view | 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 | 1127128 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
a0001a0002a0003others(19): Show | a0001c0001a0001c0002a0002c0003others(32): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(40): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(185): Show | 188 | 190 | 0.9895 | -1 | c.326 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1127250 | TA | T | intron_variant | MODIFIER | HG01109.hp2 HG02486.hp1 HG02572.hp1 others(3): Show |
a0002a0003a0006others(1): Show | a0002c0005a0003c0007a0006c0010others(1): Show | a0002c0005t0001a0003c0007t0001a0003c0007t0002others(2): Show | a0002c0005t0001g0101a0003c0007t0001g0008a0003c0007t0001g0104others(3): Show | 6 | 190 | 0.0316 | -1 | c.326 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1128170 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(110): Show |
a0001a0002a0003others(13): Show | a0001c0001a0001c0002a0002c0003others(24): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(26): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(110): Show | 113 | 190 | 0.5947 | -1 | c.326 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1140816 | GA | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
a0001a0002a0003others(19): Show | a0001c0001a0001c0002a0002c0003others(32): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(40): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(185): Show | 188 | 190 | 0.9895 | -1 | c.411 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1142502 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): Show |
a0001a0002a0003others(16): Show | a0001c0001a0001c0002a0002c0003others(26): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(31): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(128): Show | 131 | 190 | 0.6895 | -1 | c.411 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1145126 | TA | T | intron_variant | MODIFIER | HG01169.hp2 HG02145.hp2 HG02451.hp1 others(6): Show |
a0001a0004a0005 | a0001c0002a0004c0004a0005c0006 | a0001c0002t0001a0001c0002t0002a0004c0004t0001others(1): Show | a0001c0002t0001g0109a0001c0002t0002g0076a0004c0004t0001g0116others(6): Show | 9 | 190 | 0.0474 | -1 | c.411 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1145288 | GA | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
a0001a0002a0003others(17): Show | a0001c0001a0001c0002a0002c0003others(27): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(34): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(147): Show | 150 | 190 | 0.7895 | -1 | c.411 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1148836 | AG | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
a0001a0002a0003others(20): Show | a0001c0001a0001c0002a0002c0003others(30): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(38): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(170): Show | 173 | 190 | 0.9105 | -1 | c.411 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1153124 | CA | C | intron_variant | MODIFIER | HG00438.hp2 HG00673.hp1 HG01516.hp2 others(23): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0002a0002c0005others(14): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(15): Show | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0002t0001g0115others(23): Show | 26 | 190 | 0.1368 | -1 | c.412 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1159145 | TG | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(116): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0002a0002c0003others(23): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(29): Show | a0001c0001t0001g0038a0001c0001t0001g0056a0001c0001t0001g0057others(116): Show | 119 | 190 | 0.6263 | -1 | c.412 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1167752 | CT | C | intron_variant | MODIFIER | HG02451.hp2 HG02647.hp1 HG02970.hp1 others(1): Show |
a0003a0011a0014others(1): Show | a0003c0026a0011c0018a0014c0035others(1): Show | a0003c0026t0001a0011c0018t0001a0014c0035t0001others(1): Show | a0003c0026t0001g0097a0011c0018t0001g0045a0014c0035t0001g0071others(1): Show | 4 | 190 | 0.0211 | -1 | c.499 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 7/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1170623 | TC | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(57): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0002a0002c0003others(14): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(15): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(57): Show | 60 | 190 | 0.3158 | -1 | c.500 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1174273 | GA | G | intron_variant | MODIFIER | HG01169.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
a0003a0005a0006others(1): Show | a0003c0007a0005c0006a0006c0009others(1): Show | a0003c0007t0001a0005c0006t0001a0006c0009t0001others(1): Show | a0003c0007t0001g0108a0005c0006t0001g0081a0005c0006t0001g0082others(5): Show | 8 | 190 | 0.0421 | -1 | c.591 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1176650 | GA | G | intron_variant | MODIFIER | HG02486.hp1 HG02615.hp1 HG02615.hp2 others(11): Show |
a0001a0003a0004others(4): Show | a0001c0001a0003c0007a0004c0004others(4): Show | a0001c0001t0001a0003c0007t0001a0003c0007t0002others(5): Show | a0001c0001t0001g0136a0003c0007t0001g0008a0003c0007t0001g0080others(11): Show | 14 | 190 | 0.0737 | -1 | c.591 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1186165 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
a0001a0002a0003others(20): Show | a0001c0001a0001c0002a0002c0003others(32): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(39): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(182): Show | 185 | 190 | 0.9737 | -1 | c.591 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 8/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1189387 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(56): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0002c0003others(13): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(14): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(56): Show | 59 | 190 | 0.3105 | -1 | c.591 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 8/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1194514 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(79): Show |
a0001a0002a0003others(11): Show | a0001c0001a0002c0003a0002c0005others(16): Show | a0001c0001t0001a0002c0003t0001a0002c0005t0001others(19): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(79): Show | 82 | 190 | 0.4316 | -1 | c.592 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1195895 | GA | G | intron_variant | MODIFIER | HG02486.hp1 HG02615.hp1 HG03225.hp2 others(2): Show |
a0003a0005 | a0003c0007a0005c0015 | a0003c0007t0001a0003c0007t0002a0005c0015t0001 | a0003c0007t0001g0008a0003c0007t0001g0104a0003c0007t0002g0075others(2): Show | 5 | 190 | 0.0263 | -1 | c.592 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1199113 | CA | C | intron_variant | MODIFIER | HG02559.hp2 HG02615.hp2 |
a0005a0018 | a0005c0015a0018c0023 | a0005c0015t0001a0018c0023t0001 | a0005c0015t0001g0103a0018c0023t0001g0048 | 2 | 190 | 0.0105 | -1 | c.592 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 8/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1207418 | GT | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
a0001a0002a0003others(20): Show | a0001c0001a0001c0002a0002c0003others(32): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(39): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(180): Show | 183 | 190 | 0.9632 | -1 | c.592 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1208982 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(54): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0002a0002c0003others(13): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(15): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(54): Show | 57 | 190 | 0.3000 | -1 | c.592 others(8): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1215079 | GA | G | intron_variant | MODIFIER | HG00673.hp2 HG01169.hp2 HG01361.hp1 others(47): Show |
a0003a0004a0005others(4): Show | a0003c0007a0004c0004a0004c0014others(9): Show | a0003c0007t0001a0003c0007t0002a0004c0004t0001others(12): Show | a0003c0007t0001g0008a0003c0007t0001g0104a0003c0007t0002g0075others(47): Show | 50 | 190 | 0.2632 | -1 | c.719 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1219348 | GC | G | intron_variant | MODIFIER | HG01109.hp1 HG01169.hp1 |
a0001a0002 | a0001c0002a0002c0003 | a0001c0002t0001a0002c0003t0001 | a0001c0002t0001g0145a0002c0003t0001g0021 | 2 | 190 | 0.0105 | -1 | c.719 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1221556 | TC | T | intron_variant | MODIFIER | HG02451.hp2 HG02572.hp1 HG03579.hp2 |
a0005a0009a0019 | a0005c0006a0009c0013a0019c0025 | a0005c0006t0001a0009c0013t0001a0019c0025t0001 | a0005c0006t0001g0086a0009c0013t0001g0042a0019c0025t0001g0034 | 3 | 190 | 0.0158 | -1 | c.719 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1221558 | CT | C | intron_variant | MODIFIER | HG00438.hp2 HG00673.hp1 HG01074.hp1 others(23): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0002c0003others(6): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(7): Show | a0001c0001t0001g0063a0001c0001t0001g0123a0001c0001t0001g0124others(23): Show | 26 | 190 | 0.1368 | -1 | c.719 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1221622 | CT | C | intron_variant | MODIFIER | HG00642.hp2 HG01257.hp1 HG02148.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0078a0001c0001t0001g0178a0001c0001t0001g0179 | 3 | 190 | 0.0158 | -1 | c.719 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1221623 | TC | T | intron_variant | MODIFIER | HG03239.hp2 HG03654.hp1 NA21309.hp1 |
a0004a0006 | a0004c0004a0006c0009 | a0004c0004t0001a0006c0009t0001 | a0004c0004t0001g0065a0004c0004t0001g0177a0006c0009t0001g0050 | 3 | 190 | 0.0158 | -1 | c.719 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1221624 | CG | C | intron_variant | MODIFIER | HG00438.hp2 HG00673.hp1 HG00735.hp2 others(52): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0002a0002c0003others(18): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(21): Show | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0025others(52): Show | 55 | 190 | 0.2895 | -1 | c.719 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1221632 | TG | T | intron_variant | MODIFIER | HG00323.hp1 HG00438.hp2 HG00673.hp1 others(44): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0002a0002c0003others(17): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(21): Show | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0025others(44): Show | 47 | 190 | 0.2474 | -1 | c.719 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1222878 | GC | G | intron_variant | MODIFIER | HG03490.hp2 HG04184.hp1 |
a0004a0006 | a0004c0014a0006c0010 | a0004c0014t0001a0006c0010t0001 | a0004c0014t0001g0054a0006c0010t0001g0012 | 2 | 190 | 0.0105 | -1 | c.719 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1223088 | GC | G | intron_variant | MODIFIER | HG01081.hp2 NA19084.hp2 |
a0001a0002 | a0001c0001a0002c0005 | a0001c0001t0001a0002c0005t0001 | a0001c0001t0001g0039a0002c0005t0001g0020 | 2 | 190 | 0.0105 | -1 | c.719 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1235582 | GA | G | intron_variant | MODIFIER | HG01261.hp1 HG02572.hp2 HG02615.hp2 |
a0003a0009a0018 | a0003c0007a0009c0029a0018c0023 | a0003c0007t0001a0009c0029t0001a0018c0023t0001 | a0003c0007t0001g0184a0009c0029t0001g0152a0018c0023t0001g0048 | 3 | 190 | 0.0158 | -1 | c.720 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1238533 | TG | T | intron_variant | MODIFIER | HG02486.hp2 HG02630.hp2 HG02647.hp1 |
a0003a0006a0011 | a0003c0007a0006c0009a0011c0018 | a0003c0007t0001a0006c0009t0001a0011c0018t0001 | a0003c0007t0001g0108a0006c0009t0001g0049a0011c0018t0001g0045 | 3 | 190 | 0.0158 | -1 | c.849 others(8): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 10/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1244130 | CG | C | intron_variant | MODIFIER | HG00735.hp1 HG01099.hp1 HG01192.hp1 others(18): Show |
a0003a0005a0006others(5): Show | a0003c0007a0003c0008a0005c0006others(6): Show | a0003c0007t0001a0003c0008t0001a0005c0006t0001others(6): Show | a0003c0007t0001g0018a0003c0007t0001g0068a0003c0007t0001g0080others(18): Show | 21 | 190 | 0.1105 | -1 | c.889 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 11/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1244662 | CT | C | intron_variant | MODIFIER | HG00673.hp2 HG01106.hp1 HG01169.hp2 others(53): Show |
a0003a0004a0005others(6): Show | a0003c0007a0003c0008a0004c0004others(11): Show | a0003c0007t0001a0003c0007t0002a0003c0008t0001others(15): Show | a0003c0007t0001g0008a0003c0007t0001g0055a0003c0007t0001g0104others(53): Show | 56 | 190 | 0.2947 | -1 | c.889 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 11/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1255886 | AT | A | intron_variant | MODIFIER | HG00642.hp1 HG00673.hp2 HG01106.hp1 others(51): Show |
a0003a0004a0005others(6): Show | a0003c0007a0003c0008a0004c0004others(11): Show | a0003c0007t0001a0003c0007t0002a0003c0008t0001others(15): Show | a0003c0007t0001g0008a0003c0007t0001g0055a0003c0007t0001g0104others(51): Show | 54 | 190 | 0.2842 | -1 | c.100 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 12/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1256962 | TC | T | intron_variant | MODIFIER | HG00642.hp1 HG00673.hp2 HG01106.hp1 others(54): Show |
a0003a0004a0005others(6): Show | a0003c0007a0003c0008a0004c0004others(11): Show | a0003c0007t0001a0003c0007t0002a0003c0008t0001others(15): Show | a0003c0007t0001g0008a0003c0007t0001g0055a0003c0007t0001g0104others(54): Show | 57 | 190 | 0.3000 | -1 | c.100 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 12/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1261085 | TA | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
a0001a0002a0003others(20): Show | a0001c0001a0001c0002a0002c0003others(33): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(41): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(186): Show | 189 | 190 | 0.9947 | -1 | c.107 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1267747 | TA | T | intron_variant | MODIFIER | HG00642.hp1 HG00673.hp2 HG00735.hp1 others(78): Show |
a0003a0004a0005others(10): Show | a0003c0007a0003c0008a0003c0026others(16): Show | a0003c0007t0001a0003c0007t0002a0003c0008t0001others(21): Show | a0003c0007t0001g0008a0003c0007t0001g0018a0003c0007t0001g0055others(78): Show | 81 | 190 | 0.4263 | -1 | c.128 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1273312 | TC | T | intron_variant | MODIFIER | HG00642.hp1 HG00673.hp2 HG01106.hp1 others(55): Show |
a0003a0004a0005others(5): Show | a0003c0007a0003c0008a0004c0004others(10): Show | a0003c0007t0001a0003c0007t0002a0003c0008t0001others(15): Show | a0003c0007t0001g0008a0003c0007t0001g0055a0003c0007t0001g0104others(55): Show | 58 | 190 | 0.3053 | -1 | c.128 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 14/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1285787 | GT | G | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(77): Show |
a0001a0003a0004others(11): Show | a0001c0001a0001c0002a0003c0007others(19): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(24): Show | a0001c0001t0001g0024a0001c0001t0001g0035a0001c0001t0001g0038others(77): Show | 80 | 190 | 0.4211 | -1 | c.128 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1290317 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(57): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0002a0002c0005others(16): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(18): Show | a0001c0001t0001g0024a0001c0001t0001g0035a0001c0001t0001g0038others(57): Show | 60 | 190 | 0.3158 | -1 | c.128 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1292209 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(85): Show |
a0001a0002a0004others(7): Show | a0001c0001a0001c0002a0002c0003others(14): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(18): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(85): Show | 88 | 190 | 0.4632 | -1 | c.128 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1293157 | CT | C | intron_variant | MODIFIER | HG01256.hp2 HG01257.hp1 HG01517.hp2 others(5): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0005a0003c0007others(5): Show | a0001c0001t0001a0002c0005t0001a0003c0007t0001others(5): Show | a0001c0001t0001g0179a0002c0005t0001g0107a0003c0007t0001g0108others(5): Show | 8 | 190 | 0.0421 | -1 | c.128 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1302540 | TA | T | intron_variant | MODIFIER | HG01169.hp2 HG01516.hp1 HG02015.hp2 others(16): Show |
a0001a0003a0004others(3): Show | a0001c0001a0003c0008a0004c0004others(4): Show | a0001c0001t0001a0003c0008t0001a0004c0004t0001others(6): Show | a0001c0001t0001g0140a0003c0008t0001g0044a0004c0004t0001g0149others(16): Show | 19 | 190 | 0.1000 | -1 | c.128 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1304728 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(122): Show |
a0001a0002a0003others(19): Show | a0001c0001a0001c0002a0002c0003others(31): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(35): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(122): Show | 125 | 190 | 0.6579 | -1 | c.128 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1312215 | GT | G | intron_variant | MODIFIER | HG00735.hp1 HG01099.hp1 HG01257.hp2 others(30): Show |
a0001a0003a0006others(9): Show | a0001c0001a0001c0002a0003c0007others(13): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(15): Show | a0001c0001t0001g0102a0001c0002t0001g0084a0001c0002t0001g0109others(30): Show | 33 | 190 | 0.1737 | -1 | c.137 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1318797 | CT | C | intron_variant | MODIFIER | HG00735.hp1 HG01099.hp1 HG01257.hp2 others(25): Show |
a0001a0003a0006others(9): Show | a0001c0001a0001c0002a0003c0007others(13): Show | a0001c0001t0001a0001c0002t0001a0003c0007t0001others(13): Show | a0001c0001t0001g0102a0001c0002t0001g0109a0003c0007t0001g0018others(25): Show | 28 | 190 | 0.1474 | -1 | c.148 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1320534 | CA | C | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(97): Show |
a0001a0002a0003others(13): Show | a0001c0001a0001c0002a0002c0003others(20): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(25): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(97): Show | 100 | 190 | 0.5263 | -1 | c.148 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1326341 | AT | A | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp2 NA20805.hp1 |
a0002 | a0002c0003a0002c0005 | a0002c0003t0001a0002c0005t0001 | a0002c0003t0001g0052a0002c0003t0001g0098a0002c0005t0001g0168 | 3 | 190 | 0.0158 | -1 | c.148 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |