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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SNRNP48_chr6_7585198_7616967 | 7608722 | A | ATATTACT others(13): Show |
intron_variant | MODIFIER | HG00733.hp2 HG00735.hp1 HG01099.hp2 others(9): Show |
a0001 | a0001c0004 | a0001c0004t0005 | a0001c0004t0005g0019 a0001c0004t0005g0040 a0001c0004t0005g0041 others(3): Show |
12 | 426 | 0.0282 | 20 | c.972 others(33): Show |
SNRNP48 | ENSG00000168566.13 | transcript | ENST00000342415.6 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
SNRPA1_chr15_101276510_101300248 | 101289925 | C | CAAAAAAA others(13): Show |
intron_variant | MODIFIER | HG01071.hp2 HG01346.hp2 HG02486.hp2 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0010 a0001c0001t0001g0072 a0001c0001t0001g0082 others(3): Show |
11 | 442 | 0.0249 | 20 | c.309 others(37): Show |
SNRPA1 | ENSG00000131876.18 | transcript | ENST00000254193.11 | protein_coding | 3/8 | chr15 | TogoVar | |||||||
SNRPA1_chr15_101276510_101300248 | 101297503 | T | TCTTTTAT others(13): Show |
upstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(236): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0010others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(4): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
239 | 442 | 0.5407 | 20 | c.-23 others(31): Show |
SNRPA1 | ENSG00000131876.18 | transcript | ENST00000254193.11 | protein_coding | 2256 | chr15 | TogoVar | |||||||
SNRPD3_chr22_24550999_24579971 | 24561064 | C | CTTTTTTT others(13): Show |
intron_variant | MODIFIER | HG02683.hp2 NA18946.hp2 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0236 a0001c0002t0002g0259 |
2 | 400 | 0.0050 | 20 | c.126 others(37): Show |
SNRPD3 | ENSG00000100028.12 | transcript | ENST00000215829.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
SNTB1_chr8_120530756_120817046 | 120654039 | C | CAAAAAAA others(13): Show |
intron_variant | MODIFIER | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0179 a0001c0001t0002g0076 a0001c0001t0003g0021 others(4): Show |
7 | 254 | 0.0276 | 20 | c.789 others(39): Show |
SNTB1 | ENSG00000172164.15 | transcript | ENST00000517992.2 | protein_coding | 2/6 | chr8 | TogoVar | |||||||
SNTB1_chr8_120530756_120817046 | 120738545 | T | TTTCCTTC others(13): Show |
intron_variant | MODIFIER | HG01346.hp2 HG02040.hp2 HG03579.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0051 a0001c0001t0001g0151 a0001c0001t0002g0155 others(1): Show |
4 | 254 | 0.0158 | 20 | c.572 others(39): Show |
SNTB1 | ENSG00000172164.15 | transcript | ENST00000517992.2 | protein_coding | 1/6 | chr8 | TogoVar | |||||||
SNTB2_chr16_69182164_69314052 | 69199595 | C | CAAAAAAA others(13): Show |
intron_variant | MODIFIER | HG01169.hp1 HG02280.hp1 HG02486.hp2 others(12): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0006a0001c0001t0013a0001c0001t0016others(2): Show | a0001c0001t0006g0052 a0001c0001t0006g0054 a0001c0001t0006g0059 others(12): Show |
15 | 218 | 0.0688 | 20 | c.580 others(39): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
SNTB2_chr16_69182164_69314052 | 69311878 | G | GCTCGCTC others(13): Show |
downstream_gene_variant | MODIFIER | NA19077.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0187 | 1 | 218 | 0.0046 | 20 | c.*10 others(33): Show |
SNTB2 | ENSG00000168807.17 | transcript | ENST00000336278.9 | protein_coding | 2827 | chr16 | TogoVar | |||||||
SNTG1_chr8_49906407_50801692 | 49938557 | G | GTTTTCTT others(13): Show |
intron_variant | MODIFIER | HG01192.hp2 HG02622.hp2 HG03098.hp2 others(1): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0033a0001c0002t0044a0001c0002t0045others(1): Show | a0001c0001t0033g0056 a0001c0002t0044g0047 a0001c0002t0045g0046 others(1): Show |
4 | 106 | 0.0377 | 20 | c.-10 others(41): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 49938557 | G | GTTTTCTT others(13): Show |
intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0002 | a0001c0002t0006 | a0001c0002t0006g0054 | 1 | 106 | 0.0094 | 20 | c.-10 others(41): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50053623 | T | TTGTGTGT others(13): Show |
intron_variant | MODIFIER | HG00621.hp2 HG02300.hp1 HG03490.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0005a0001c0001t0013others(1): Show | a0001c0001t0003g0020 a0001c0001t0005g0018 a0001c0001t0005g0022 others(4): Show |
7 | 106 | 0.0660 | 20 | c.-10 others(43): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50115567 | C | CAAAAAAA others(13): Show |
intron_variant | MODIFIER | NA20300.hp1 | a0001 | a0001c0001 | a0001c0001t0037 | a0001c0001t0037g0034 | 1 | 106 | 0.0094 | 20 | c.-10 others(41): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50115576 | A | AAAAAAAA others(13): Show |
intron_variant | MODIFIER | HG02698.hp1 NA18944.hp1 NA19068.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0002t0001 | a0001c0001t0002g0067 a0001c0001t0004g0078 a0001c0002t0001g0077 |
3 | 106 | 0.0283 | 20 | c.-10 others(41): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50550693 | G | GTGTGTGT others(13): Show |
intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0002 | a0001c0002t0044 | a0001c0002t0044g0047 | 1 | 106 | 0.0094 | 20 | c.681 others(37): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50570226 | T | TTTTTATT others(13): Show |
intron_variant | MODIFIER | HG01243.hp2 HG01884.hp2 HG02055.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0010others(7): Show | a0001c0001t0002g0017 a0001c0001t0003g0007 a0001c0001t0010g0030 others(7): Show |
10 | 106 | 0.0943 | 20 | c.810 others(39): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50570226 | T | TTTTTTTT others(13): Show |
intron_variant | MODIFIER | HG01192.hp2 | a0001 | a0001c0001 | a0001c0001t0033 | a0001c0001t0033g0056 | 1 | 106 | 0.0094 | 20 | c.810 others(39): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50570276 | A | ATTTTATT others(13): Show |
intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0026 | 1 | 106 | 0.0094 | 20 | c.810 others(39): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
SNTG1_chr8_49906407_50801692 | 50701618 | C | CTTCTTCT others(13): Show |
intron_variant | MODIFIER | HG00280.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0094 | 1 | 106 | 0.0094 | 20 | c.103 others(39): Show |
SNTG1 | ENSG00000147481.17 | transcript | ENST00000642720.2 | protein_coding | 15/18 | chr8 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 996673 | G | GTTTTTTT others(13): Show |
intron_variant | MODIFIER | HG03540.hp2 NA18942.hp2 |
a0001a0008 | a0001c0002a0008c0011 | a0001c0002t0001a0008c0011t0001 | a0001c0002t0001g0084 a0008c0011t0001g0188 |
2 | 190 | 0.0105 | 20 | c.72+ others(37): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1051157 | T | TCCCCCTT others(13): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG01074.hp1 others(53): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0002a0002c0003others(16): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(20): Show | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0024 others(53): Show |
56 | 190 | 0.2947 | 20 | c.73- others(37): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1051166 | C | CTTCCTCC others(13): Show |
intron_variant | MODIFIER | HG00099.hp1 HG02109.hp1 HG02109.hp2 others(5): Show |
a0002a0003a0007others(2): Show | a0002c0003a0003c0008a0007c0017others(2): Show | a0002c0003t0001a0003c0008t0002a0007c0017t0001others(2): Show | a0002c0003t0001g0138 a0002c0003t0001g0139 a0003c0008t0002g0072 others(5): Show |
8 | 190 | 0.0421 | 20 | c.73- others(37): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1221909 | G | GTCTCTCT others(13): Show |
intron_variant | MODIFIER | HG02895.hp2 HG03453.hp2 NA20300.hp2 |
a0001a0007 | a0001c0002a0007c0017a0007c0024 | a0001c0002t0001a0007c0017t0001a0007c0024t0002 | a0001c0002t0001g0041 a0007c0017t0001g0105 a0007c0024t0002g0073 |
3 | 190 | 0.0158 | 20 | c.719 others(39): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1222073 | G | GTCTCTCT others(13): Show |
intron_variant | MODIFIER | NA21309.hp1 | a0006 | a0006c0009 | a0006c0009t0001 | a0006c0009t0001g0050 | 1 | 190 | 0.0053 | 20 | c.719 others(39): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1255875 | T | TATATATA others(13): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(18): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(2): Show | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0058 others(18): Show |
21 | 190 | 0.1105 | 20 | c.100 others(39): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1255911 | T | TATATATA others(13): Show |
intron_variant | MODIFIER | HG02735.hp2 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0099 | 1 | 190 | 0.0053 | 20 | c.100 others(39): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1321865 | T | TCTCCCTC others(13): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(105): Show |
a0001a0003a0004others(14): Show | a0001c0001a0001c0002a0003c0007others(22): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(26): Show | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0024 others(105): Show |
108 | 190 | 0.5684 | 20 | c.148 others(39): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1321868 | T | TCCTCCCT others(13): Show |
intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0084 | 1 | 190 | 0.0053 | 20 | c.148 others(39): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTN_chr3_63647675_63670212 | 63669415 | G | GTGTTTTG others(13): Show |
downstream_gene_variant | MODIFIER | NA18961.hp2 NA18966.hp1 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0003 | 2 | 450 | 0.0044 | 20 | c.*53 others(31): Show |
SNTN | ENSG00000188817.8 | transcript | ENST00000343837.8 | protein_coding | 4204 | chr3 | TogoVar | |||||||
SNX10_chr7_26286862_26379383 | 26325306 | A | AATATATA others(13): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00609.hp1 others(27): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0089 a0001c0001t0001g0100 a0001c0001t0001g0102 others(27): Show |
30 | 390 | 0.0769 | 20 | c.-23 others(39): Show |
SNX10 | ENSG00000086300.17 | transcript | ENST00000338523.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
SNX13_chr7_17785761_17945494 | 17801009 | C | CATATATA others(13): Show |
intron_variant | MODIFIER | HG01081.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0153 | 1 | 338 | 0.0030 | 20 | c.229 others(37): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17801016 | A | ATATATAT others(13): Show |
intron_variant | MODIFIER | HG02055.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0190 | 1 | 338 | 0.0030 | 20 | c.229 others(37): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17801022 | A | ATATATAT others(13): Show |
intron_variant | MODIFIER | HG02976.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0191 | 1 | 338 | 0.0030 | 20 | c.229 others(37): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 22/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17805211 | T | TTGTGTGT others(13): Show |
intron_variant | MODIFIER | HG02922.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0050 | 1 | 338 | 0.0030 | 20 | c.206 others(39): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17805250 | T | TGTGTGCG others(13): Show |
intron_variant | MODIFIER | HG01169.hp2 HG01952.hp2 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0280 a0001c0002t0002g0313 |
2 | 338 | 0.0059 | 20 | c.206 others(39): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17805250 | T | TGTGTGTG others(13): Show |
intron_variant | MODIFIER | HG02647.hp2 | a0001 | a0001c0001 | a0001c0001t0021 | a0001c0001t0021g0136 | 1 | 338 | 0.0030 | 20 | c.206 others(39): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17805250 | T | TGTGTGTG others(13): Show |
intron_variant | MODIFIER | HG00735.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0118 | 1 | 338 | 0.0030 | 20 | c.206 others(39): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17805250 | T | TGTGTGTG others(13): Show |
intron_variant | MODIFIER | HG01928.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0029 | 1 | 338 | 0.0030 | 20 | c.206 others(39): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17805250 | T | TGTGTGTG others(13): Show |
intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0228 | 1 | 338 | 0.0030 | 20 | c.206 others(39): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17805254 | T | TGTGCGTG others(13): Show |
intron_variant | MODIFIER | HG01978.hp2 | a0001 | a0001c0001 | a0001c0001t0029 | a0001c0001t0029g0041 | 1 | 338 | 0.0030 | 20 | c.206 others(39): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17805254 | T | TGTGTGTG others(13): Show |
intron_variant | MODIFIER | HG02135.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0112 | 1 | 338 | 0.0030 | 20 | c.206 others(39): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 20/25 | chr7 | TogoVar | |||||||
SNX13_chr7_17785761_17945494 | 17825257 | A | AACTAGAC others(13): Show |
intron_variant | MODIFIER | NA18974.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0188 | 1 | 338 | 0.0030 | 20 | c.170 others(37): Show |
SNX13 | ENSG00000071189.21 | transcript | ENST00000428135.7 | protein_coding | 17/25 | chr7 | TogoVar | |||||||
SNX14_chr6_85500496_85598858 | 85539935 | T | TTTTTATT others(13): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG01070.hp1 others(30): Show |
a0001a0006 | a0001c0001a0001c0010a0006c0008 | a0001c0001t0001a0001c0010t0001a0006c0008t0001 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0014 others(28): Show |
33 | 360 | 0.0917 | 20 | c.144 others(39): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | TogoVar | |||||||
SNX14_chr6_85500496_85598858 | 85588575 | C | CTAAATAA others(13): Show |
intron_variant | MODIFIER | HG02647.hp1 HG03654.hp2 HG03688.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0193 others(1): Show |
4 | 360 | 0.0111 | 20 | c.140 others(37): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | TogoVar | |||||||
SNX15_chr11_65022439_65045572 | 65025779 | C | CTTTTTTT others(13): Show |
upstream_gene_variant | MODIFIER | HG02818.hp2 HG02970.hp1 NA18522.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0009 a0001c0002t0001g0133 |
3 | 338 | 0.0089 | 20 | c.-17 others(31): Show |
SNX15 | ENSG00000110025.13 | transcript | ENST00000377244.8 | protein_coding | 1659 | chr11 | TogoVar | |||||||
SNX15_chr11_65022439_65045572 | 65039029 | C | CTTTTTTT others(13): Show |
intron_variant | MODIFIER | HG02280.hp2 HG02615.hp2 HG02622.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0002t0002a0001c0002t0004 | a0001c0001t0004g0059 a0001c0001t0004g0068 a0001c0001t0004g0136 others(3): Show |
6 | 338 | 0.0178 | 20 | c.922 others(35): Show |
SNX15 | ENSG00000110025.13 | transcript | ENST00000377244.8 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
SNX16_chr8_81794583_81847185 | 81822962 | A | ATATATAT others(13): Show |
intron_variant | MODIFIER | HG02922.hp1 HG03041.hp1 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0152 a0001c0001t0005g0164 |
2 | 306 | 0.0065 | 20 | c.611 others(35): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | TogoVar | |||||||
SNX16_chr8_81794583_81847185 | 81822964 | A | ATATATAT others(13): Show |
intron_variant | MODIFIER | HG00639.hp2 HG00738.hp2 HG01192.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0029 a0001c0001t0005g0146 a0001c0001t0005g0156 others(1): Show |
5 | 306 | 0.0163 | 20 | c.611 others(35): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | TogoVar | |||||||
SNX18_chr5_54512759_54551586 | 54512874 | C | CCTTCCTT others(13): Show |
upstream_gene_variant | MODIFIER | HG02622.hp1 NA21309.hp2 |
a0001 | a0001c0008 | a0001c0008t0009 | a0001c0008t0009g0198 a0001c0008t0009g0199 |
2 | 390 | 0.0051 | 20 | c.-50 others(31): Show |
SNX18 | ENSG00000178996.14 | transcript | ENST00000381410.5 | protein_coding | 4884 | chr5 | TogoVar | |||||||
SNX18_chr5_54512759_54551586 | 54520511 | G | GGCAGGGA others(13): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(189): Show |
a0001a0002a0006others(4): Show | a0001c0002a0001c0003a0001c0004others(10): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0006others(44): Show | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0011 others(130): Show |
192 | 390 | 0.4923 | 20 | c.162 others(37): Show |
SNX18 | ENSG00000178996.14 | transcript | ENST00000381410.5 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
SNX1_chr15_64090982_64149231 | 64124147 | C | CATATATA others(13): Show |
intron_variant | MODIFIER | HG02572.hp2 HG02717.hp1 HG03017.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0005a0001c0002t0021others(3): Show | a0001c0001t0003g0111 a0001c0001t0005g0114 a0001c0002t0021g0212 others(3): Show |
6 | 270 | 0.0222 | 20 | c.510 others(35): Show |
SNX1 | ENSG00000028528.15 | transcript | ENST00000559844.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr15 | TogoVar |