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 | 1335181 | GT | G | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(63): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0002a0002c0003others(15): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(18): Show | a0001c0001t0001g0102a0001c0002t0001g0084a0001c0002t0001g0109others(63): Show | 66 | 190 | 0.3474 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1341846 | CT | C | intron_variant | MODIFIER | HG01169.hp1 HG02145.hp2 HG02922.hp2 others(3): Show |
a0001a0002a0006others(1): Show | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(2): Show | a0001c0001t0001g0102a0001c0002t0001g0109a0002c0003t0001g0021others(3): Show | 6 | 190 | 0.0316 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1342362 | TC | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(52): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0002a0002c0003others(17): Show | a0001c0001t0001a0001c0002t0002a0002c0003t0001others(18): Show | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0178others(52): Show | 55 | 190 | 0.2895 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1342585 | CT | C | intron_variant | MODIFIER | HG00140.hp2 HG00673.hp1 HG00735.hp1 others(18): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0002c0003others(7): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(7): Show | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0123others(18): Show | 21 | 190 | 0.1105 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1342589 | TC | T | intron_variant | MODIFIER | HG01891.hp1 HG01975.hp1 HG02145.hp2 others(8): Show |
a0001a0002a0003others(5): Show | a0001c0002a0002c0003a0003c0007others(5): Show | a0001c0002t0001a0001c0002t0002a0002c0003t0001others(6): Show | a0001c0002t0001g0109a0001c0002t0002g0002a0002c0003t0001g0030others(8): Show | 11 | 190 | 0.0579 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1342699 | CT | C | intron_variant | MODIFIER | HG01256.hp1 HG01261.hp2 HG02148.hp1 others(10): Show |
a0001a0002a0003others(5): Show | a0001c0001a0002c0033a0003c0008others(5): Show | a0001c0001t0001a0002c0033t0001a0003c0008t0001others(5): Show | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0178others(10): Show | 13 | 190 | 0.0684 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1342703 | TC | T | intron_variant | MODIFIER | HG01346.hp2 HG02132.hp1 HG02145.hp2 others(17): Show |
a0001a0003a0004others(5): Show | a0001c0001a0001c0002a0003c0007others(7): Show | a0001c0001t0001a0001c0002t0001a0003c0007t0001others(7): Show | a0001c0001t0001g0102a0001c0002t0001g0031a0001c0002t0001g0069others(17): Show | 20 | 190 | 0.1053 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1342813 | CT | C | intron_variant | MODIFIER | HG01169.hp2 HG01346.hp2 HG02132.hp1 others(7): Show |
a0001a0003a0004others(2): Show | a0001c0002a0003c0007a0004c0004others(2): Show | a0001c0002t0001a0003c0007t0001a0004c0004t0001others(4): Show | a0001c0002t0001g0031a0003c0007t0001g0018a0004c0004t0001g0149others(7): Show | 10 | 190 | 0.0526 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1342817 | TC | T | intron_variant | MODIFIER | HG00438.hp1 HG01081.hp2 HG01975.hp1 others(26): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0002a0002c0003others(13): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(14): Show | a0001c0001t0001g0102a0001c0002t0001g0069a0001c0002t0002g0076others(26): Show | 29 | 190 | 0.1526 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1342927 | CT | C | intron_variant | MODIFIER | HG01346.hp2 HG02145.hp1 HG02258.hp2 others(5): Show |
a0001a0003a0004others(3): Show | a0001c0002a0003c0007a0004c0004others(4): Show | a0001c0002t0001a0003c0007t0001a0004c0004t0001others(4): Show | a0001c0002t0001g0084a0003c0007t0001g0018a0004c0004t0001g0150others(5): Show | 8 | 190 | 0.0421 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1342931 | TC | T | intron_variant | MODIFIER | HG01256.hp1 HG01261.hp2 HG02071.hp2 others(21): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0002c0005others(9): Show | a0001c0001t0001a0001c0002t0001a0002c0005t0001others(10): Show | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0102others(21): Show | 24 | 190 | 0.1263 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1343041 | CT | C | intron_variant | MODIFIER | HG00438.hp2 HG00735.hp1 HG01257.hp2 others(12): Show |
a0001a0003a0004others(6): Show | a0001c0002a0003c0007a0003c0008others(8): Show | a0001c0002t0001a0003c0007t0001a0003c0008t0001others(8): Show | a0001c0002t0001g0029a0001c0002t0001g0126a0001c0002t0001g0170others(12): Show | 15 | 190 | 0.0790 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1343045 | TC | T | intron_variant | MODIFIER | HG00323.hp2 HG00642.hp1 HG00673.hp2 others(28): Show |
a0001a0002a0003others(6): Show | a0001c0002a0002c0003a0002c0005others(11): Show | a0001c0002t0001a0001c0002t0002a0002c0003t0001others(13): Show | a0001c0002t0001g0084a0001c0002t0002g0076a0002c0003t0001g0026others(28): Show | 31 | 190 | 0.1632 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1343155 | CT | C | intron_variant | MODIFIER | HG01257.hp2 HG03710.hp1 NA18990.hp2 |
a0003a0008 | a0003c0007a0003c0008a0008c0011 | a0003c0007t0001a0003c0008t0001a0008c0011t0001 | a0003c0007t0001g0080a0003c0008t0001g0060a0008c0011t0001g0004 | 3 | 190 | 0.0158 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1343159 | TC | T | intron_variant | MODIFIER | HG00323.hp2 HG00642.hp1 HG00673.hp2 others(32): Show |
a0002a0003a0004others(6): Show | a0002c0003a0002c0005a0003c0008others(12): Show | a0002c0003t0001a0002c0005t0001a0003c0008t0001others(15): Show | a0002c0003t0001g0051a0002c0003t0001g0064a0002c0003t0001g0098others(32): Show | 35 | 190 | 0.1842 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1343382 | CT | C | intron_variant | MODIFIER | HG00735.hp1 HG02486.hp2 HG03710.hp1 |
a0003 | a0003c0007a0003c0008 | a0003c0007t0001a0003c0008t0001 | a0003c0007t0001g0080a0003c0007t0001g0108a0003c0008t0001g0095 | 3 | 190 | 0.0158 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1343386 | TC | T | intron_variant | MODIFIER | HG00099.hp1 HG00438.hp1 HG01081.hp2 others(32): Show |
a0001a0002a0003others(9): Show | a0001c0002a0002c0003a0002c0005others(13): Show | a0001c0002t0002a0002c0003t0001a0002c0005t0001others(15): Show | a0001c0002t0002g0002a0001c0002t0002g0076a0002c0003t0001g0030others(32): Show | 35 | 190 | 0.1842 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1343496 | CT | C | intron_variant | MODIFIER | HG00735.hp1 HG01257.hp2 HG02486.hp2 others(1): Show |
a0003 | a0003c0007a0003c0008 | a0003c0007t0001a0003c0008t0001 | a0003c0007t0001g0080a0003c0007t0001g0108a0003c0008t0001g0060others(1): Show | 4 | 190 | 0.0211 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1343500 | TC | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(46): Show |
a0001a0002a0003others(8): Show | a0001c0002a0002c0003a0002c0005others(15): Show | a0001c0002t0002a0002c0003t0001a0002c0005t0001others(17): Show | a0001c0002t0002g0002a0002c0003t0001g0030a0002c0003t0001g0051others(46): Show | 49 | 190 | 0.2579 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1344062 | CT | C | intron_variant | MODIFIER | HG00642.hp2 HG01099.hp1 HG01257.hp1 others(7): Show |
a0001a0003a0006others(2): Show | a0001c0001a0001c0002a0003c0007others(3): Show | a0001c0001t0001a0001c0002t0001a0003c0007t0001others(3): Show | a0001c0001t0001g0024a0001c0001t0001g0078a0001c0001t0001g0179others(7): Show | 10 | 190 | 0.0526 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1344066 | TC | T | intron_variant | MODIFIER | HG00438.hp1 HG01081.hp2 HG01496.hp1 others(22): Show |
a0001a0002a0003others(5): Show | a0001c0002a0002c0003a0002c0005others(8): Show | a0001c0002t0001a0002c0003t0001a0002c0005t0001others(9): Show | a0001c0002t0001g0031a0002c0003t0001g0026a0002c0003t0001g0030others(22): Show | 25 | 190 | 0.1316 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1344741 | CT | C | intron_variant | MODIFIER | HG00735.hp1 HG01099.hp1 HG01256.hp1 others(14): Show |
a0001a0002a0003others(6): Show | a0001c0001a0002c0003a0003c0007others(8): Show | a0001c0001t0001a0002c0003t0001a0003c0007t0001others(8): Show | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0136others(14): Show | 17 | 190 | 0.0895 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1344745 | TC | T | intron_variant | MODIFIER | HG00438.hp1 HG02015.hp1 HG02071.hp1 others(15): Show |
a0002a0003a0004others(3): Show | a0002c0003a0002c0005a0002c0033others(8): Show | a0002c0003t0001a0002c0005t0001a0002c0033t0001others(9): Show | a0002c0003t0001g0093a0002c0003t0001g0158a0002c0003t0001g0174others(15): Show | 18 | 190 | 0.0947 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1344968 | CT | C | intron_variant | MODIFIER | HG00735.hp1 HG01099.hp1 HG01256.hp1 others(15): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0002c0003others(8): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(8): Show | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0002t0001g0112others(15): Show | 18 | 190 | 0.0947 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1344972 | TC | T | intron_variant | MODIFIER | HG00099.hp1 HG00438.hp1 HG02109.hp2 others(15): Show |
a0001a0002a0003others(6): Show | a0001c0002a0002c0003a0003c0007others(7): Show | a0001c0002t0001a0001c0002t0002a0002c0003t0001others(10): Show | a0001c0002t0001g0084a0001c0002t0002g0002a0002c0003t0001g0092others(15): Show | 18 | 190 | 0.0947 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1345195 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG00673.hp1 HG01099.hp2 others(32): Show |
a0001a0003a0006others(3): Show | a0001c0001a0001c0002a0003c0007others(6): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(8): Show | a0001c0001t0001g0035a0001c0001t0001g0039a0001c0001t0001g0058others(32): Show | 35 | 190 | 0.1842 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1345199 | TC | T | intron_variant | MODIFIER | HG00438.hp1 HG00642.hp1 HG02109.hp2 others(9): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0002c0003others(6): Show | a0001c0001t0001a0001c0002t0002a0002c0003t0001others(8): Show | a0001c0001t0001g0136a0001c0002t0002g0002a0002c0003t0001g0093others(9): Show | 12 | 190 | 0.0632 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1345422 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG00673.hp1 HG01099.hp1 others(47): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0002a0002c0003others(12): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(14): Show | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0035others(47): Show | 50 | 190 | 0.2632 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1345426 | TC | T | intron_variant | MODIFIER | HG00140.hp1 HG00642.hp2 HG01106.hp2 others(35): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0002c0003others(13): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(17): Show | a0001c0001t0001g0024a0001c0001t0001g0038a0001c0001t0001g0078others(35): Show | 38 | 190 | 0.2000 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1345536 | CT | C | intron_variant | MODIFIER | HG00140.hp1 HG02683.hp1 HG02717.hp2 others(3): Show |
a0001a0003a0010others(1): Show | a0001c0001a0001c0002a0003c0008others(2): Show | a0001c0001t0001a0001c0002t0001a0003c0008t0001others(2): Show | a0001c0001t0001g0038a0001c0002t0001g0017a0003c0008t0001g0013others(3): Show | 6 | 190 | 0.0316 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1345540 | TC | T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(95): Show |
a0001a0002a0003others(16): Show | a0001c0001a0001c0002a0002c0003others(22): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(24): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(95): Show | 98 | 190 | 0.5158 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1345993 | TC | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(40): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0002a0002c0003others(16): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(20): Show | a0001c0001t0001g0015a0001c0001t0001g0057a0001c0001t0001g0062others(40): Show | 43 | 190 | 0.2263 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1346107 | TC | T | intron_variant | MODIFIER | HG00438.hp2 HG00735.hp1 HG01192.hp1 others(14): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0002c0005others(7): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(9): Show | a0001c0001t0001g0038a0001c0001t0001g0062a0001c0001t0001g0140others(14): Show | 17 | 190 | 0.0895 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1346217 | CT | C | intron_variant | MODIFIER | HG00735.hp1 HG01169.hp2 HG02280.hp2 others(5): Show |
a0001a0003a0005others(2): Show | a0001c0002a0003c0008a0005c0006others(2): Show | a0001c0002t0002a0003c0008t0001a0005c0006t0001others(2): Show | a0001c0002t0002g0002a0003c0008t0001g0095a0005c0006t0001g0081others(5): Show | 8 | 190 | 0.0421 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1346221 | TC | T | intron_variant | MODIFIER | HG00642.hp1 HG00642.hp2 HG01099.hp1 others(56): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0002a0002c0003others(21): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(23): Show | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0025others(56): Show | 59 | 190 | 0.3105 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1347090 | GA | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(146): Show |
a0001a0002a0003others(16): Show | a0001c0001a0001c0002a0002c0003others(26): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(33): Show | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0025others(146): Show | 149 | 190 | 0.7842 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1347972 | CT | C | intron_variant | MODIFIER | HG01517.hp1 HG01975.hp2 HG03540.hp2 others(2): Show |
a0001a0003a0004others(1): Show | a0001c0002a0003c0008a0004c0004others(1): Show | a0001c0002t0001a0003c0008t0001a0004c0004t0001others(1): Show | a0001c0002t0001g0007a0001c0002t0001g0084a0003c0008t0001g0190others(2): Show | 5 | 190 | 0.0263 | -1 | c.148 others(11): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1360057 | GA | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
a0001a0002a0003others(15): Show | a0001c0001a0001c0002a0002c0003others(24): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(28): Show | a0001c0001t0001g0016a0001c0001t0001g0024a0001c0001t0001g0025others(136): Show | 139 | 190 | 0.7316 | -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 | 1364146 | AT | A | intron_variant | MODIFIER | HG02280.hp2 HG02615.hp2 HG03471.hp2 others(4): Show |
a0001a0003a0006others(2): Show | a0001c0002a0003c0007a0003c0026others(3): Show | a0001c0002t0001a0001c0002t0002a0003c0007t0001others(4): Show | a0001c0002t0001g0069a0001c0002t0002g0002a0003c0007t0001g0068others(4): Show | 7 | 190 | 0.0368 | -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 | 1365087 | GT | G | intron_variant | MODIFIER | HG02109.hp2 HG02451.hp1 HG02451.hp2 others(11): Show |
a0001a0003a0004others(3): Show | a0001c0001a0001c0002a0003c0007others(6): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(9): Show | a0001c0001t0001g0136a0001c0002t0001g0084a0001c0002t0002g0076others(11): Show | 14 | 190 | 0.0737 | -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 | 1368251 | GA | G | downstream_gene_variant | MODIFIER | HG02109.hp2 HG02280.hp2 HG02451.hp1 others(21): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0002c0033others(12): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(15): Show | a0001c0001t0001g0136a0001c0002t0001g0069a0001c0002t0001g0084others(21): Show | 24 | 190 | 0.1263 | -1 | c.*77 others(5): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 639 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1368662 | CA | C | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00438.hp2 HG00642.hp2 others(58): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0002a0002c0003others(11): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(16): Show | a0001c0001t0001g0024a0001c0001t0001g0035a0001c0001t0001g0039others(58): Show | 61 | 190 | 0.3211 | -1 | c.*11 others(6): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1050 | chr2 | TogoVar | |||||||
SNTN_chr3_63647675_63670212 | 63654858 | TA | T | intron_variant | MODIFIER | HG00323.hp1 HG00438.hp2 HG00621.hp2 others(74): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(4): Show | a0001c0001t0001g0087a0001c0001t0003g0003a0001c0001t0003g0011others(13): Show | 77 | 450 | 0.1711 | -1 | c.145 others(7): Show |
SNTN | ENSG00000188817.8 | transcript | ENST00000343837.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
SNTN_chr3_63647675_63670212 | 63655721 | TA | T | intron_variant | MODIFIER | HG00642.hp1 HG00735.hp2 HG01070.hp2 others(21): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0009 | a0001c0001t0001g0084a0001c0001t0006g0009a0001c0001t0006g0012others(8): Show | 24 | 450 | 0.0533 | -1 | c.145 others(8): Show |
SNTN | ENSG00000188817.8 | transcript | ENST00000343837.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
SNU13_chr22_41668933_41693867 | 41671454 | CA | C | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(106): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(43): Show | 109 | 376 | 0.2899 | -1 | c.*34 others(6): Show |
SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2478 | chr22 | TogoVar | |||||||
SNU13_chr22_41668933_41693867 | 41675744 | CT | C | intron_variant | MODIFIER | HG00639.hp2 HG01243.hp1 HG01496.hp2 others(19): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(2): Show | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0024others(7): Show | 22 | 376 | 0.0585 | -1 | c.125 others(8): Show |
SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | TogoVar | |||||||
SNU13_chr22_41668933_41693867 | 41676531 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0012others(69): Show | 228 | 376 | 0.6064 | -1 | c.125 others(9): Show |
SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 2/2 | chr22 | TogoVar | |||||||
SNU13_chr22_41668933_41693867 | 41681990 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(102): Show | 303 | 376 | 0.8059 | -1 | c.4-1 others(7): Show |
SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | TogoVar | |||||||
SNU13_chr22_41668933_41693867 | 41685968 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(89): Show | 275 | 376 | 0.7314 | -1 | c.3+2 others(7): Show |
SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | TogoVar | |||||||
SNU13_chr22_41668933_41693867 | 41686304 | CT | C | intron_variant | MODIFIER | HG00733.hp2 HG01167.hp1 HG01169.hp1 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0012a0001c0001t0001g0034a0001c0001t0001g0049others(7): Show | 15 | 376 | 0.0399 | -1 | c.3+2 others(7): Show |
SNU13 | ENSG00000100138.15 | transcript | ENST00000401959.6 | protein_coding | 1/2 | chr22 | TogoVar |