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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ADAM22_chr7_87929251_88207889 | 88053632 | GAA | G | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(24): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0002c0011others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0011others(8): Show | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0018others(24): Show | 27 | 230 | 0.1174 | -2 | c.324 others(21): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88054588 | CTG | C | intron_variant | MODIFIER | HG00738.hp1 HG01071.hp2 HG01074.hp1 others(34): Show |
a0001a0002a0014 | a0001c0001a0002c0002a0014c0017 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(12): Show | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0025others(34): Show | 37 | 230 | 0.1609 | -2 | c.324 others(21): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88057127 | CTT | C | intron_variant | MODIFIER | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(10): Show |
a0001a0003 | a0001c0001a0001c0012a0003c0003 | a0001c0001t0001a0001c0012t0001a0003c0003t0001others(4): Show | a0001c0001t0001g0055a0001c0001t0001g0062a0001c0001t0001g0065others(10): Show | 13 | 230 | 0.0565 | -2 | c.324 others(21): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88061839 | CTT | C | intron_variant | MODIFIER | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(13): Show |
a0001a0002 | a0001c0001a0001c0018a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0113others(13): Show | 16 | 230 | 0.0696 | -2 | c.324 others(21): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88083587 | TTG | T | intron_variant | MODIFIER | HG00423.hp2 HG00597.hp2 HG01169.hp2 others(56): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0019a0002c0002others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(19): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(56): Show | 59 | 230 | 0.2565 | -2 | c.390 others(19): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88089140 | CAG | C | intron_variant | MODIFIER | HG02145.hp2 HG02615.hp2 HG02647.hp2 others(7): Show |
a0001a0003 | a0001c0012a0003c0003 | a0001c0012t0001a0003c0003t0001a0003c0003t0002others(3): Show | a0001c0012t0001g0011a0003c0003t0001g0046a0003c0003t0001g0051others(7): Show | 10 | 230 | 0.0435 | -2 | c.390 others(21): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88113119 | CTT | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
a0001a0002a0004others(8): Show | a0001c0001a0001c0014a0002c0002others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 105 | 230 | 0.4565 | -2 | c.474 others(19): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88113676 | AAT | A | intron_variant | MODIFIER | HG03209.hp1 NA18980.hp2 NA18988.hp1 others(5): Show |
a0004a0005 | a0004c0004a0005c0005 | a0004c0004t0001a0004c0004t0002a0005c0005t0001others(2): Show | a0004c0004t0001g0074a0004c0004t0002g0067a0004c0004t0002g0070others(5): Show | 8 | 230 | 0.0348 | -2 | c.474 others(17): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88117693 | ATT | A | intron_variant | MODIFIER | HG01243.hp2 HG02109.hp1 HG02257.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(3): Show | a0001c0001t0001g0044a0001c0001t0002g0171a0001c0001t0006g0048others(4): Show | 7 | 230 | 0.0304 | -2 | c.607 others(17): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88118641 | ATC | A | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(115): Show |
a0001a0002a0004others(8): Show | a0001c0001a0001c0014a0002c0002others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(34): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 118 | 230 | 0.5130 | -2 | c.607 others(19): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88118655 | CTA | C | intron_variant | MODIFIER | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(23): Show |
a0001 | a0001c0001a0001c0018a0001c0019 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0029a0001c0001t0001g0060a0001c0001t0001g0079others(23): Show | 26 | 230 | 0.1130 | -2 | c.607 others(19): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88123964 | TAA | T | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp2 HG01978.hp1 others(20): Show |
a0003a0009 | a0003c0003a0009c0009 | a0003c0003t0001a0003c0003t0002a0003c0003t0003others(5): Show | a0003c0003t0001g0007a0003c0003t0001g0009a0003c0003t0001g0023others(20): Show | 23 | 230 | 0.1000 | -2 | c.608 others(19): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88131668 | AAT | A | intron_variant | MODIFIER | HG01071.hp2 HG01074.hp1 HG01169.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(4): Show | a0001c0001t0001g0029a0001c0001t0001g0083a0001c0001t0001g0085others(11): Show | 14 | 230 | 0.0609 | -2 | c.992 others(17): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88135277 | CAA | C | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00597.hp2 others(123): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0012a0001c0014others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(123): Show | 126 | 230 | 0.5478 | -2 | c.116 others(19): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 13/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88162097 | TAC | T | intron_variant | MODIFIER | HG00738.hp2 HG02055.hp2 HG02257.hp1 others(13): Show |
a0001 | a0001c0001a0001c0014a0001c0018others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(7): Show | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0150others(13): Show | 16 | 230 | 0.0696 | -2 | c.190 others(19): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88183857 | TAC | T | intron_variant | MODIFIER | HG00735.hp2 HG00741.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0001 | a0001c0001t0002g0164a0002c0002t0001g0196 | 2 | 230 | 0.0087 | -2 | c.266 others(21): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88202151 | ACT | A | 3_prime_UTR_variant | MODIFIER | HG01074.hp2 HG01106.hp2 HG02698.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0008a0002c0002t0008 | a0001c0001t0008g0087a0002c0002t0008g0208a0002c0002t0008g0217 | 3 | 230 | 0.0130 | -2 | c.*56 others(13): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 5663 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||
ADAM23_chr2_206438532_206626127 | 206439618 | AAT | A | upstream_gene_variant | MODIFIER | HG00323.hp1 HG00738.hp1 HG03225.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0002t0001 | a0001c0001t0001g0190a0001c0001t0001g0290a0001c0001t0002g0333others(1): Show | 4 | 358 | 0.0112 | -2 | c.-42 others(13): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3913 | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206439644 | TAG | T | upstream_gene_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG02630.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(1): Show | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0264others(6): Show | 9 | 358 | 0.0251 | -2 | c.-42 others(13): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3887 | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206439997 | CTG | C | upstream_gene_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(43): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(7): Show | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0154others(41): Show | 46 | 358 | 0.1285 | -2 | c.-38 others(13): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3534 | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206441595 | CAA | C | upstream_gene_variant | MODIFIER | HG00280.hp1 HG00738.hp2 HG01074.hp2 others(31): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002a0001c0002t0003others(1): Show | a0001c0001t0001g0005a0001c0001t0001g0168a0001c0001t0001g0180others(31): Show | 34 | 358 | 0.0950 | -2 | c.-22 others(13): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1936 | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206444998 | ACC | A | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(91): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0007others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(17): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(88): Show | 94 | 358 | 0.2626 | -2 | c.215 others(17): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206460105 | CTT | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(75): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0007others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(12): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(72): Show | 78 | 358 | 0.2179 | -2 | c.432 others(21): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206477880 | TAA | T | intron_variant | MODIFIER | HG00323.hp1 HG00544.hp1 HG01123.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0190a0001c0001t0001g0264a0001c0001t0001g0265others(9): Show | 12 | 358 | 0.0335 | -2 | c.433 others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206493703 | CAA | C | intron_variant | MODIFIER | HG02572.hp2 HG03139.hp2 HG03486.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0042 | a0001c0001t0001g0300a0001c0001t0002g0301a0001c0001t0042g0295 | 3 | 358 | 0.0084 | -2 | c.509 others(21): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206522492 | GAA | G | intron_variant | MODIFIER | HG00099.hp1 HG01167.hp1 HG01169.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132others(1): Show | 4 | 358 | 0.0112 | -2 | c.510 others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206526141 | TAC | T | intron_variant | MODIFIER | HG00642.hp1 HG00741.hp1 HG01070.hp2 others(67): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(9): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0015others(65): Show | 70 | 358 | 0.1955 | -2 | c.510 others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206529795 | ATG | A | intron_variant | MODIFIER | HG02257.hp2 HG02258.hp2 HG03471.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006a0001c0001t0001g0170 | 3 | 358 | 0.0084 | -2 | c.510 others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206540216 | TAC | T | intron_variant | MODIFIER | HG00280.hp1 HG00609.hp1 HG00738.hp2 others(68): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(12): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(66): Show | 71 | 358 | 0.1983 | -2 | c.574 others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206544613 | ATT | A | intron_variant | MODIFIER | HG00673.hp2 HG01169.hp2 HG02258.hp1 others(30): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(3): Show | a0001c0001t0001g0271a0001c0001t0001g0308a0001c0001t0001g0309others(30): Show | 33 | 358 | 0.0922 | -2 | c.720 others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206572743 | GTA | G | intron_variant | MODIFIER | HG03486.hp2 HG03540.hp1 HG03579.hp1 others(1): Show |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0014 | a0001c0002t0002g0032a0001c0002t0002g0033a0001c0002t0014g0020others(1): Show | 4 | 358 | 0.0112 | -2 | c.165 others(19): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 17/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206578559 | CAT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0005others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(37): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 288 | 358 | 0.8045 | -2 | c.173 others(21): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206596899 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(50): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0017a0001c0001t0018others(3): Show | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0059others(49): Show | 53 | 358 | 0.1480 | -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 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0088others(83): Show | 88 | 358 | 0.2458 | -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 | a0001c0002t0001g0281a0001c0002t0001g0283a0001c0002t0001g0285others(47): Show | 51 | 348 | 0.1466 | -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 | a0001c0002t0001g0281a0001c0002t0001g0283a0001c0002t0001g0285others(55): Show | 60 | 348 | 0.1724 | -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 |
a0001a0003a0006others(1): Show | a0001c0025a0003c0005a0006c0010others(2): Show | a0001c0025t0042a0003c0005t0005a0003c0005t0006others(3): Show | a0001c0025t0042g0249a0003c0005t0005g0245a0003c0005t0005g0246others(9): Show | 12 | 348 | 0.0345 | -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 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | 348 | 0.0115 | -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 | a0001c0001t0002g0228a0001c0001t0044g0227a0001c0002t0001g0027others(81): Show | 91 | 348 | 0.2615 | -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 | a0001c0001t0001g0005a0001c0001t0001g0030 | 3 | 348 | 0.0086 | -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 | a0001c0001t0001g0043a0001c0001t0002g0047a0001c0001t0017g0028 | 3 | 348 | 0.0086 | -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 | a0001c0001t0003g0207a0002c0007t0002g0124a0002c0007t0026g0102 | 3 | 348 | 0.0086 | -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 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(1): Show | 4 | 348 | 0.0115 | -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 |
a0005a0019 | a0005c0008a0019c0032 | a0005c0008t0002a0019c0032t0033 | a0005c0008t0002g0325a0005c0008t0002g0326a0005c0008t0002g0327others(2): Show | 5 | 348 | 0.0144 | -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 |
a0002a0005a0006others(1): Show | a0002c0003a0002c0007a0002c0019others(7): Show | a0002c0003t0001a0002c0003t0002a0002c0003t0003others(18): Show | a0002c0003t0001g0001a0002c0003t0001g0250a0002c0003t0001g0255others(36): Show | 44 | 348 | 0.1264 | -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 | a0001c0001t0004g0051a0001c0001t0004g0071a0001c0001t0004g0082others(27): Show | 30 | 348 | 0.0862 | -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(334): Show |
a0001a0002a0003others(15): Show | a0001c0001a0001c0002a0001c0013others(28): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(82): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(316): Show | 337 | 348 | 0.9684 | -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(336): Show |
a0001a0002a0003others(16): Show | a0001c0001a0001c0002a0001c0013others(29): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(84): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(318): Show | 339 | 348 | 0.9741 | -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 | a0001c0001t0003g0010a0001c0001t0003g0046a0002c0002t0001g0017others(5): Show | 9 | 330 | 0.0273 | -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 |
a0001a0002a0007 | a0001c0006a0002c0002a0007c0012 | a0001c0006t0002a0002c0002t0002a0007c0012t0014 | a0001c0006t0002g0032a0001c0006t0002g0033a0002c0002t0002g0029others(2): Show | 5 | 330 | 0.0152 | -2 | c.-26 others(13): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 1981 | chr4 | TogoVar |