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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SNTG1_chr8_49906407_50801692 | 50660241 | G | GGAAGGAA others(17): Show |
intron_variant | MODIFIER | HG01071.hp2 HG02055.hp1 HG02723.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0007a0001c0001t0009a0001c0001t0010others(4): Show | a0001c0001t0007g0006 a0001c0001t0009g0100 a0001c0001t0009g0101 others(6): Show |
9 | 106 | 0.0849 | 24 | c.103 others(43): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50701579 | T | TTTCTTCT others(17): Show |
intron_variant | MODIFIER | HG01884.hp1 HG02976.hp2 |
a0001 | a0001c0001 | a0001c0001t0023a0001c0001t0035 | a0001c0001t0023g0002 a0001c0001t0035g0031 |
2 | 73 | 0.0274 | 24 | c.103 others(43): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50734808 | G | GATATCTA others(17): Show |
intron_variant | MODIFIER | HG00621.hp1 NA18952.hp2 NA18992.hp1 others(1): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0003 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0098 others(1): Show |
4 | 101 | 0.0396 | 24 | c.128 others(45): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 948493 | C | CATATATA others(17): Show |
upstream_gene_variant | MODIFIER | HG02559.hp1 HG02976.hp1 |
a0004a0009 | a0004c0004a0009c0012 | a0004c0004t0001a0009c0012t0001 | a0004c0004t0001g0047 a0009c0012t0001g0066 |
2 | 51 | 0.0392 | 24 | c.-25 others(35): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 2355 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 996673 | G | GTTTTTTT others(17): Show |
intron_variant | MODIFIER | HG00438.hp2 HG02735.hp2 |
a0001a0002 | a0001c0002a0002c0003 | a0001c0002t0001a0002c0003t0001 | a0001c0002t0001g0170 a0002c0003t0001g0099 |
2 | 3 | 0.6667 | 24 | c.72+ others(41): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1031508 | T | TTTTATAT others(17): Show |
intron_variant | MODIFIER | HG03486.hp2 | a0003 | a0003c0007 | a0003c0007t0002 | a0003c0007t0002g0077 | 1 | 170 | 0.0059 | 24 | c.73- others(41): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1031528 | A | ATATATAT others(17): Show |
intron_variant | MODIFIER | HG03017.hp1 NA20300.hp2 |
a0002a0007 | a0002c0003a0007c0024 | a0002c0003t0001a0007c0024t0002 | a0002c0003t0001g0094 a0007c0024t0002g0073 |
2 | 82 | 0.0244 | 24 | c.73- others(41): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1031528 | A | ATATATAT others(17): Show |
intron_variant | MODIFIER | HG01496.hp1 HG02273.hp1 |
a0002a0006 | a0002c0003a0006c0009 | a0002c0003t0001a0006c0009t0001 | a0002c0003t0001g0029 a0006c0009t0001g0028 |
2 | 82 | 0.0244 | 24 | c.73- others(41): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1031528 | A | ATATATAT others(17): Show |
intron_variant | MODIFIER | HG02071.hp2 HG02132.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0014 a0001c0002t0001g0016 |
2 | 82 | 0.0244 | 24 | c.73- others(41): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1222109 | C | CTCTCTGT others(17): Show |
intron_variant | MODIFIER | HG00735.hp1 | a0003 | a0003c0008 | a0003c0008t0001 | a0003c0008t0001g0096 | 1 | 137 | 0.0073 | 24 | c.719 others(43): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1255863 | A | AATATATA others(17): Show |
intron_variant | MODIFIER | HG02451.hp2 HG03540.hp1 |
a0003a0015 | a0003c0026a0015c0025 | a0003c0026t0001a0015c0025t0001 | a0003c0026t0001g0097 a0015c0025t0001g0034 |
2 | 186 | 0.0108 | 24 | c.100 others(43): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNX10_chr7_26286862_26379383 | 26325306 | A | AATATATA others(17): Show |
intron_variant | MODIFIER | HG00642.hp2 HG01192.hp1 HG03017.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005 a0001c0001t0001g0136 a0001c0001t0001g0141 others(5): Show |
9 | 15 | 0.6000 | 24 | c.-23 others(43): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX11_chr17_48102766_48128601 | 48105324 | C | CTTTTTTT others(17): Show |
upstream_gene_variant | MODIFIER | HG02970.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0161 | 1 | 50 | 0.0200 | 24 | c.-25 others(35): Show |
SNX11 | ENSG00000002919.15 | transcript | ENST00000359238.7 | protein_coding | 2441 | chr17 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17805250 | T | TGTGCGTG others(17): Show |
intron_variant | MODIFIER | NA18954.hp1 | a0001 | a0001c0002 | a0001c0002t0027 | a0001c0002t0027g0300 | 1 | 252 | 0.0040 | 24 | c.206 others(43): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17805250 | T | TGTGTGTG others(17): Show |
intron_variant | MODIFIER | HG01516.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0204 | 1 | 252 | 0.0040 | 24 | c.206 others(43): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17805250 | T | TGTGTGTG others(17): Show |
intron_variant | MODIFIER | HG01069.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0209 | 1 | 252 | 0.0040 | 24 | c.206 others(43): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17805250 | T | TGTGTGTG others(17): Show |
intron_variant | MODIFIER | HG03225.hp1 NA18974.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0146 a0001c0001t0004g0186 |
2 | 253 | 0.0079 | 24 | c.206 others(43): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17805250 | T | TGTGTGTG others(17): Show |
intron_variant | MODIFIER | NA19010.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0290 | 1 | 252 | 0.0040 | 24 | c.206 others(43): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17805250 | T | TGTGTGTG others(17): Show |
intron_variant | MODIFIER | HG02698.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0213 | 1 | 252 | 0.0040 | 24 | c.206 others(43): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17805250 | T | TGTGTGTG others(17): Show |
intron_variant | MODIFIER | HG01243.hp1 NA18979.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0002t0002 | a0001c0001t0004g0114 a0001c0002t0002g0059 |
2 | 253 | 0.0079 | 24 | c.206 others(43): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | TogoVar | |||||||
SNX14_chr6_85500496_85598858 | 85588575 | C | CTAAATAA others(17): Show |
intron_variant | MODIFIER | HG03017.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0195 | 1 | 186 | 0.0054 | 24 | c.140 others(41): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | TogoVar | |||||||
SNX15_chr11_65022439_65045572 | 65039029 | C | CTTTTTTT others(17): Show |
intron_variant | MODIFIER | HG00423.hp1 HG00642.hp1 HG01361.hp1 others(14): Show |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0012 | a0001c0002t0002g0003 a0001c0002t0002g0046 a0001c0002t0002g0119 others(2): Show |
17 | 173 | 0.0983 | 24 | c.922 others(39): Show |
SNX15 | ENSG00000110025.13 | transcript | ENST00000377244.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
SNX18_chr5_54512759_54551586 | 54513668 | T | TATATATA others(17): Show |
upstream_gene_variant | MODIFIER | NA19087.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0001 | 1 | 384 | 0.0026 | 24 | c.-42 others(35): Show |
SNX18 | ENSG00000178996.14 | transcript | ENST00000381410.5 | protein_coding | 4090 | chr5 | TogoVar | |||||||
SNX1_chr15_64090982_64149231 | 64124147 | C | CATATATA others(17): Show |
intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0160 | 1 | 7 | 0.1429 | 24 | c.510 others(39): Show |
SNX1 | ENSG00000028528.15 | transcript | ENST00000559844.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
SNX1_chr15_64090982_64149231 | 64140983 | T | TGATAGAT others(17): Show |
3_prime_UTR_variant | MODIFIER | HG04184.hp1 HG04204.hp1 NA18953.hp2 others(1): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0002a0001c0001t0018a0001c0008t0002 | a0001c0001t0002g0097 a0001c0001t0018g0006 a0001c0008t0002g0153 |
4 | 29 | 0.1379 | 24 | c.*33 others(35): Show |
SNX1 | ENSG00000028528.15 | transcript | ENST00000559844.6 | protein_coding | 15/15 | 3409 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
SNX25_chr4_185204598_185368966 | 185300839 | T | TCACACAC others(17): Show |
intron_variant | MODIFIER | HG02922.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0013 | 1 | 273 | 0.0037 | 24 | c.116 others(43): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 6/18 | chr4 | TogoVar | |||||||
SNX25_chr4_185204598_185368966 | 185300840 | G | GACACACA others(17): Show |
intron_variant | MODIFIER | HG02148.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0082 | 1 | 49 | 0.0204 | 24 | c.116 others(43): 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(17): Show |
intron_variant | MODIFIER | HG02258.hp1 | a0003 | a0003c0007 | a0003c0007t0001 | a0003c0007t0001g0184 | 1 | 152 | 0.0066 | 24 | c.265 others(41): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185360950 | T | TATATATA others(17): Show |
intron_variant | MODIFIER | NA19085.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0107 | 1 | 250 | 0.0040 | 24 | c.265 others(41): 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(17): Show |
intron_variant | MODIFIER | HG03195.hp2 HG03688.hp1 NA19012.hp1 |
a0001 | a0001c0001 | a0001c0001t0020a0001c0001t0036a0001c0001t0100 | a0001c0001t0020g0075 a0001c0001t0036g0305 a0001c0001t0100g0096 |
3 | 14 | 0.2143 | 24 | c.543 others(41): 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(17): Show |
intron_variant | MODIFIER | NA18962.hp2 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0247 | 1 | 134 | 0.0075 | 24 | c.544 others(41): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SNX27_chr1_151607050_151704080 | 151681235 | C | CTTTTTTT others(17): Show |
intron_variant | MODIFIER | HG00738.hp2 HG02523.hp2 NA18949.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(1): Show | a0001c0001t0001g0190 a0001c0001t0001g0210 a0001c0001t0001g0223 others(4): Show |
7 | 125 | 0.0560 | 24 | c.115 others(43): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SNX27_chr1_151607050_151704080 | 151696498 | T | TTTCTTTC others(17): Show |
3_prime_UTR_variant | MODIFIER | HG00673.hp1 HG02273.hp1 HG03834.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0008 | a0001c0001t0001g0205 a0001c0001t0001g0267 a0001c0001t0001g0273 others(3): Show |
6 | 248 | 0.0242 | 24 | c.*20 others(35): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2113 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
SNX27_chr1_151607050_151704080 | 151696498 | T | TTTCTTTC others(17): Show |
3_prime_UTR_variant | MODIFIER | HG00280.hp2 HG01516.hp1 HG01978.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0091 | a0001c0001t0001g0195 a0001c0001t0001g0212 a0001c0001t0001g0217 others(4): Show |
7 | 249 | 0.0281 | 24 | c.*20 others(35): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
SNX29_chr16_11971734_12579287 | 12013498 | A | AATATATA others(17): Show |
intron_variant | MODIFIER | NA18986.hp1 | a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0161 | 1 | 161 | 0.0062 | 24 | c.122 others(43): 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(17): Show |
intron_variant | MODIFIER | HG00438.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0020 | 1 | 54 | 0.0185 | 24 | c.122 others(43): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12063366 | C | CTTTTTTT others(17): Show |
intron_variant | MODIFIER | HG02015.hp2 HG02622.hp2 |
a0001 | a0001c0003a0001c0004 | a0001c0003t0002a0001c0004t0005 | a0001c0003t0002g0119 a0001c0004t0005g0171 |
2 | 19 | 0.1053 | 24 | c.124 others(43): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12464229 | C | CGTGTGTG others(17): Show |
intron_variant | MODIFIER | HG00673.hp2 | a0001 | a0001c0002 | a0001c0002t0087 | a0001c0002t0087g0073 | 1 | 121 | 0.0083 | 24 | c.203 others(45): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX29_chr16_11971734_12579287 | 12476397 | T | TATACATA others(17): Show |
intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0001 | a0001c0001t0053 | a0001c0001t0053g0121 | 1 | 167 | 0.0060 | 24 | c.203 others(43): 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(17): Show |
intron_variant | MODIFIER | HG00741.hp1 | a0001 | a0001c0002 | a0001c0002t0086 | a0001c0002t0086g0018 | 1 | 54 | 0.0185 | 24 | c.217 others(43): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNX2_chr5_122770080_122839543 | 122806142 | G | GCGCGCAC others(17): Show |
intron_variant | MODIFIER | HG01070.hp1 | a0001 | a0001c0001 | a0001c0001t0046 | a0001c0001t0046g0152 | 1 | 15 | 0.0667 | 24 | c.644 others(41): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
SNX2_chr5_122770080_122839543 | 122806142 | G | GCGCGCAC others(17): Show |
intron_variant | MODIFIER | HG02809.hp1 | a0001 | a0001c0007 | a0001c0007t0020 | a0001c0007t0020g0231 | 1 | 15 | 0.0667 | 24 | c.644 others(41): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
SNX2_chr5_122770080_122839543 | 122806142 | G | GCGCGCAC others(17): Show |
intron_variant | MODIFIER | HG00558.hp1 HG00738.hp2 HG02280.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0021a0001c0001t0028 | a0001c0001t0004g0156 a0001c0001t0004g0159 a0001c0001t0004g0173 others(4): Show |
7 | 21 | 0.3333 | 24 | c.644 others(41): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
SNX2_chr5_122770080_122839543 | 122806142 | G | GCGCGCGC others(17): Show |
intron_variant | MODIFIER | HG02809.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0148 | 1 | 15 | 0.0667 | 24 | c.644 others(41): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112817401 | C | CTTTTTTT others(17): Show |
intron_variant | MODIFIER | HG02300.hp1 HG03579.hp2 NA18954.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0002t0001 | a0001c0001t0001g0218 a0001c0001t0003g0302 a0001c0002t0001g0030 |
3 | 10 | 0.3000 | 24 | c.349 others(39): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX30_chr9_112745760_112879987 | 112865661 | A | ATATATAT others(17): Show |
intron_variant | MODIFIER | NA19011.hp2 | a0001 | a0001c0002 | a0001c0002t0027 | a0001c0002t0027g0333 | 1 | 76 | 0.0132 | 24 | c.125 others(43): 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(17): Show |
intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0002 | a0001c0002t0007 | a0001c0002t0007g0324 | 1 | 76 | 0.0132 | 24 | c.125 others(43): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
SNX31_chr8_100567889_100654665 | 100581319 | C | CTATATAT others(17): Show |
intron_variant | MODIFIER | HG02896.hp1 HG02897.hp2 |
a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0182 a0003c0003t0001g0186 |
2 | 284 | 0.0070 | 24 | c.117 others(43): Show |
SNX31 | ENSG00000174226.9 | transcript | ENST00000311812.7 | protein_coding | 12/13 | chr8 | TogoVar | |||||||
SNX31_chr8_100567889_100654665 | 100581327 | A | ATATATAT others(17): Show |
intron_variant | MODIFIER | HG02280.hp1 | a0003 | a0003c0003 | a0003c0003t0003 | a0003c0003t0003g0177 | 1 | 264 | 0.0038 | 24 | c.117 others(43): Show |
SNX31 | ENSG00000174226.9 | transcript | ENST00000311812.7 | protein_coding | 12/13 | chr8 | TogoVar | |||||||
SNX31_chr8_100567889_100654665 | 100635222 | T | TTTTATTT others(17): Show |
intron_variant | MODIFIER | HG00621.hp1 HG01099.hp1 HG01175.hp1 others(14): Show |
a0003a0005a0007others(1): Show | a0003c0003a0005c0005a0007c0007others(1): Show | a0003c0003t0004a0003c0003t0005a0003c0003t0006others(7): Show | a0003c0003t0004g0145 a0003c0003t0005g0047 a0003c0003t0005g0048 others(13): Show |
17 | 256 | 0.0664 | 24 | c.256 others(39): Show |
SNX31 | ENSG00000174226.9 | transcript | ENST00000311812.7 | protein_coding | 3/13 | chr8 | TogoVar |