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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SNX25_chr4_185204598_185368966 | 185250722 | GT | G | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(80): Show |
a0001a0005a0011others(1): Show | a0001c0001a0001c0003a0001c0009others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(80): Show |
83 | 276 | 0.3007 | -1 | c.514 others(9): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185254850 | GA | G | intron_variant | MODIFIER | HG01123.hp1 HG01168.hp2 HG01192.hp1 others(45): Show |
a0001a0003a0013 | a0001c0001a0001c0003a0003c0004others(1): Show | a0001c0001t0001a0001c0003t0001a0003c0004t0001others(1): Show | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0078 others(44): Show |
48 | 276 | 0.1739 | -1 | c.515 others(9): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185256624 | CT | C | intron_variant | MODIFIER | HG00639.hp1 HG02165.hp2 HG02293.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0133 a0001c0001t0001g0167 a0001c0001t0001g0171 others(2): Show |
5 | 276 | 0.0181 | -1 | c.515 others(9): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185257176 | GA | G | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(93): Show |
a0001a0002a0007others(2): Show | a0001c0001a0001c0003a0001c0009others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(93): Show |
96 | 276 | 0.3478 | -1 | c.515 others(9): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185260414 | CT | C | intron_variant | MODIFIER | HG01081.hp2 HG01243.hp1 HG01361.hp2 others(11): Show |
a0001a0005a0008 | a0001c0001a0005c0008a0008c0017 | a0001c0001t0001a0005c0008t0001a0008c0017t0001 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0016 others(11): Show |
14 | 276 | 0.0507 | -1 | c.731 others(9): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185265005 | TC | T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(93): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0009others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): Show |
96 | 276 | 0.3478 | -1 | c.904 others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 4/18 | chr4 | TogoVar | |||||||
SNX25_chr4_185204598_185368966 | 185267219 | TA | T | intron_variant | MODIFIER | HG01167.hp2 HG02965.hp2 HG03139.hp1 others(4): Show |
a0001a0006 | a0001c0001a0001c0003a0006c0019 | a0001c0001t0001a0001c0003t0001a0006c0019t0005 | a0001c0001t0001g0023 a0001c0001t0001g0039 a0001c0001t0001g0113 others(4): Show |
7 | 276 | 0.0254 | -1 | c.109 others(8): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185267729 | TA | T | intron_variant | MODIFIER | HG02145.hp1 HG02257.hp2 HG02615.hp2 others(6): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0003t0001a0002c0002t0001 | a0001c0001t0001g0167 a0001c0001t0001g0220 a0001c0001t0001g0221 others(6): Show |
9 | 276 | 0.0326 | -1 | c.109 others(9): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185270079 | CA | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(115): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0003a0001c0006others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
118 | 276 | 0.4275 | -1 | c.109 others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185277720 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00621.hp1 HG01106.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020 a0001c0001t0001g0037 a0001c0001t0001g0041 others(4): Show |
7 | 276 | 0.0254 | -1 | c.109 others(11): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185291166 | GA | G | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(121): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0003a0001c0006others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
124 | 276 | 0.4493 | -1 | c.116 others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185292281 | TA | T | intron_variant | MODIFIER | HG02630.hp2 HG03486.hp2 NA18522.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(1): Show |
4 | 276 | 0.0145 | -1 | c.116 others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185295451 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(107): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0003a0001c0006others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(107): Show |
110 | 276 | 0.3986 | -1 | c.116 others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185300163 | AT | A | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(114): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0003a0001c0006others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(114): Show |
117 | 276 | 0.4239 | -1 | c.116 others(11): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185314856 | CA | C | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(99): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0003a0001c0006others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(99): Show |
102 | 276 | 0.3696 | -1 | c.134 others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185315236 | AG | A | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00639.hp2 others(78): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0003a0001c0014others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(78): Show |
81 | 276 | 0.2935 | -1 | c.134 others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | TogoVar | |||||||
SNX25_chr4_185204598_185368966 | 185315292 | AT | A | intron_variant | MODIFIER | HG00639.hp1 HG00733.hp1 HG00733.hp2 others(70): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(4): Show | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0049 others(69): Show |
73 | 276 | 0.2645 | -1 | c.134 others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185319090 | TA | T | intron_variant | MODIFIER | HG00733.hp1 HG01074.hp2 HG01081.hp2 others(48): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0006a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0006t0001others(5): Show | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0021 others(48): Show |
51 | 276 | 0.1848 | -1 | c.134 others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | chr4 | TogoVar | |||||||
SNX25_chr4_185204598_185368966 | 185319091 | AT | A | intron_variant | MODIFIER | HG00544.hp2 HG01168.hp2 HG02280.hp2 others(18): Show |
a0001a0003a0008others(1): Show | a0001c0001a0001c0003a0003c0004others(2): Show | a0001c0001t0001a0001c0003t0001a0003c0004t0001others(2): Show | a0001c0001t0001g0213 a0001c0001t0001g0238 a0001c0003t0001g0067 others(18): Show |
21 | 276 | 0.0761 | -1 | c.134 others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185319193 | CT | C | intron_variant | MODIFIER | HG00733.hp1 HG00733.hp2 HG01074.hp2 others(81): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0004others(3): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(5): Show | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(80): Show |
84 | 276 | 0.3044 | -1 | c.134 others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185321262 | AT | A | intron_variant | MODIFIER | HG02896.hp2 HG03225.hp1 NA18941.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0001 | a0001c0001t0001g0113 a0001c0001t0001g0178 a0001c0001t0002g0145 others(2): Show |
5 | 276 | 0.0181 | -1 | c.147 others(9): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185334036 | CA | C | intron_variant | MODIFIER | HG01496.hp1 HG01928.hp2 HG01952.hp1 others(13): Show |
a0001a0007a0010 | a0001c0001a0007c0018a0010c0015 | a0001c0001t0001a0001c0001t0002a0007c0018t0001others(1): Show | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0033 others(13): Show |
16 | 276 | 0.0580 | -1 | c.191 others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185338277 | TG | T | intron_variant | MODIFIER | HG01081.hp1 HG02055.hp1 HG02257.hp1 others(13): Show |
a0001a0002a0014 | a0001c0001a0002c0002a0014c0010 | a0001c0001t0001a0002c0002t0001a0014c0010t0001 | a0001c0001t0001g0153 a0001c0001t0001g0191 a0001c0001t0001g0192 others(13): Show |
16 | 276 | 0.0580 | -1 | c.191 others(10): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 10/18 | chr4 | TogoVar | |||||||
SNX25_chr4_185204598_185368966 | 185345789 | CA | C | intron_variant | MODIFIER | HG01081.hp2 HG01361.hp2 HG01433.hp1 others(16): Show |
a0001a0003a0005others(2): Show | a0001c0001a0001c0006a0003c0007others(3): Show | a0001c0001t0001a0001c0006t0001a0003c0007t0001others(3): Show | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0021 others(16): Show |
19 | 276 | 0.0688 | -1 | c.218 others(9): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185352981 | TG | T | intron_variant | MODIFIER | HG00621.hp2 HG00733.hp2 HG02145.hp1 others(27): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0006a0002c0002others(3): Show | a0001c0001t0001a0001c0006t0001a0002c0002t0001others(3): Show | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(27): Show |
30 | 276 | 0.1087 | -1 | c.246 others(9): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185354041 | CA | C | intron_variant | MODIFIER | HG00621.hp1 HG00639.hp1 HG01106.hp1 others(66): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0003t0001others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(64): Show |
69 | 276 | 0.2500 | -1 | c.258 others(9): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185362837 | CT | C | intron_variant | MODIFIER | HG00140.hp2 HG00621.hp1 HG00733.hp1 others(75): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(73): Show |
78 | 276 | 0.2826 | -1 | c.293 others(9): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185365692 | AT | A | downstream_gene_variant | MODIFIER | HG00140.hp2 HG00621.hp1 HG00733.hp1 others(61): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0019 | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(60): Show |
64 | 276 | 0.2319 | -1 | c.*22 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1727 | chr4 | TogoVar | |||||||
SNX25_chr4_185204598_185368966 | 185367303 | CT | C | downstream_gene_variant | MODIFIER | HG00621.hp1 HG00621.hp2 HG01123.hp1 others(68): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0004others(1): Show | a0001c0001t0001a0001c0001t0003a0002c0002t0001others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(66): Show |
71 | 276 | 0.2573 | -1 | c.*38 others(6): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3338 | chr4 | TogoVar | |||||||
SNX27_chr1_151607050_151704080 | 151607942 | AT | A | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(51): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(29): Show | a0001c0001t0003g0006 a0001c0001t0004g0156 a0001c0001t0004g0158 others(51): Show |
54 | 366 | 0.1475 | -1 | c.-42 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 4107 | chr1 | TogoVar | |||||||
SNX27_chr1_151607050_151704080 | 151610264 | CT | C | upstream_gene_variant | MODIFIER | HG02717.hp2 HG02895.hp1 HG03579.hp1 others(3): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0009a0001c0001t0015a0001c0001t0022others(2): Show | a0001c0001t0009g0232 a0001c0001t0015g0296 a0001c0001t0022g0320 others(3): Show |
6 | 366 | 0.0164 | -1 | c.-19 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1785 | chr1 | TogoVar | |||||||
SNX27_chr1_151607050_151704080 | 151611042 | TA | T | upstream_gene_variant | MODIFIER | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(12): Show |
a0001a0003 | a0001c0001a0001c0004a0003c0005 | a0001c0001t0019a0001c0001t0024a0001c0001t0039others(7): Show | a0001c0001t0019g0277 a0001c0001t0019g0278 a0001c0001t0019g0279 others(11): Show |
15 | 366 | 0.0410 | -1 | c.-11 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1007 | chr1 | TogoVar | |||||||
SNX27_chr1_151607050_151704080 | 151611056 | AC | A | upstream_gene_variant | MODIFIER | HG01167.hp2 HG02015.hp1 HG03239.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0050a0001c0001t0085others(1): Show | a0001c0001t0005g0147 a0001c0001t0050g0234 a0001c0001t0085g0346 others(1): Show |
4 | 366 | 0.0109 | -1 | c.-11 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 993 | chr1 | TogoVar | |||||||
SNX27_chr1_151607050_151704080 | 151611770 | AG | A | upstream_gene_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(51): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0008a0001c0001t0020others(27): Show | a0001c0001t0002g0030 a0001c0001t0002g0033 a0001c0001t0002g0036 others(51): Show |
54 | 366 | 0.1475 | -1 | c.-43 others(5): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 279 | chr1 | TogoVar | |||||||
SNX27_chr1_151607050_151704080 | 151617878 | GT | G | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(30): Show |
a0001a0003 | a0001c0001a0003c0005 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(21): Show | a0001c0001t0003g0100 a0001c0001t0004g0156 a0001c0001t0004g0158 others(30): Show |
33 | 366 | 0.0902 | -1 | c.311 others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SNX27_chr1_151607050_151704080 | 151618473 | CT | C | intron_variant | MODIFIER | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0024a0001c0001t0069a0001c0001t0070 | a0001c0001t0024g0354 a0001c0001t0024g0355 a0001c0001t0024g0356 others(2): Show |
5 | 366 | 0.0137 | -1 | c.311 others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
SNX27_chr1_151607050_151704080 | 151619011 | CA | C | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(108): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002 | a0001c0001t0003a0001c0001t0006a0001c0001t0007others(52): Show | a0001c0001t0003g0099 a0001c0001t0006g0001 a0001c0001t0006g0188 others(105): Show |
111 | 366 | 0.3033 | -1 | c.311 others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SNX27_chr1_151607050_151704080 | 151624434 | TA | T | intron_variant | MODIFIER | HG02723.hp2 HG02738.hp1 NA19066.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0028a0001c0001t0067 | a0001c0001t0003g0100 a0001c0001t0028g0170 a0001c0001t0067g0361 |
3 | 366 | 0.0082 | -1 | c.311 others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
SNX27_chr1_151607050_151704080 | 151626265 | CT | C | intron_variant | MODIFIER | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(18): Show |
a0001 | a0001c0001 | a0001c0001t0011a0001c0001t0013a0001c0001t0019others(8): Show | a0001c0001t0011g0243 a0001c0001t0011g0262 a0001c0001t0011g0264 others(18): Show |
21 | 366 | 0.0574 | -1 | c.312 others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SNX27_chr1_151607050_151704080 | 151626277 | TG | T | intron_variant | MODIFIER | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0012a0001c0001t0054a0001c0001t0080others(1): Show | a0001c0001t0012g0102 a0001c0001t0012g0104 a0001c0001t0012g0106 others(5): Show |
8 | 366 | 0.0219 | -1 | c.312 others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
SNX27_chr1_151607050_151704080 | 151628006 | GT | G | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(104): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(52): Show | a0001c0001t0002g0036 a0001c0001t0004g0317 a0001c0001t0006g0001 others(101): Show |
107 | 366 | 0.2924 | -1 | c.312 others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SNX27_chr1_151607050_151704080 | 151629083 | CT | C | intron_variant | MODIFIER | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0012a0001c0001t0054a0001c0001t0080others(1): Show | a0001c0001t0012g0102 a0001c0001t0012g0104 a0001c0001t0012g0106 others(6): Show |
9 | 366 | 0.0246 | -1 | c.312 others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SNX27_chr1_151607050_151704080 | 151633644 | CA | C | intron_variant | MODIFIER | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0011a0001c0001t0019a0001c0001t0060others(7): Show | a0001c0001t0011g0243 a0001c0001t0011g0262 a0001c0001t0011g0264 others(14): Show |
17 | 366 | 0.0465 | -1 | c.312 others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SNX27_chr1_151607050_151704080 | 151636666 | TA | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
a0001a0002a0003 | a0001c0001a0001c0007a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(102): Show | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0119 others(223): Show |
229 | 366 | 0.6257 | -1 | c.312 others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SNX27_chr1_151607050_151704080 | 151637149 | TC | T | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(77): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0006a0001c0001t0007a0001c0001t0009others(34): Show | a0001c0001t0006g0001 a0001c0001t0006g0188 a0001c0001t0006g0189 others(75): Show |
80 | 366 | 0.2186 | -1 | c.312 others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
SNX27_chr1_151607050_151704080 | 151637161 | TG | T | intron_variant | MODIFIER | HG00280.hp1 HG00423.hp2 HG00735.hp2 others(46): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(26): Show | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(46): Show |
49 | 366 | 0.1339 | -1 | c.312 others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
SNX27_chr1_151607050_151704080 | 151637169 | TG | T | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(118): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0006a0001c0001t0007a0001c0001t0009others(61): Show | a0001c0001t0006g0001 a0001c0001t0006g0189 a0001c0001t0007g0214 others(115): Show |
121 | 366 | 0.3306 | -1 | c.312 others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
SNX27_chr1_151607050_151704080 | 151648744 | TA | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
a0001a0003 | a0001c0001a0001c0006a0001c0007others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(59): Show | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0118 others(144): Show |
148 | 366 | 0.4044 | -1 | c.544 others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | TogoVar | |||||||
SNX27_chr1_151607050_151704080 | 151652927 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0004others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(112): Show | a0001c0001t0001g0113 a0001c0001t0001g0117 a0001c0001t0001g0118 others(240): Show |
247 | 366 | 0.6749 | -1 | c.544 others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SNX27_chr1_151607050_151704080 | 151653934 | GT | G | intron_variant | MODIFIER | HG02895.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0035a0001c0001t0150a0001c0001t0151others(1): Show | a0001c0001t0035g0020 a0001c0001t0035g0021 a0001c0001t0035g0022 others(3): Show |
6 | 366 | 0.0164 | -1 | c.544 others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | TogoVar |