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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ADAM23_chr2_206438532_206626127 | 206515829 | G | GT | intron_variant | MODIFIER | HG02258.hp1 HG02451.hp2 HG02559.hp2 others(16): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008 | a0001c0001t0001g0181a0001c0001t0001g0308a0001c0001t0001g0309others(16): Show | 19 | 358 | 0.0531 | 1 | c.510 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206516324 | G | GT | intron_variant | MODIFIER | HG01884.hp1 HG02647.hp1 HG03927.hp2 others(2): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0005t0027 | a0001c0001t0001g0287a0001c0001t0001g0310a0001c0001t0002g0246others(2): Show | 5 | 358 | 0.0140 | 1 | c.510 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206522804 | A | AT | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0007others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(19): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(131): Show | 138 | 358 | 0.3855 | 1 | c.510 others(9): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206529819 | A | AT | intron_variant | MODIFIER | HG00280.hp2 HG00544.hp2 HG00642.hp1 others(64): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0007others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(11): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(62): Show | 67 | 358 | 0.1872 | 1 | c.510 others(9): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206530669 | C | CT | intron_variant | MODIFIER | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(13): Show | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0045others(74): Show | 79 | 358 | 0.2207 | 1 | c.510 others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206534481 | C | CT | intron_variant | MODIFIER | HG02055.hp1 HG02559.hp1 HG02647.hp2 others(4): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0015a0001c0002t0019 | a0001c0002t0001g0257a0001c0002t0001g0258a0001c0002t0001g0259others(4): Show | 7 | 358 | 0.0196 | 1 | c.573 others(9): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206534964 | C | CT | intron_variant | MODIFIER | HG00280.hp1 HG00738.hp2 HG01099.hp1 others(20): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0034a0001c0001t0035others(4): Show | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0034g0079others(19): Show | 23 | 358 | 0.0643 | 1 | c.573 others(9): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206550599 | C | CT | intron_variant | MODIFIER | HG02056.hp2 HG02109.hp2 HG02132.hp2 others(19): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(9): Show | a0001c0001t0001g0060a0001c0001t0001g0103a0001c0001t0001g0232others(19): Show | 22 | 358 | 0.0615 | 1 | c.933 others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206573624 | T | TA | intron_variant | MODIFIER | HG01261.hp1 HG02155.hp2 HG02257.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0003a0001c0002t0029 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0001g0203others(3): Show | 7 | 358 | 0.0196 | 1 | c.173 others(9): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206574402 | C | CT | intron_variant | MODIFIER | HG00673.hp2 HG02056.hp2 HG02071.hp2 others(40): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0006 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(5): Show | a0001c0001t0001g0064a0001c0001t0002g0233a0001c0002t0001g0150others(39): Show | 43 | 358 | 0.1201 | 1 | c.173 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206583678 | A | AT | intron_variant | MODIFIER | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0002a0001c0002t0011 | a0001c0002t0001g0092a0001c0002t0002g0302a0001c0002t0011g0186others(2): Show | 5 | 358 | 0.0140 | 1 | c.173 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206587580 | G | GA | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0007others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0012others(15): Show | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(121): Show | 126 | 358 | 0.3520 | 1 | c.178 others(9): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206596899 | C | CT | intron_variant | MODIFIER | HG01175.hp1 HG02109.hp2 HG02559.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0001t0034others(4): Show | a0001c0001t0002g0227a0001c0001t0002g0233a0001c0001t0002g0254others(7): Show | 10 | 358 | 0.0279 | 1 | c.235 others(9): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206597178 | C | CT | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(14): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(2): Show | a0001c0001t0001g0115a0001c0001t0001g0120a0001c0001t0001g0128others(14): Show | 17 | 358 | 0.0475 | 1 | c.235 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206599204 | C | CA | intron_variant | MODIFIER | HG02055.hp1 HG02155.hp2 HG02280.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0043others(3): Show | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0001t0001g0211others(10): Show | 13 | 358 | 0.0363 | 1 | c.235 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206601772 | C | CA | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0020 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0025others(9): Show | 13 | 358 | 0.0363 | 1 | c.235 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206603961 | C | CA | intron_variant | MODIFIER | HG02886.hp1 NA18973.hp2 NA18974.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0017a0001c0001t0037others(2): Show | a0001c0001t0001g0136a0001c0001t0017g0039a0001c0001t0037g0228others(4): Show | 7 | 358 | 0.0196 | 1 | c.236 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206607443 | T | TA | intron_variant | MODIFIER | HG02896.hp1 HG02897.hp1 HG03209.hp2 others(1): Show |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0011 | a0001c0002t0002g0302a0001c0002t0011g0186a0001c0002t0011g0187others(1): Show | 4 | 358 | 0.0112 | 1 | c.236 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206607882 | G | GT | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0007others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(28): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 200 | 358 | 0.5587 | 1 | c.236 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM28_chr8_24289069_24364014 | 24296312 | G | GT | intron_variant | MODIFIER | HG01261.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0019a0004c0004others(1): Show | a0001c0001t0002a0001c0001t0044a0002c0019t0006others(2): Show | a0001c0001t0002g0224a0001c0001t0002g0228a0001c0001t0002g0230others(4): Show | 7 | 348 | 0.0201 | 1 | c.46+ others(8): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM28_chr8_24289069_24364014 | 24299031 | G | GA | intron_variant | MODIFIER | HG02886.hp1 HG03486.hp1 HG03516.hp2 others(5): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0002a0001c0001t0003a0001c0001t0017others(2): Show | a0001c0001t0002g0091a0001c0001t0002g0137a0001c0001t0002g0224others(5): Show | 8 | 348 | 0.0230 | 1 | c.47- others(7): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM28_chr8_24289069_24364014 | 24302770 | C | CT | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG02145.hp2 others(8): Show |
a0003a0006a0011 | a0003c0005a0006c0010a0006c0028others(1): Show | a0003c0005t0005a0003c0005t0006a0006c0010t0002others(2): Show | a0003c0005t0005g0245a0003c0005t0005g0246a0003c0005t0006g0239others(8): Show | 11 | 348 | 0.0316 | 1 | c.150 others(9): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM28_chr8_24289069_24364014 | 24304916 | C | CA | intron_variant | MODIFIER | HG00621.hp2 HG01943.hp1 HG02071.hp2 others(38): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0003a0002c0031others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(15): Show | a0001c0001t0001g0032a0001c0001t0001g0075a0001c0001t0001g0143others(33): Show | 41 | 348 | 0.1178 | 1 | c.150 others(9): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM28_chr8_24289069_24364014 | 24305451 | C | CT | intron_variant | MODIFIER | HG00099.hp2 HG00738.hp2 HG01169.hp1 others(25): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0007a0003c0005others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0001g0070others(24): Show | 28 | 348 | 0.0805 | 1 | c.151 others(9): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM28_chr8_24289069_24364014 | 24312746 | C | CT | intron_variant | MODIFIER | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
a0005 | a0005c0008 | a0005c0008t0002 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | 348 | 0.0115 | 1 | c.384 others(8): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM28_chr8_24289069_24364014 | 24313758 | A | AT | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(59): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0017others(6): Show | a0001c0001t0002a0001c0001t0003a0001c0002t0001others(17): Show | a0001c0001t0002g0155a0001c0001t0003g0207a0001c0002t0001g0027others(57): Show | 62 | 348 | 0.1782 | 1 | c.576 others(8): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM28_chr8_24289069_24364014 | 24314924 | C | CA | intron_variant | MODIFIER | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(36): Show |
a0001a0004a0009others(1): Show | a0001c0001a0001c0025a0001c0026others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0094a0001c0001t0001g0096a0001c0001t0001g0112others(36): Show | 39 | 348 | 0.1121 | 1 | c.576 others(9): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM28_chr8_24289069_24364014 | 24316998 | A | AG | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(94): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0017others(11): Show | a0001c0001t0002a0001c0001t0044a0001c0002t0001others(30): Show | a0001c0001t0002g0228a0001c0001t0044g0227a0001c0002t0001g0027others(87): Show | 97 | 348 | 0.2787 | 1 | c.577 others(9): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM28_chr8_24289069_24364014 | 24325871 | C | CA | intron_variant | MODIFIER | HG00438.hp2 HG01081.hp1 HG01261.hp2 others(13): Show |
a0001a0002a0004 | a0001c0001a0002c0019a0004c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0042a0001c0001t0001g0076a0001c0001t0001g0087others(13): Show | 16 | 348 | 0.0460 | 1 | c.891 others(8): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM28_chr8_24289069_24364014 | 24328921 | C | CA | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(96): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0017others(10): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0001others(30): Show | a0001c0001t0001g0064a0001c0001t0001g0186a0001c0001t0004g0156others(89): Show | 99 | 348 | 0.2845 | 1 | c.973 others(9): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM28_chr8_24289069_24364014 | 24328929 | A | AG | intron_variant | MODIFIER | HG01891.hp1 HG02922.hp1 HG03195.hp1 others(1): Show |
a0005 | a0005c0008 | a0005c0008t0002 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | 348 | 0.0115 | 1 | c.973 others(18): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | chr8 | TogoVar | ||||||
ADAM28_chr8_24289069_24364014 | 24335166 | G | GT | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG01891.hp1 others(10): Show |
a0001a0003a0005others(1): Show | a0001c0001a0003c0005a0005c0008others(1): Show | a0001c0001t0044a0003c0005t0005a0003c0005t0006others(2): Show | a0001c0001t0044g0227a0003c0005t0005g0245a0003c0005t0005g0246others(10): Show | 13 | 348 | 0.0374 | 1 | c.137 others(9): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM28_chr8_24289069_24364014 | 24336580 | C | CA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(60): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0017others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | a0001c0001t0001g0026a0001c0001t0001g0062a0001c0001t0001g0186others(58): Show | 63 | 348 | 0.1810 | 1 | c.156 others(9): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM28_chr8_24289069_24364014 | 24343931 | A | AT | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
a0001a0002a0005others(5): Show | a0001c0001a0001c0002a0001c0034others(13): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0001others(33): Show | a0001c0001t0001g0062a0001c0001t0001g0186a0001c0001t0004g0156others(88): Show | 98 | 348 | 0.2816 | 1 | c.199 others(9): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM28_chr8_24289069_24364014 | 24345028 | C | CA | intron_variant | MODIFIER | HG01884.hp1 HG02109.hp2 HG02630.hp2 others(3): Show |
a0001a0004 | a0001c0001a0001c0025a0004c0004 | a0001c0001t0001a0001c0001t0002a0001c0025t0042others(1): Show | a0001c0001t0001g0073a0001c0001t0002g0108a0001c0001t0002g0137others(3): Show | 6 | 348 | 0.0172 | 1 | c.199 others(10): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM28_chr8_24289069_24364014 | 24353428 | A | AT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
a0001a0002a0003others(16): Show | a0001c0001a0001c0002a0001c0013others(29): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(80): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(313): Show | 334 | 348 | 0.9598 | 1 | c.224 others(9): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 21/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM28_chr8_24289069_24364014 | 24355517 | C | CT | 3_prime_UTR_variant | MODIFIER | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(24): Show |
a0001a0002a0017 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0004a0001c0001t0010a0001c0001t0012others(6): Show | a0001c0001t0004g0051a0001c0001t0004g0071a0001c0001t0004g0082others(24): Show | 27 | 348 | 0.0776 | 1 | c.*11 others(6): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 1125 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||
ADAM28_chr8_24289069_24364014 | 24358648 | C | CT | 3_prime_UTR_variant | MODIFIER | HG01109.hp1 HG01891.hp2 HG02004.hp2 others(23): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0013others(5): Show | a0001c0001t0005a0001c0001t0015a0001c0001t0017others(9): Show | a0001c0001t0005g0034a0001c0001t0005g0095a0001c0001t0005g0145others(23): Show | 26 | 348 | 0.0747 | 1 | c.*42 others(6): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 4250 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||
ADAM28_chr8_24289069_24364014 | 24360197 | C | CA | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
a0001a0002a0003others(16): Show | a0001c0001a0001c0002a0001c0013others(29): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(84): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(318): Show | 339 | 348 | 0.9741 | 1 | c.*57 others(12): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 1184 | chr8 | TogoVar | ||||||
ADAM29_chr4_174913358_174983180 | 174914166 | C | CG | upstream_gene_variant | MODIFIER | HG03139.hp2 HG03195.hp1 NA18964.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0005a0002c0002t0001 | a0001c0001t0001g0165a0001c0001t0005g0278a0001c0001t0005g0279others(1): Show | 4 | 330 | 0.0121 | 1 | c.-48 others(12): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4191 | chr4 | TogoVar | ||||||
ADAM29_chr4_174913358_174983180 | 174914169 | A | AG | upstream_gene_variant | MODIFIER | HG02572.hp1 HG03139.hp2 HG03195.hp1 others(2): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0004 | a0001c0001t0001a0001c0001t0005a0002c0002t0001others(1): Show | a0001c0001t0001g0165a0001c0001t0005g0278a0001c0001t0005g0279others(2): Show | 5 | 330 | 0.0152 | 1 | c.-48 others(12): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4188 | chr4 | TogoVar | ||||||
ADAM29_chr4_174913358_174983180 | 174916919 | T | TA | upstream_gene_variant | MODIFIER | HG01884.hp2 HG02486.hp2 HG02572.hp1 others(4): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0006a0002c0002others(2): Show | a0001c0001t0002a0001c0006t0002a0002c0002t0002others(2): Show | a0001c0001t0002g0035a0001c0006t0002g0032a0001c0006t0002g0033others(4): Show | 7 | 330 | 0.0212 | 1 | c.-21 others(12): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1438 | chr4 | TogoVar | ||||||
ADAM29_chr4_174913358_174983180 | 174918747 | T | TA | intron_variant | MODIFIER | HG00280.hp2 HG00642.hp2 HG00735.hp2 others(11): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0002c0002t0003a0002c0002t0012 | a0001c0001t0003g0008a0001c0001t0003g0009a0001c0001t0003g0040others(9): Show | 14 | 330 | 0.0424 | 1 | c.-55 others(9): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ADAM29_chr4_174913358_174983180 | 174926721 | C | CA | intron_variant | MODIFIER | HG01074.hp1 HG01934.hp1 HG02074.hp2 others(15): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0115a0001c0001t0001g0141a0001c0001t0001g0219others(14): Show | 18 | 330 | 0.0546 | 1 | c.-45 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ADAM29_chr4_174913358_174983180 | 174932297 | G | GA | intron_variant | MODIFIER | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(80): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0009a0001c0016others(6): Show | a0001c0001t0002a0001c0009t0013a0001c0016t0002others(7): Show | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0023others(64): Show | 83 | 330 | 0.2515 | 1 | c.-26 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ADAM29_chr4_174913358_174983180 | 174939097 | T | TA | intron_variant | MODIFIER | HG03041.hp1 HG03130.hp1 NA18522.hp2 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0008 | a0001c0001t0006g0073a0001c0001t0008g0099a0001c0001t0008g0100 | 3 | 330 | 0.0091 | 1 | c.-18 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ADAM29_chr4_174913358_174983180 | 174940514 | G | GA | intron_variant | MODIFIER | HG02630.hp2 HG02809.hp1 HG02886.hp1 others(4): Show |
a0001a0005 | a0001c0001a0005c0005a0005c0007 | a0001c0001t0002a0005c0005t0002a0005c0007t0002 | a0001c0001t0002g0233a0005c0005t0002g0022a0005c0005t0002g0231others(3): Show | 7 | 330 | 0.0212 | 1 | c.-18 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ADAM29_chr4_174913358_174983180 | 174942562 | T | TG | intron_variant | MODIFIER | HG01884.hp2 HG02258.hp1 HG02451.hp2 others(8): Show |
a0001a0002a0004 | a0001c0001a0001c0006a0002c0002others(1): Show | a0001c0001t0002a0001c0006t0002a0002c0002t0002others(2): Show | a0001c0001t0002g0003a0001c0001t0002g0136a0001c0006t0002g0032others(5): Show | 11 | 330 | 0.0333 | 1 | c.-18 others(10): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ADAM29_chr4_174913358_174983180 | 174958245 | G | GA | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0008a0001c0009others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | a0001c0001t0001g0102a0001c0001t0001g0133a0001c0001t0001g0140others(122): Show | 153 | 330 | 0.4636 | 1 | c.-18 others(22): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | chr4 | TogoVar | ||||||
ADAM29_chr4_174913358_174983180 | 174962511 | C | CA | intron_variant | MODIFIER | HG01070.hp2 HG01928.hp2 HG02071.hp1 others(19): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0006a0001c0016others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0194a0001c0001t0002g0244a0001c0001t0002g0277others(19): Show | 22 | 330 | 0.0667 | 1 | c.-18 others(11): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr4 | TogoVar |