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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SNTG2_chr2_945849_1372613 | 1222005 | C | CTGTCTCT others(29): Show |
intron_variant | MODIFIER | HG03927.hp2 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0185 | 1 | 190 | 0.0053 | 36 | c.719 others(55): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
SNX10_chr7_26286862_26379383 | 26291922 | T | TGCGCGGG others(29): Show |
5_prime_UTR_variant | MODIFIER | HG01496.hp2 HG02071.hp1 NA18939.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0010a0001c0001t0015a0001c0001t0023 | a0001c0001t0010g0022a0001c0001t0010g0039a0001c0001t0010g0057others(4): Show | 7 | 390 | 0.0180 | 36 | c.-15 others(45): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/7 | 54485 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||
SNX10_chr7_26286862_26379383 | 26325306 | A | AATATATA others(29): Show |
intron_variant | MODIFIER | HG02148.hp1 HG02451.hp1 HG02683.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0086a0001c0001t0001g0224a0001c0001t0001g0225others(7): Show | 10 | 390 | 0.0256 | 36 | c.-23 others(55): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
SNX12_chrX_71054247_71073334 | 71071522 | T | TATATTTA others(29): Show |
upstream_gene_variant | MODIFIER | HG01884.hp1 HG02055.hp1 HG02280.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0010 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0056others(4): Show | 14 | 309 | 0.0453 | 36 | c.-32 others(47): Show |
SNX12 | ENSG00000147164.12 | transcript | ENST00000374274.8 | protein_coding | 3189 | chrX | TogoVar | ||||||
SNX13_chr7_17785761_17945494 | 17805250 | T | TGTGTGTG others(29): Show |
intron_variant | MODIFIER | NA18969.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0114 | 1 | 338 | 0.0030 | 36 | c.206 others(55): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | TogoVar | ||||||
SNX18_chr5_54512759_54551586 | 54513772 | A | ATATATAA others(29): Show |
upstream_gene_variant | MODIFIER | HG03017.hp2 | a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0005 | 1 | 390 | 0.0026 | 36 | c.-41 others(47): Show |
SNX18 | ENSG00000178996.14 | transcript | ENST00000381410.5 | protein_coding | 3986 | chr5 | TogoVar | ||||||
SNX18_chr5_54512759_54551586 | 54513823 | A | ATATATAA others(29): Show |
upstream_gene_variant | MODIFIER | HG02055.hp1 HG02451.hp1 HG02559.hp1 others(7): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0002a0001c0001t0006a0001c0007t0010others(1): Show | a0001c0001t0002g0049a0001c0001t0006g0023a0001c0001t0006g0050others(2): Show | 10 | 390 | 0.0256 | 36 | c.-41 others(47): Show |
SNX18 | ENSG00000178996.14 | transcript | ENST00000381410.5 | protein_coding | 3935 | chr5 | TogoVar | ||||||
SNX18_chr5_54512759_54551586 | 54513948 | A | ATATATGA others(29): Show |
upstream_gene_variant | MODIFIER | HG02109.hp2 HG02257.hp2 NA18906.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0003t0030 | a0001c0001t0002g0036a0001c0003t0030g0057 | 3 | 390 | 0.0077 | 36 | c.-40 others(47): Show |
SNX18 | ENSG00000178996.14 | transcript | ENST00000381410.5 | protein_coding | 3810 | chr5 | TogoVar | ||||||
SNX18_chr5_54512759_54551586 | 54513984 | A | ATATATGA others(29): Show |
upstream_gene_variant | MODIFIER | HG02451.hp1 HG02559.hp2 HG02970.hp1 others(3): Show |
a0001 | a0001c0001a0001c0011 | a0001c0001t0002a0001c0001t0006a0001c0011t0009 | a0001c0001t0002g0049a0001c0001t0006g0023a0001c0001t0006g0050others(1): Show | 6 | 390 | 0.0154 | 36 | c.-39 others(47): Show |
SNX18 | ENSG00000178996.14 | transcript | ENST00000381410.5 | protein_coding | 3774 | chr5 | TogoVar | ||||||
SNX18_chr5_54512759_54551586 | 54514092 | A | ATATATGA others(29): Show |
upstream_gene_variant | MODIFIER | HG01993.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0008 | 1 | 390 | 0.0026 | 36 | c.-38 others(47): Show |
SNX18 | ENSG00000178996.14 | transcript | ENST00000381410.5 | protein_coding | 3666 | chr5 | TogoVar | ||||||
SNX25_chr4_185204598_185368966 | 185241511 | A | AGAGGGAG others(29): Show |
intron_variant | MODIFIER | HG02572.hp2 HG02615.hp1 HG03130.hp1 |
a0001a0003 | a0001c0006a0003c0007 | a0001c0006t0001a0003c0007t0001 | a0001c0006t0001g0075a0001c0006t0001g0076a0003c0007t0001g0077 | 3 | 276 | 0.0109 | 36 | c.430 others(53): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
SNX25_chr4_185204598_185368966 | 185260173 | A | ATTTTATT others(29): Show |
intron_variant | MODIFIER | HG03209.hp1 NA20129.hp1 |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0256a0002c0002t0001g0257 | 2 | 276 | 0.0073 | 36 | c.731 others(53): Show |
SNX25 | ENSG00000109762.17 | transcript | ENST00000652585.2 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
SNX27_chr1_151607050_151704080 | 151681235 | C | CTTTTTTT others(29): Show |
intron_variant | MODIFIER | NA18999.hp1 | a0001 | a0001c0001 | a0001c0001t0030 | a0001c0001t0030g0210 | 1 | 366 | 0.0027 | 36 | c.115 others(55): 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(29): Show |
3_prime_UTR_variant | MODIFIER | NA18986.hp1 | a0001 | a0001c0001 | a0001c0001t0106 | a0001c0001t0106g0239 | 1 | 366 | 0.0027 | 36 | c.*20 others(47): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||
SNX29_chr16_11971734_12579287 | 12322849 | A | AGGGGACC others(29): Show |
intron_variant | MODIFIER | HG00438.hp2 HG00642.hp2 HG00673.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0002a0001c0001t0026a0001c0001t0041others(4): Show | a0001c0001t0002g0020a0001c0001t0026g0062a0001c0001t0041g0046others(4): Show | 7 | 176 | 0.0398 | 36 | c.178 others(57): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
SNX29_chr16_11971734_12579287 | 12322885 | T | TGGGGACC others(29): Show |
intron_variant | MODIFIER | HG02258.hp1 | a0001 | a0001c0002 | a0001c0002t0107 | a0001c0002t0107g0069 | 1 | 176 | 0.0057 | 36 | c.178 others(57): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
SNX29_chr16_11971734_12579287 | 12322905 | C | CGGTCACT others(29): Show |
intron_variant | MODIFIER | HG00558.hp1 HG01081.hp1 HG01109.hp2 others(18): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0006a0001c0001t0008a0001c0001t0014others(15): Show | a0001c0001t0006g0031a0001c0001t0008g0137a0001c0001t0014g0099others(18): Show | 21 | 176 | 0.1193 | 36 | c.178 others(57): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
SNX29_chr16_11971734_12579287 | 12323029 | T | TGGGGACC others(29): Show |
intron_variant | MODIFIER | NA19090.hp1 | a0001 | a0001c0002 | a0001c0002t0005 | a0001c0002t0005g0168 | 1 | 176 | 0.0057 | 36 | c.178 others(57): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
SNX29_chr16_11971734_12579287 | 12323101 | C | CGGGGACC others(29): Show |
intron_variant | MODIFIER | HG00280.hp1 | a0001 | a0001c0003 | a0001c0003t0057 | a0001c0003t0057g0105 | 1 | 176 | 0.0057 | 36 | c.178 others(57): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
SNX29_chr16_11971734_12579287 | 12323218 | C | CGGGGACC others(29): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(63): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(51): Show | a0001c0001t0001g0112a0001c0001t0001g0163a0001c0001t0004g0078others(63): Show | 66 | 176 | 0.3750 | 36 | c.178 others(57): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
SNX29_chr16_11971734_12579287 | 12393381 | G | GATTCATT others(29): Show |
intron_variant | MODIFIER | HG02451.hp1 HG02559.hp1 HG02886.hp2 |
a0001 | a0001c0001a0001c0012 | a0001c0001t0002a0001c0001t0017a0001c0012t0002 | a0001c0001t0002g0081a0001c0001t0017g0025a0001c0012t0002g0028 | 3 | 176 | 0.0171 | 36 | c.190 others(55): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
SNX29_chr16_11971734_12579287 | 12393398 | A | ATGCATGC others(29): Show |
intron_variant | MODIFIER | HG00733.hp2 | a0003 | a0003c0008 | a0003c0008t0010 | a0003c0008t0010g0145 | 1 | 176 | 0.0057 | 36 | c.190 others(55): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
SNX29_chr16_11971734_12579287 | 12393412 | G | GCATTCAT others(29): Show |
intron_variant | MODIFIER | HG02523.hp1 NA19043.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0034a0001c0003t0104 | a0001c0001t0034g0063a0001c0003t0104g0156 | 2 | 176 | 0.0114 | 36 | c.190 others(55): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
SNX29_chr16_11971734_12579287 | 12476420 | A | ATATATAT others(29): Show |
intron_variant | MODIFIER | HG04115.hp1 | a0001 | a0001c0004 | a0001c0004t0005 | a0001c0004t0005g0115 | 1 | 176 | 0.0057 | 36 | c.203 others(55): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
SNX29_chr16_11971734_12579287 | 12476421 | T | TATATATA others(29): Show |
intron_variant | MODIFIER | HG02683.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0132 | 1 | 176 | 0.0057 | 36 | c.203 others(55): Show |
SNX29 | ENSG00000048471.14 | transcript | ENST00000566228.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
SNX2_chr5_122770080_122839543 | 122806120 | G | GTGTGTGT others(29): Show |
intron_variant | MODIFIER | HG02895.hp1 | a0001 | a0001c0001 | a0001c0001t0037 | a0001c0001t0037g0352 | 1 | 372 | 0.0027 | 36 | c.644 others(53): 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(29): Show |
intron_variant | MODIFIER | HG01081.hp1 NA19081.hp2 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0050 | a0001c0001t0004g0142a0001c0001t0050g0215 | 2 | 372 | 0.0054 | 36 | c.644 others(53): 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(29): Show |
intron_variant | MODIFIER | HG02015.hp1 | a0001 | a0001c0002 | a0001c0002t0009 | a0001c0002t0009g0245 | 1 | 372 | 0.0027 | 36 | c.644 others(53): Show |
SNX2 | ENSG00000205302.7 | transcript | ENST00000379516.7 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
SNX30_chr9_112745760_112879987 | 112865661 | A | ATATATAT others(29): Show |
intron_variant | MODIFIER | HG00741.hp2 | a0002 | a0002c0003 | a0002c0003t0004 | a0002c0003t0004g0005 | 1 | 338 | 0.0030 | 36 | c.125 others(55): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
SNX30_chr9_112745760_112879987 | 112865661 | A | ATATGTGT others(29): Show |
intron_variant | MODIFIER | NA18943.hp2 | a0002 | a0002c0003 | a0002c0003t0004 | a0002c0003t0004g0002 | 1 | 338 | 0.0030 | 36 | c.125 others(55): Show |
SNX30 | ENSG00000148158.17 | transcript | ENST00000374232.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
SNX31_chr8_100567889_100654665 | 100635222 | T | TTTTATTT others(29): Show |
intron_variant | MODIFIER | HG01928.hp2 | a0003 | a0003c0003 | a0003c0003t0006 | a0003c0003t0006g0147 | 1 | 304 | 0.0033 | 36 | c.256 others(51): Show |
SNX31 | ENSG00000174226.9 | transcript | ENST00000311812.7 | protein_coding | 3/13 | chr8 | TogoVar | ||||||
SNX4_chr3_125441650_125525202 | 125495275 | T | TATATATA others(29): Show |
intron_variant | MODIFIER | HG01074.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0145 | 1 | 360 | 0.0028 | 36 | c.597 others(53): Show |
SNX4 | ENSG00000114520.11 | transcript | ENST00000251775.9 | protein_coding | 5/13 | chr3 | TogoVar | ||||||
SNX4_chr3_125441650_125525202 | 125495277 | T | TATATATA others(29): Show |
intron_variant | MODIFIER | HG02970.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0169 | 1 | 360 | 0.0028 | 36 | c.597 others(53): Show |
SNX4 | ENSG00000114520.11 | transcript | ENST00000251775.9 | protein_coding | 5/13 | chr3 | TogoVar | ||||||
SNX7_chr1_98656721_98765500 | 98763443 | A | AAAATATA others(29): Show |
downstream_gene_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0269 | 1 | 378 | 0.0027 | 36 | c.*33 others(47): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2944 | chr1 | TogoVar | ||||||
SNX7_chr1_98656721_98765500 | 98763443 | A | AATATATA others(29): Show |
downstream_gene_variant | MODIFIER | HG02922.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0323 | 1 | 378 | 0.0027 | 36 | c.*33 others(47): Show |
SNX7 | ENSG00000162627.17 | transcript | ENST00000306121.8 | protein_coding | 2944 | chr1 | TogoVar | ||||||
SNX9_chr6_157818246_157950077 | 157844587 | G | GTTTTTTT others(29): Show |
intron_variant | MODIFIER | NA19002.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0039 | 1 | 302 | 0.0033 | 36 | c.12+ others(53): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
SNX9_chr6_157818246_157950077 | 157844587 | G | GTTTTTTT others(29): Show |
intron_variant | MODIFIER | HG00642.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0027 | 1 | 302 | 0.0033 | 36 | c.12+ others(53): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
SNX9_chr6_157818246_157950077 | 157915640 | A | AAAAAAAA others(29): Show |
intron_variant | MODIFIER | NA19079.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0007 | 1 | 302 | 0.0033 | 36 | c.949 others(53): Show |
SNX9 | ENSG00000130340.17 | transcript | ENST00000392185.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
SOCS4_chr14_55022236_55054489 | 55041783 | C | CTTTTTTT others(29): Show |
intron_variant | MODIFIER | HG00323.hp1 | a0001 | a0001c0001 | a0001c0001t0033 | a0001c0001t0033g0155 | 1 | 394 | 0.0025 | 36 | c.-90 others(53): Show |
SOCS4 | ENSG00000180008.9 | transcript | ENST00000555846.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
SOCS7_chr17_38346844_38410593 | 38387133 | G | GTGTGTGT others(29): Show |
intron_variant | MODIFIER | HG00733.hp2 HG02572.hp1 HG02818.hp2 |
a0001 | a0001c0002 | a0001c0002t0011 | a0001c0002t0011g0016a0001c0002t0011g0019a0001c0002t0011g0021 | 3 | 289 | 0.0104 | 36 | c.168 others(55): Show |
SOCS7 | ENSG00000274211.6 | transcript | ENST00000612932.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
SOHLH2_chr13_36163217_36219556 | 36184460 | C | CTTTTTTT others(29): Show |
intron_variant | MODIFIER | HG03669.hp2 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0093 | 1 | 420 | 0.0024 | 36 | c.641 others(53): Show |
SOHLH2 | ENSG00000120669.16 | transcript | ENST00000379881.8 | protein_coding | 6/10 | chr13 | TogoVar | ||||||
SORBS1_chr10_95306773_95566371 | 95563407 | C | CTCAGGAG others(29): Show |
upstream_gene_variant | MODIFIER | HG02040.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0193 | 1 | 300 | 0.0033 | 36 | c.-22 others(47): Show |
SORBS1 | ENSG00000095637.23 | transcript | ENST00000371247.7 | protein_coding | 2037 | chr10 | TogoVar | ||||||
SORBS2_chr4_185580523_185817194 | 185580753 | G | GCCAGCCA others(29): Show |
downstream_gene_variant | MODIFIER | NA19074.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0126 | 1 | 312 | 0.0032 | 36 | c.*68 others(47): Show |
SORBS2 | ENSG00000154556.20 | transcript | ENST00000695409.1 | protein_coding | 4769 | chr4 | TogoVar | ||||||
SORCS1_chr10_106568663_107169706 | 107065415 | T | TTTTCTTT others(29): Show |
intron_variant | MODIFIER | HG02735.hp1 NA18995.hp1 NA19030.hp2 |
a0001 | a0001c0002a0001c0003a0001c0019 | a0001c0002t0003a0001c0003t0001a0001c0019t0001 | a0001c0002t0003g0032a0001c0003t0001g0116a0001c0019t0001g0016 | 3 | 130 | 0.0231 | 36 | c.558 others(55): Show |
SORCS1 | ENSG00000108018.17 | transcript | ENST00000263054.11 | protein_coding | 1/25 | chr10 | TogoVar | ||||||
SORCS2_chr4_7187538_7747827 | 7373478 | A | ATATATAT others(29): Show |
intron_variant | MODIFIER | NA18966.hp2 | a0001 | a0001c0002 | a0001c0002t0010 | a0001c0002t0010g0045 | 1 | 168 | 0.0060 | 36 | c.481 others(55): Show |
SORCS2 | ENSG00000184985.17 | transcript | ENST00000507866.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
SORCS2_chr4_7187538_7747827 | 7373478 | A | ATATATAT others(29): Show |
intron_variant | MODIFIER | HG02165.hp2 | a0001 | a0001c0003 | a0001c0003t0010 | a0001c0003t0010g0021 | 1 | 168 | 0.0060 | 36 | c.481 others(55): Show |
SORCS2 | ENSG00000184985.17 | transcript | ENST00000507866.6 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
SORCS2_chr4_7187538_7747827 | 7543919 | T | TCCATCCA others(29): Show |
intron_variant | MODIFIER | HG02257.hp1 | a0012 | a0012c0039 | a0012c0039t0063 | a0012c0039t0063g0064 | 1 | 168 | 0.0060 | 36 | c.648 others(55): Show |
SORCS2 | ENSG00000184985.17 | transcript | ENST00000507866.6 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
SORCS2_chr4_7187538_7747827 | 7543939 | C | CCCATCCA others(29): Show |
intron_variant | MODIFIER | HG01346.hp1 | a0014 | a0014c0024 | a0014c0024t0049 | a0014c0024t0049g0108 | 1 | 168 | 0.0060 | 36 | c.648 others(55): Show |
SORCS2 | ENSG00000184985.17 | transcript | ENST00000507866.6 | protein_coding | 3/26 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
SORCS3_chr10_104636290_105270242 | 104818360 | T | TCTTCCTT others(29): Show |
intron_variant | MODIFIER | HG01358.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0018 | 1 | 134 | 0.0075 | 36 | c.628 others(55): Show |
SORCS3 | ENSG00000156395.14 | transcript | ENST00000369701.8 | protein_coding | 1/26 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
SORCS3_chr10_104636290_105270242 | 105016155 | A | ATATATAT others(29): Show |
intron_variant | MODIFIER | HG01099.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0045 | 1 | 134 | 0.0075 | 36 | c.955 others(55): Show |
SORCS3 | ENSG00000156395.14 | transcript | ENST00000369701.8 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr10 | TogoVar |