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 | 26325306 | A | AATATATA others(11): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00558.hp2 HG00621.hp2 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0007 a0001c0001t0001g0104 a0001c0001t0001g0149 others(14): Show |
17 | 390 | 0.0436 | 18 | c.-23 others(37): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26358805 | G | GTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG00438.hp2 HG01071.hp1 HG02572.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0365 a0001c0001t0001g0367 a0001c0001t0004g0117 others(3): Show |
6 | 390 | 0.0154 | 18 | c.25- others(33): 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(11): Show |
upstream_gene_variant | MODIFIER | HG01069.hp2 HG03209.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0016 | 2 | 416 | 0.0048 | 18 | c.-25 others(29): Show |
SNX11 | ENSG00000002919.15 | transcript | ENST00000359238.7 | protein_coding | 2441 | chr17 | TogoVar | |||||||
SNX12_chrX_71054247_71073334 | 71070675 | A | ATACACTA others(11): Show |
upstream_gene_variant | MODIFIER | NA18967.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0032 | 1 | 309 | 0.0032 | 18 | c.-23 others(29): Show |
SNX12 | ENSG00000147164.12 | transcript | ENST00000374274.8 | protein_coding | 2342 | chrX | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17801009 | C | CATATATA others(11): Show |
intron_variant | MODIFIER | NA19004.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0200 | 1 | 338 | 0.0030 | 18 | c.229 others(35): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17801018 | A | ATATATAT others(11): Show |
intron_variant | MODIFIER | HG02970.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0192 | 1 | 338 | 0.0030 | 18 | c.229 others(35): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17805211 | T | TTGTGTGT others(11): Show |
intron_variant | MODIFIER | HG01074.hp1 HG02280.hp2 HG03486.hp2 |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0001t0008a0001c0007t0025 | a0001c0001t0001g0229 a0001c0001t0008g0004 a0001c0007t0025g0003 |
3 | 338 | 0.0089 | 18 | c.206 others(37): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17805250 | T | TGTGCGTG others(11): Show |
intron_variant | MODIFIER | HG00741.hp2 HG02273.hp2 NA18945.hp2 |
a0001 | a0001c0002 | a0001c0002t0006a0001c0002t0009 | a0001c0002t0006g0266 a0001c0002t0009g0263 a0001c0002t0009g0331 |
3 | 338 | 0.0089 | 18 | c.206 others(37): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17805250 | T | TGTGTGTG others(11): Show |
intron_variant | MODIFIER | HG00639.hp1 | a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0145 | 1 | 338 | 0.0030 | 18 | c.206 others(37): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17841553 | T | TACACACA others(11): Show |
intron_variant | MODIFIER | HG03491.hp1 HG03492.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0026 a0001c0001t0001g0027 |
2 | 338 | 0.0059 | 18 | c.116 others(37): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 12/25 | chr7 | TogoVar | |||||||
SNX15_chr11_65022439_65045572 | 65025779 | C | CTTTTTTT others(11): Show |
upstream_gene_variant | MODIFIER | HG00642.hp2 HG01884.hp1 HG02486.hp1 others(3): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0007others(1): Show | a0001c0001t0004a0001c0002t0004a0002c0007t0007others(1): Show | a0001c0001t0004g0028 a0001c0001t0004g0128 a0001c0002t0004g0145 others(3): Show |
6 | 338 | 0.0178 | 18 | c.-17 others(29): Show |
SNX15 | ENSG00000110025.13 | transcript | ENST00000377244.8 | protein_coding | 1659 | chr11 | TogoVar | |||||||
SNX15_chr11_65022439_65045572 | 65039029 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG03041.hp2 HG03209.hp2 NA18906.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0002t0004 | a0001c0001t0004g0028 a0001c0001t0004g0065 a0001c0002t0004g0028 |
4 | 338 | 0.0118 | 18 | c.922 others(33): Show |
SNX15 | ENSG00000110025.13 | transcript | ENST00000377244.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
SNX16_chr8_81794583_81847185 | 81822964 | A | ATATATAT others(11): Show |
intron_variant | MODIFIER | HG00733.hp2 HG01106.hp1 HG02055.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0006a0001c0001t0015 | a0001c0001t0005g0030 a0001c0001t0005g0158 a0001c0001t0005g0159 others(8): Show |
12 | 306 | 0.0392 | 18 | c.611 others(33): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | TogoVar | |||||||
SNX19_chr11_130861250_130921479 | 130905207 | C | CCTGGAAG others(11): Show |
intron_variant | MODIFIER | HG03704.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0247 | 1 | 414 | 0.0024 | 18 | c.244 others(35): Show |
SNX19 | ENSG00000120451.11 | transcript | ENST00000265909.9 | protein_coding | 7/10 | chr11 | TogoVar | |||||||
SNX1_chr15_64090982_64149231 | 64124147 | C | CATATATA others(11): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG02559.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0013a0001c0001t0027a0001c0001t0080others(3): Show | a0001c0001t0013g0137 a0001c0001t0027g0079 a0001c0001t0027g0084 others(4): Show |
7 | 270 | 0.0259 | 18 | c.510 others(33): Show |
SNX1 | ENSG00000028528.15 | transcript | ENST00000559844.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185212491 | G | GTGTGTGT others(11): Show |
intron_variant | MODIFIER | NA18961.hp1 NA18963.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | 276 | 0.0073 | 18 | c.429 others(35): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185300840 | G | GACACACA others(11): Show |
intron_variant | MODIFIER | HG00408.hp1 HG01934.hp1 HG03540.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0001 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0058 others(2): Show |
5 | 276 | 0.0181 | 18 | c.116 others(37): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185360930 | A | AATATATA others(11): Show |
intron_variant | MODIFIER | HG02145.hp2 HG03195.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0196 a0001c0001t0001g0220 |
2 | 276 | 0.0073 | 18 | c.265 others(35): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX27_chr1_151607050_151704080 | 151641598 | G | GATATATA others(11): Show |
intron_variant | MODIFIER | HG01255.hp1 HG01516.hp2 HG02040.hp1 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0015a0001c0001t0017others(10): Show | a0001c0001t0002g0038 a0001c0001t0015g0289 a0001c0001t0015g0296 others(12): Show |
15 | 366 | 0.0410 | 18 | c.543 others(35): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SNX27_chr1_151607050_151704080 | 151652205 | G | GGGGAGAG others(11): Show |
intron_variant | MODIFIER | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0009a0001c0001t0034others(4): Show | a0001c0001t0006g0188 a0001c0001t0009g0202 a0001c0001t0034g0241 others(6): Show |
9 | 366 | 0.0246 | 18 | c.544 others(35): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 11979275 | C | CAAAAAAA others(11): Show |
intron_variant | MODIFIER | HG02257.hp2 HG02630.hp2 |
a0001 | a0001c0004a0001c0013 | a0001c0004t0079a0001c0013t0094 | a0001c0004t0079g0070 a0001c0013t0094g0126 |
2 | 176 | 0.0114 | 18 | c.7+2 others(31): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12013498 | A | AATATATA others(11): Show |
intron_variant | MODIFIER | HG01071.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0157 | 1 | 176 | 0.0057 | 18 | c.122 others(37): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12013500 | A | AAAAAAAA others(11): Show |
intron_variant | MODIFIER | NA19009.hp2 | a0001 | a0001c0003 | a0001c0003t0103 | a0001c0003t0103g0079 | 1 | 176 | 0.0057 | 18 | c.122 others(37): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12013500 | A | AAAAAATA others(11): Show |
intron_variant | MODIFIER | NA18950.hp1 | a0001 | a0001c0001 | a0001c0001t0042 | a0001c0001t0042g0015 | 1 | 176 | 0.0057 | 18 | c.122 others(37): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12013500 | A | AAAATATA others(11): Show |
intron_variant | MODIFIER | HG01496.hp2 HG03491.hp2 NA19060.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0012a0001c0001t0110a0001c0004t0095 | a0001c0001t0012g0056 a0001c0001t0110g0162 a0001c0004t0095g0151 |
3 | 176 | 0.0171 | 18 | c.122 others(37): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12013500 | A | AACATATA others(11): Show |
intron_variant | MODIFIER | NA18522.hp2 | a0001 | a0001c0002 | a0001c0002t0067 | a0001c0002t0067g0059 | 1 | 176 | 0.0057 | 18 | c.122 others(37): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12013518 | T | TATATATA others(11): Show |
intron_variant | MODIFIER | HG00673.hp1 | a0001 | a0001c0001 | a0001c0001t0050 | a0001c0001t0050g0140 | 1 | 176 | 0.0057 | 18 | c.122 others(37): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12045610 | A | ATATTATT others(11): Show |
intron_variant | MODIFIER | HG02886.hp2 NA21309.hp1 |
a0001 | a0001c0001 | a0001c0001t0017a0001c0001t0027 | a0001c0001t0017g0025 a0001c0001t0027g0082 |
2 | 176 | 0.0114 | 18 | c.429 others(33): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12118313 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG01109.hp1 | a0001 | a0001c0002 | a0001c0002t0069 | a0001c0002t0069g0017 | 1 | 176 | 0.0057 | 18 | c.140 others(37): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12179870 | G | GTTGGTAG others(11): Show |
intron_variant | MODIFIER | HG00558.hp2 HG00738.hp1 HG00741.hp2 others(30): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0008a0001c0001t0015others(24): Show | a0001c0001t0001g0153 a0001c0001t0001g0163 a0001c0001t0008g0137 others(30): Show |
33 | 176 | 0.1875 | 18 | c.159 others(39): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12179870 | G | GTTGGTGG others(11): Show |
intron_variant | MODIFIER | HG01346.hp2 | a0001 | a0001c0004 | a0001c0004t0098 | a0001c0004t0098g0045 | 1 | 176 | 0.0057 | 18 | c.159 others(39): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12339370 | C | CAAAAAAA others(11): Show |
intron_variant | MODIFIER | NA18990.hp1 | a0001 | a0001c0002 | a0001c0002t0075 | a0001c0002t0075g0129 | 1 | 176 | 0.0057 | 18 | c.178 others(39): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12380952 | C | CCATCCAT others(11): Show |
intron_variant | MODIFIER | HG01261.hp2 HG02257.hp2 HG03486.hp2 |
a0001 | a0001c0001a0001c0002a0001c0013 | a0001c0001t0002a0001c0002t0024a0001c0013t0094 | a0001c0001t0002g0169 a0001c0002t0024g0050 a0001c0013t0094g0126 |
3 | 176 | 0.0171 | 18 | c.190 others(39): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12462017 | A | ATATATAT others(11): Show |
intron_variant | MODIFIER | HG03834.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0153 | 1 | 176 | 0.0057 | 18 | c.203 others(39): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | chr16 | TogoVar | |||||||
SNX29_chr16_11971734_12579287 | 12464229 | C | CGTGTGTG others(11): Show |
intron_variant | MODIFIER | HG00639.hp2 HG02040.hp2 HG02896.hp2 others(10): Show |
a0001a0007 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0027a0001c0002t0003a0001c0002t0005others(10): Show | a0001c0001t0027g0082 a0001c0002t0003g0152 a0001c0002t0005g0168 others(10): Show |
13 | 176 | 0.0739 | 18 | c.203 others(39): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12476423 | T | TATATATA others(11): Show |
intron_variant | MODIFIER | HG00738.hp1 HG00741.hp2 |
a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0077 a0001c0003t0002g0097 |
2 | 176 | 0.0114 | 18 | c.203 others(37): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12512369 | A | AATATATA others(11): Show |
intron_variant | MODIFIER | HG02896.hp1 HG02897.hp1 |
a0001 | a0001c0004 | a0001c0004t0020 | a0001c0004t0020g0038 a0001c0004t0020g0055 |
2 | 176 | 0.0114 | 18 | c.217 others(39): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX2_chr5_122770080_122839543 | 122789474 | G | GACACACA others(11): Show |
intron_variant | MODIFIER | NA19011.hp1 NA19082.hp1 |
a0001 | a0001c0002 | a0001c0002t0006a0001c0002t0009 | a0001c0002t0006g0227 a0001c0002t0009g0232 |
2 | 372 | 0.0054 | 18 | c.109 others(35): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
SNX2_chr5_122770080_122839543 | 122806142 | G | GCACGCGC others(11): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0171 | 1 | 372 | 0.0027 | 18 | c.644 others(35): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
SNX2_chr5_122770080_122839543 | 122814753 | T | TTTTTTTT others(11): Show |
intron_variant | MODIFIER | NA18995.hp2 | a0001 | a0001c0001 | a0001c0001t0048 | a0001c0001t0048g0030 | 1 | 372 | 0.0027 | 18 | c.723 others(35): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
SNX2_chr5_122770080_122839543 | 122814753 | T | TTTTTTTT others(11): Show |
intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0095 | 1 | 372 | 0.0027 | 18 | c.723 others(35): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112775542 | T | TTGTGTGT others(11): Show |
intron_variant | MODIFIER | NA19063.hp2 NA19065.hp2 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0005 | a0001c0001t0003g0288 a0001c0001t0005g0060 |
2 | 338 | 0.0059 | 18 | c.156 others(37): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112795765 | T | TCTCACAC others(11): Show |
intron_variant | MODIFIER | HG00544.hp1 HG01346.hp2 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0247 a0001c0001t0003g0271 |
2 | 338 | 0.0059 | 18 | c.157 others(35): 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(11): Show |
intron_variant | MODIFIER | HG00423.hp2 HG01106.hp1 HG02083.hp1 others(5): Show |
a0001a0006 | a0001c0001a0001c0002a0006c0009 | a0001c0001t0001a0001c0001t0017a0001c0002t0001others(3): Show | a0001c0001t0001g0152 a0001c0001t0017g0235 a0001c0002t0001g0028 others(5): Show |
8 | 338 | 0.0237 | 18 | c.349 others(33): 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(11): Show |
intron_variant | MODIFIER | HG00621.hp2 HG02080.hp2 HG02615.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0063 a0001c0001t0002g0039 a0001c0001t0003g0192 others(1): Show |
4 | 338 | 0.0118 | 18 | c.619 others(35): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112865661 | A | ATATATAT others(11): Show |
intron_variant | MODIFIER | HG06807.hp1 | a0001 | a0001c0002 | a0001c0002t0007 | a0001c0002t0007g0326 | 1 | 338 | 0.0030 | 18 | c.125 others(37): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112865661 | A | ATATATAT others(11): Show |
intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0321 | 1 | 338 | 0.0030 | 18 | c.125 others(37): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX31_chr8_100567889_100654665 | 100641625 | C | CATATATA others(11): Show |
intron_variant | MODIFIER | HG03098.hp1 | a0004 | a0004c0004 | a0004c0004t0004 | a0004c0004t0004g0156 | 1 | 304 | 0.0033 | 18 | c.142 others(35): Show |
SNX31 | ENSG00000174226.9 | transcript | ENST00000311812.7 | protein_coding | 2/13 | chr8 | TogoVar | |||||||
SNX32_chr11_65828963_65858701 | 65839215 | A | ATTTTTTT others(11): Show |
intron_variant | MODIFIER | HG01255.hp2 HG02258.hp1 HG02572.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0030 a0001c0001t0001g0060 a0001c0001t0001g0094 others(3): Show |
7 | 390 | 0.0180 | 18 | c.36+ others(33): Show |
SNX32 | ENSG00000172803.18 | transcript | ENST00000308342.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
SNX32_chr11_65828963_65858701 | 65839223 | G | GTTTTGTT others(11): Show |
intron_variant | MODIFIER | HG03942.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0063 | 1 | 390 | 0.0026 | 18 | c.36+ others(33): Show |
SNX32 | ENSG00000172803.18 | transcript | ENST00000308342.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |