0.0234 | -2 | c.220 others(21): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39277054 | CTA | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(107): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0002c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(13): Show | a0001c0001t0001g0149 a0001c0001t0001g0177 a0001c0001t0001g0210 others(106): Show |
110 | 256 | 0.4297 | -2 | c.227 others(21): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar |