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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SNX10_chr7_26286862_26379383 | 26358805 | G | GTTTTTTT others(4): Show |
intron_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0077 | 1 | 192 | 0.0052 | 11 | c.25- others(26): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX11_chr17_48102766_48128601 | 48105324 | C | CTTTTTTT others(4): Show |
upstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(1): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(48): Show |
81 | 130 | 0.6231 | 11 | c.-25 others(22): Show |
SNX11 | ENSG00000002919.15 | transcript | ENST00000359238.7 | protein_coding | 2441 | chr17 | TogoVar | |||||||
SNX12_chrX_71054247_71073334 | 71071560 | A | ATATATAT others(4): Show |
upstream_gene_variant | MODIFIER | HG02970.hp1 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0017 | 1 | 304 | 0.0033 | 11 | c.-32 others(22): Show |
SNX12 | ENSG00000147164.12 | transcript | ENST00000374274.8 | protein_coding | 3227 | chrX | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17944640 | T | TTTATAAT others(4): Show |
upstream_gene_variant | MODIFIER | HG00323.hp2 HG00408.hp2 HG02056.hp1 others(21): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0002t0002others(4): Show | a0001c0001t0001g0021 a0001c0001t0001g0245 a0001c0001t0003g0244 others(21): Show |
24 | 336 | 0.0714 | 11 | c.-43 others(22): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 4147 | chr7 | TogoVar | |||||||
SNX15_chr11_65022439_65045572 | 65025779 | C | CTTTTTTT others(4): Show |
upstream_gene_variant | MODIFIER | HG01928.hp2 HG01952.hp1 HG02055.hp2 others(11): Show |
a0001a0002 | a0001c0002a0001c0006a0002c0003 | a0001c0002t0002a0001c0006t0004a0002c0003t0003others(1): Show | a0001c0002t0002g0106 a0001c0002t0002g0108 a0001c0002t0002g0109 others(9): Show |
14 | 159 | 0.0881 | 11 | c.-17 others(22): Show |
SNX15 | ENSG00000110025.13 | transcript | ENST00000377244.8 | protein_coding | 1659 | chr11 | TogoVar | |||||||
SNX15_chr11_65022439_65045572 | 65039029 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02300.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0049 | 1 | 157 | 0.0064 | 11 | c.922 others(26): Show |
SNX15 | ENSG00000110025.13 | transcript | ENST00000377244.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
SNX16_chr8_81794583_81847185 | 81842348 | G | GAGAGAGG others(4): Show |
upstream_gene_variant | MODIFIER | HG01074.hp2 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0012 | 1 | 297 | 0.0034 | 11 | c.-32 others(20): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 164 | chr8 | TogoVar | |||||||
SNX16_chr8_81794583_81847185 | 81842382 | G | GGGAGGGA others(4): Show |
upstream_gene_variant | MODIFIER | HG01169.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0017 | 1 | 303 | 0.0033 | 11 | c.-35 others(20): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 198 | chr8 | TogoVar | |||||||
SNX16_chr8_81794583_81847185 | 81842383 | G | GAGAGAGA others(4): Show |
upstream_gene_variant | MODIFIER | HG02970.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0048 | 1 | 210 | 0.0048 | 11 | c.-35 others(20): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 199 | chr8 | TogoVar | |||||||
SNX18_chr5_54512759_54551586 | 54512874 | C | CCTTCCTT others(4): Show |
upstream_gene_variant | MODIFIER | HG02559.hp2 NA18972.hp1 NA18986.hp1 |
a0001 | a0001c0001a0001c0011 | a0001c0001t0002a0001c0001t0027a0001c0011t0009 | a0001c0001t0002g0094 a0001c0001t0027g0095 a0001c0011t0009g0051 |
3 | 306 | 0.0098 | 11 | c.-50 others(22): Show |
SNX18 | ENSG00000178996.14 | transcript | ENST00000381410.5 | protein_coding | 4884 | chr5 | TogoVar | |||||||
SNX18_chr5_54512759_54551586 | 54513672 | A | ATTATATA others(4): Show |
upstream_gene_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(32): Show |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0002a0001c0003t0004others(7): Show | a0001c0003t0001g0108 a0001c0003t0002g0111 a0001c0003t0004g0114 others(21): Show |
35 | 384 | 0.0911 | 11 | c.-42 others(22): Show |
SNX18 | ENSG00000178996.14 | transcript | ENST00000381410.5 | protein_coding | 4086 | chr5 | TogoVar | |||||||
SNX18_chr5_54512759_54551586 | 54530744 | A | ATTTTTTT others(4): Show |
intron_variant | MODIFIER | HG00609.hp2 HG00733.hp2 HG00741.hp1 others(52): Show |
a0001a0005 | a0001c0002a0001c0004a0001c0006others(1): Show | a0001c0002t0001a0001c0002t0008a0001c0002t0016others(11): Show | a0001c0002t0001g0004 a0001c0002t0001g0047 a0001c0002t0001g0138 others(29): Show |
55 | 60 | 0.9167 | 11 | c.162 others(32): Show |
SNX18 | ENSG00000178996.14 | transcript | ENST00000381410.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
SNX19_chr11_130861250_130921479 | 130865946 | T | TGACAGGG others(4): Show |
downstream_gene_variant | MODIFIER | HG00741.hp2 HG01070.hp2 HG02717.hp2 others(3): Show |
a0004 | a0004c0009 | a0004c0009t0009 | a0004c0009t0009g0044 a0004c0009t0009g0284 a0004c0009t0009g0285 others(2): Show |
6 | 412 | 0.0146 | 11 | c.*12 others(24): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 303 | chr11 | TogoVar | |||||||
SNX22_chr15_64146731_64162481 | 64160924 | A | ACAGGTGT others(4): Show |
downstream_gene_variant | MODIFIER | HG03710.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0005 | 1 | 348 | 0.0029 | 11 | c.*64 others(22): Show |
SNX22 | ENSG00000157734.14 | transcript | ENST00000325881.9 | protein_coding | 3444 | chr15 | TogoVar | |||||||
SNX25_chr4_185204598_185368966 | 185212491 | G | GTGTGTTT others(4): Show |
intron_variant | MODIFIER | HG01123.hp1 HG01123.hp2 HG01928.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(4): Show |
7 | 79 | 0.0886 | 11 | c.429 others(28): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185212491 | G | GTGTTTCT others(4): Show |
intron_variant | MODIFIER | HG00733.hp2 HG01891.hp2 HG02257.hp2 others(17): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0007others(1): Show | a0001c0001t0001a0002c0002t0001a0002c0002t0004others(2): Show | a0001c0001t0001g0185 a0002c0002t0001g0251 a0002c0002t0001g0252 others(17): Show |
20 | 92 | 0.2174 | 11 | c.429 others(28): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185212491 | G | GTGTTTTT others(4): Show |
intron_variant | MODIFIER | HG00621.hp1 HG00639.hp2 HG00741.hp2 others(67): Show |
a0001a0005a0006others(2): Show | a0001c0001a0001c0003a0005c0008others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(4): Show | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(67): Show |
70 | 142 | 0.4930 | 11 | c.429 others(28): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX27_chr1_151607050_151704080 | 151667247 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(78): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(45): Show | a0001c0001t0001g0229 a0001c0001t0001g0235 a0001c0001t0001g0246 others(77): Show |
81 | 92 | 0.8804 | 11 | c.986 others(28): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SNX27_chr1_151607050_151704080 | 151681235 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008a0001c0001t0037 | a0001c0001t0001g0232 a0001c0001t0008g0193 a0001c0001t0037g0192 others(1): Show |
4 | 122 | 0.0328 | 11 | c.115 others(30): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 11975141 | C | CTTTTCTT others(4): Show |
upstream_gene_variant | MODIFIER | HG02257.hp2 HG03490.hp1 HG03688.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0013 | a0001c0001t0032a0001c0001t0059a0001c0002t0005others(1): Show | a0001c0001t0032g0130 a0001c0001t0059g0173 a0001c0002t0005g0168 others(1): Show |
4 | 15 | 0.2667 | 11 | c.-16 others(22): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 1592 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12013488 | G | GAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02683.hp1 | a0001 | a0001c0002 | a0001c0002t0064 | a0001c0002t0064g0107 | 1 | 146 | 0.0068 | 11 | c.122 others(30): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12013500 | A | AAAAATAT others(4): Show |
intron_variant | MODIFIER | HG01993.hp2 | a0001 | a0001c0001 | a0001c0001t0039 | a0001c0001t0039g0047 | 1 | 54 | 0.0185 | 11 | c.122 others(30): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12013500 | A | AAATATAT others(4): Show |
intron_variant | MODIFIER | HG01069.hp2 | a0001 | a0001c0004 | a0001c0004t0095 | a0001c0004t0095g0146 | 1 | 54 | 0.0185 | 11 | c.122 others(30): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12013500 | A | ATATATAT others(4): Show |
intron_variant | MODIFIER | HG03486.hp1 | a0001 | a0001c0002 | a0001c0002t0084 | a0001c0002t0084g0066 | 1 | 54 | 0.0185 | 11 | c.122 others(30): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 3/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12063366 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG03491.hp1 | a0008 | a0008c0010 | a0008c0010t0098 | a0008c0010t0098g0022 | 1 | 18 | 0.0556 | 11 | c.124 others(30): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12118313 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG00558.hp1 HG02015.hp2 HG03704.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0012a0001c0001t0014a0001c0001t0045others(6): Show | a0001c0001t0012g0095 a0001c0001t0014g0118 a0001c0001t0045g0155 others(7): Show |
10 | 65 | 0.1538 | 11 | c.140 others(30): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12242564 | C | CTCTTTTC others(4): Show |
intron_variant | MODIFIER | HG02615.hp2 HG02622.hp1 HG03225.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0001t0006a0001c0001t0013others(2): Show | a0001c0001t0002g0169 a0001c0001t0006g0064 a0001c0001t0013g0009 others(2): Show |
5 | 169 | 0.0296 | 11 | c.167 others(32): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12242579 | T | TTTCTTCT others(4): Show |
intron_variant | MODIFIER | HG01081.hp1 HG02258.hp2 HG02976.hp1 others(2): Show |
a0001 | a0001c0003a0001c0006a0001c0007 | a0001c0003t0058a0001c0006t0011a0001c0006t0066others(2): Show | a0001c0003t0058g0094 a0001c0006t0011g0041 a0001c0006t0066g0004 others(2): Show |
5 | 172 | 0.0291 | 11 | c.167 others(32): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12334901 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02615.hp2 NA18906.hp1 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0024a0001c0003t0016 | a0001c0002t0024g0128 a0001c0003t0016g0029 |
2 | 7 | 0.2857 | 11 | c.178 others(32): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12339370 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02451.hp2 HG02630.hp2 HG02886.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0017a0001c0001t0027a0001c0001t0034others(4): Show | a0001c0001t0017g0103 a0001c0001t0027g0083 a0001c0001t0034g0030 others(4): Show |
7 | 44 | 0.1591 | 11 | c.178 others(32): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12380784 | C | CCCACCAT others(4): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(52): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(43): Show | a0001c0001t0001g0113 a0001c0001t0001g0163 a0001c0001t0002g0020 others(52): Show |
55 | 171 | 0.3216 | 11 | c.190 others(32): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12380784 | C | CCCATCAT others(4): Show |
intron_variant | MODIFIER | HG01261.hp2 HG02257.hp2 HG03486.hp2 |
a0001 | a0001c0001a0001c0002a0001c0013 | a0001c0001t0002a0001c0002t0024a0001c0013t0092 | a0001c0001t0002g0169 a0001c0002t0024g0050 a0001c0013t0092g0126 |
3 | 119 | 0.0252 | 11 | c.190 others(32): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12381083 | C | CCCACCCA others(4): Show |
intron_variant | MODIFIER | HG02683.hp1 HG03834.hp1 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0064a0001c0003t0051 | a0001c0002t0064g0107 a0001c0003t0051g0131 |
2 | 172 | 0.0116 | 11 | c.190 others(32): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12408157 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG01074.hp2 | a0001 | a0001c0004 | a0001c0004t0081 | a0001c0004t0081g0068 | 1 | 92 | 0.0109 | 11 | c.203 others(30): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12408181 | A | AAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0004 | a0001c0004t0090 | a0001c0004t0090g0102 | 1 | 90 | 0.0111 | 11 | c.203 others(30): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12431434 | C | CTTCTTCT others(4): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0001 | a0001c0001t0034 | a0001c0001t0034g0030 | 1 | 133 | 0.0075 | 11 | c.203 others(32): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12461978 | A | AAAAAAAA others(4): Show |
intron_variant | MODIFIER | NA19070.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0175 | 1 | 86 | 0.0116 | 11 | c.203 others(32): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12461978 | A | AATAATAT others(4): Show |
intron_variant | MODIFIER | NA18942.hp2 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0137 | 1 | 86 | 0.0116 | 11 | c.203 others(32): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12476383 | A | AAAAATAT others(4): Show |
intron_variant | MODIFIER | HG00673.hp1 | a0001 | a0001c0001 | a0001c0001t0048 | a0001c0001t0048g0140 | 1 | 117 | 0.0085 | 11 | c.203 others(30): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12483114 | G | GTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0169 | 1 | 54 | 0.0185 | 11 | c.217 others(30): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12549530 | C | CATATAGC others(4): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(134): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0003others(17): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(108): Show | a0001c0001t0001g0127 a0001c0001t0002g0020 a0001c0001t0002g0065 others(134): Show |
137 | 168 | 0.8155 | 11 | c.231 others(32): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12549530 | C | CATGTAGC others(4): Show |
intron_variant | MODIFIER | HG02015.hp2 NA18986.hp1 |
a0001 | a0001c0004 | a0001c0004t0003a0001c0004t0005 | a0001c0004t0003g0161 a0001c0004t0005g0171 |
2 | 33 | 0.0606 | 11 | c.231 others(32): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12557015 | A | ACACCCCC others(4): Show |
intron_variant | MODIFIER | HG01069.hp1 HG02257.hp2 |
a0001 | a0001c0003a0001c0013 | a0001c0003t0004a0001c0013t0092 | a0001c0003t0004g0093 a0001c0013t0092g0126 |
2 | 89 | 0.0225 | 11 | c.231 others(32): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12562971 | T | TAGCAAAG others(4): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(64): Show |
a0001a0003a0005others(1): Show | a0001c0001a0001c0002a0001c0004others(8): Show | a0001c0001t0028a0001c0002t0003a0001c0002t0005others(52): Show | a0001c0001t0028g0123 a0001c0002t0003g0051 a0001c0002t0003g0136 others(64): Show |
67 | 174 | 0.3851 | 11 | c.231 others(30): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 20/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12568303 | T | TAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02040.hp2 NA18990.hp1 NA19070.hp2 |
a0001 | a0001c0002 | a0001c0002t0003a0001c0002t0073a0001c0002t0088 | a0001c0002t0003g0152 a0001c0002t0073g0129 a0001c0002t0088g0170 |
3 | 109 | 0.0275 | 11 | c.231 others(28): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 20/20 | chr16 | TogoVar | |||||||
SNX30_chr9_112745760_112879987 | 112791399 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | NA18963.hp2 NA18998.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0287 a0001c0001t0003g0277 |
2 | 37 | 0.0541 | 11 | c.157 others(30): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112817401 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00642.hp2 HG01192.hp1 others(18): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0264 a0001c0001t0002g0058 a0001c0001t0002g0059 others(18): Show |
21 | 28 | 0.7500 | 11 | c.349 others(26): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112834882 | A | ACACACAC others(4): Show |
intron_variant | MODIFIER | NA18978.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0114 | 1 | 133 | 0.0075 | 11 | c.619 others(28): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX31_chr8_100567889_100654665 | 100573703 | G | GCTGTGGT others(4): Show |
3_prime_UTR_variant | MODIFIER | HG00642.hp1 HG01168.hp1 |
a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0053 a0001c0001t0008g0098 |
2 | 302 | 0.0066 | 11 | c.*15 others(20): Show |
SNX31 | ENSG00000174226.9 | transcript | ENST00000311812.7 | protein_coding | 14/14 | 161 | chr8 | TogoVar | ||||||
SNX31_chr8_100567889_100654665 | 100634756 | T | TAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG03927.hp1 | a0005 | a0005c0005 | a0005c0005t0004 | a0005c0005t0004g0152 | 1 | 231 | 0.0043 | 11 | c.256 others(28): Show |
SNX31 | ENSG00000174226.9 | transcript | ENST00000311812.7 | protein_coding | 3/13 | chr8 | TogoVar |