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 | 968142 | GT | G | intron_variant | MODIFIER | HG00140.hp1 HG00642.hp1 HG01081.hp2 others(29): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0002c0003others(10): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(10): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(29): Show | 32 | 190 | 0.1684 | -1 | c.72+ others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 971714 | CT | C | intron_variant | MODIFIER | HG00140.hp1 HG00642.hp1 HG01081.hp2 others(29): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0002c0003others(10): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(10): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(29): Show | 32 | 190 | 0.1684 | -1 | c.72+ others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 984259 | CT | C | intron_variant | MODIFIER | HG00140.hp1 HG00642.hp1 HG01081.hp2 others(37): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0002c0003others(13): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(13): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(37): Show | 40 | 190 | 0.2105 | -1 | c.72+ others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 986739 | GA | G | intron_variant | MODIFIER | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(24): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0002a0002c0003others(13): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(14): Show | a0001c0001t0001g0062a0001c0001t0001g0140a0001c0001t0001g0141others(24): Show | 27 | 190 | 0.1421 | -1 | c.72+ others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 988729 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00735.hp2 others(22): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0002c0003others(9): Show | a0001c0001t0001a0001c0002t0004a0002c0003t0001others(9): Show | a0001c0001t0001g0063a0001c0001t0001g0067a0001c0002t0004g0053others(22): Show | 25 | 190 | 0.1316 | -1 | c.72+ others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 989418 | AT | A | intron_variant | MODIFIER | HG00140.hp1 HG00642.hp1 HG01081.hp2 others(29): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0002c0003others(12): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(12): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(29): Show | 32 | 190 | 0.1684 | -1 | c.72+ others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1002690 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(44): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0002c0003others(14): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0004others(15): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(44): Show | 47 | 190 | 0.2474 | -1 | c.72+ others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1009234 | CA | C | intron_variant | MODIFIER | HG01074.hp1 HG01081.hp1 HG01099.hp2 others(25): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0002a0002c0003others(11): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(12): Show | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(25): Show | 28 | 190 | 0.1474 | -1 | c.72+ others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1009359 | CA | C | intron_variant | MODIFIER | HG02965.hp2 HG03579.hp1 NA18522.hp2 |
a0003a0004a0006 | a0003c0008a0004c0004a0006c0028 | a0003c0008t0001a0004c0004t0001a0006c0028t0001 | a0003c0008t0001g0106a0004c0004t0001g0116a0006c0028t0001g0117 | 3 | 190 | 0.0158 | -1 | c.72+ others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1009421 | CA | C | intron_variant | MODIFIER | HG01074.hp1 HG01081.hp1 HG01099.hp2 others(25): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0002a0002c0003others(11): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(12): Show | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(25): Show | 28 | 190 | 0.1474 | -1 | c.72+ others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1009483 | CA | C | intron_variant | MODIFIER | HG01074.hp1 HG01081.hp1 HG01099.hp2 others(25): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0002a0002c0003others(11): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(12): Show | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(25): Show | 28 | 190 | 0.1474 | -1 | c.72+ others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1011680 | CT | C | intron_variant | MODIFIER | HG00140.hp1 HG00438.hp1 HG00642.hp1 others(58): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0002a0002c0003others(18): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(20): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(58): Show | 61 | 190 | 0.3211 | -1 | c.72+ others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1011800 | TA | T | intron_variant | MODIFIER | HG02965.hp2 HG03579.hp1 NA18522.hp2 |
a0003a0004a0006 | a0003c0008a0004c0004a0006c0028 | a0003c0008t0001a0004c0004t0001a0006c0028t0001 | a0003c0008t0001g0106a0004c0004t0001g0116a0006c0028t0001g0117 | 3 | 190 | 0.0158 | -1 | c.72+ others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1016538 | GC | G | intron_variant | MODIFIER | HG00140.hp2 HG01074.hp1 HG01081.hp1 others(12): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(2): Show | a0001c0001t0001g0038a0001c0001t0001g0058a0001c0001t0001g0140others(12): Show | 15 | 190 | 0.0790 | -1 | c.72+ others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1018730 | CA | C | intron_variant | MODIFIER | HG02071.hp1 HG03831.hp2 NA18942.hp1 others(1): Show |
a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0113a0002c0003t0001g0165a0002c0003t0001g0171others(1): Show | 4 | 190 | 0.0211 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1028738 | CT | C | intron_variant | MODIFIER | HG02895.hp1 HG02965.hp1 HG02965.hp2 others(4): Show |
a0001a0003a0004others(3): Show | a0001c0002a0003c0008a0004c0004others(3): Show | a0001c0002t0001a0003c0008t0001a0004c0004t0001others(3): Show | a0001c0002t0001g0069a0001c0002t0001g0133a0003c0008t0001g0106others(4): Show | 7 | 190 | 0.0368 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1029511 | GA | G | intron_variant | MODIFIER | HG03225.hp1 HG03471.hp1 NA20129.hp1 |
a0001a0004a0005 | a0001c0002a0004c0014a0005c0006 | a0001c0002t0002a0004c0014t0002a0005c0006t0002 | a0001c0002t0002g0002a0004c0014t0002g0001a0005c0006t0002g0003 | 3 | 190 | 0.0158 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1031527 | TA | T | intron_variant | MODIFIER | HG02895.hp1 HG02970.hp1 NA18969.hp2 |
a0014a0015a0022 | a0014c0035a0015c0036a0022c0021 | a0014c0035t0001a0015c0036t0001a0022c0021t0001 | a0014c0035t0001g0071a0015c0036t0001g0070a0022c0021t0001g0111 | 3 | 190 | 0.0158 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1031528 | AT | A | intron_variant | MODIFIER | HG02109.hp1 HG02280.hp2 HG02647.hp1 others(9): Show |
a0001a0002a0003others(5): Show | a0001c0002a0002c0003a0003c0008others(6): Show | a0001c0002t0001a0002c0003t0001a0003c0008t0001others(6): Show | a0001c0002t0001g0069a0001c0002t0001g0186a0002c0003t0001g0171others(9): Show | 12 | 190 | 0.0632 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1036991 | TG | T | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(92): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0002a0002c0003others(24): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(29): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(92): Show | 95 | 190 | 0.5000 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1045029 | GT | G | intron_variant | MODIFIER | HG00438.hp2 HG01109.hp1 HG01516.hp2 others(12): Show |
a0001a0002a0003others(5): Show | a0001c0002a0002c0005a0002c0022others(6): Show | a0001c0002t0001a0001c0002t0004a0002c0005t0001others(7): Show | a0001c0002t0001g0145a0001c0002t0001g0170a0001c0002t0001g0186others(12): Show | 15 | 190 | 0.0790 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1046146 | CA | C | intron_variant | MODIFIER | HG02965.hp1 NA19030.hp1 |
a0001a0002 | a0001c0002a0002c0033 | a0001c0002t0001a0002c0033t0001 | a0001c0002t0001g0133a0002c0033t0001g0119 | 2 | 190 | 0.0105 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1053311 | GT | G | intron_variant | MODIFIER | HG00438.hp2 HG00673.hp1 HG01109.hp1 others(52): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0002a0002c0005others(19): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(22): Show | a0001c0001t0001g0102a0001c0002t0001g0069a0001c0002t0001g0084others(52): Show | 55 | 190 | 0.2895 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1056614 | AG | A | intron_variant | MODIFIER | HG01081.hp1 HG01257.hp2 HG01496.hp2 others(6): Show |
a0001a0002a0003 | a0001c0001a0002c0003a0003c0008 | a0001c0001t0001a0002c0003t0001a0003c0008t0001 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0063others(6): Show | 9 | 190 | 0.0474 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1056940 | GC | G | intron_variant | MODIFIER | HG01099.hp2 HG01175.hp2 HG01261.hp1 others(5): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0003others(3): Show | a0001c0001t0001a0001c0002t0002a0002c0003t0001others(3): Show | a0001c0001t0001g0058a0001c0002t0002g0076a0002c0003t0001g0129others(5): Show | 8 | 190 | 0.0421 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1056976 | GC | G | intron_variant | MODIFIER | HG01175.hp2 HG02071.hp2 |
a0001a0002 | a0001c0002a0002c0003 | a0001c0002t0001a0002c0003t0001 | a0001c0002t0001g0029a0002c0003t0001g0129 | 2 | 190 | 0.0105 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1059361 | CA | C | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(99): Show |
a0001a0002a0003others(13): Show | a0001c0001a0001c0002a0002c0003others(21): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(24): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(99): Show | 102 | 190 | 0.5368 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1061090 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(58): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0002a0002c0003others(15): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(18): Show | a0001c0001t0001g0035a0001c0001t0001g0038a0001c0001t0001g0039others(58): Show | 61 | 190 | 0.3211 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1066717 | AT | A | intron_variant | MODIFIER | HG02280.hp2 HG02647.hp1 HG02886.hp2 others(3): Show |
a0007a0009a0011others(2): Show | a0007c0017a0009c0013a0011c0018others(2): Show | a0007c0017t0001a0009c0013t0001a0011c0018t0001others(2): Show | a0007c0017t0001g0105a0009c0013t0001g0132a0011c0018t0001g0045others(3): Show | 6 | 190 | 0.0316 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1069489 | GA | G | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG01081.hp2 others(26): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0002c0005others(9): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0004others(10): Show | a0001c0001t0001g0173a0001c0002t0001g0017a0001c0002t0001g0087others(26): Show | 29 | 190 | 0.1526 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1071513 | AG | A | intron_variant | MODIFIER | HG00140.hp1 HG01081.hp2 HG01109.hp1 others(17): Show |
a0001a0002a0003others(5): Show | a0001c0002a0002c0005a0002c0022others(6): Show | a0001c0002t0001a0001c0002t0004a0002c0005t0001others(7): Show | a0001c0002t0001g0017a0001c0002t0001g0126a0001c0002t0001g0145others(17): Show | 20 | 190 | 0.1053 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1071649 | AT | A | intron_variant | MODIFIER | HG01257.hp2 HG02486.hp1 |
a0003 | a0003c0007a0003c0008 | a0003c0007t0001a0003c0008t0001 | a0003c0007t0001g0008a0003c0008t0001g0060 | 2 | 190 | 0.0105 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1071650 | TA | T | intron_variant | MODIFIER | HG00140.hp1 HG01081.hp2 HG01106.hp1 others(14): Show |
a0001a0002a0003others(3): Show | a0001c0002a0002c0005a0002c0022others(4): Show | a0001c0002t0001a0001c0002t0004a0002c0005t0001others(5): Show | a0001c0002t0001g0017a0001c0002t0001g0126a0001c0002t0001g0145others(14): Show | 17 | 190 | 0.0895 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1072348 | TC | T | intron_variant | MODIFIER | HG01192.hp2 HG01346.hp1 HG01975.hp2 others(17): Show |
a0001a0002a0003others(4): Show | a0001c0002a0002c0005a0003c0007others(4): Show | a0001c0002t0001a0002c0005t0001a0003c0007t0001others(4): Show | a0001c0002t0001g0007a0001c0002t0001g0010a0001c0002t0001g0022others(17): Show | 20 | 190 | 0.1053 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1072349 | CT | C | intron_variant | MODIFIER | HG00323.hp2 HG00735.hp2 HG01074.hp2 others(14): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0003a0002c0033others(4): Show | a0001c0001t0001a0002c0003t0001a0002c0033t0001others(4): Show | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0063others(14): Show | 17 | 190 | 0.0895 | -1 | c.73- others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1075581 | AG | A | intron_variant | MODIFIER | HG02145.hp1 HG02258.hp2 |
a0004 | a0004c0004 | a0004c0004t0001 | a0004c0004t0001g0150a0004c0004t0001g0151 | 2 | 190 | 0.0105 | -1 | c.73- others(8): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1083184 | AT | A | intron_variant | MODIFIER | HG00323.hp2 HG00735.hp2 HG01074.hp2 others(37): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0002a0002c0003others(13): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(14): Show | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0063others(37): Show | 40 | 190 | 0.2105 | -1 | c.73- others(7): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1083260 | AC | A | intron_variant | MODIFIER | HG01109.hp2 HG02615.hp1 HG03453.hp1 others(2): Show |
a0002a0003a0005 | a0002c0005a0002c0033a0003c0007others(1): Show | a0002c0005t0001a0002c0033t0001a0003c0007t0001others(2): Show | a0002c0005t0001g0101a0002c0033t0001g0119a0003c0007t0001g0104others(2): Show | 5 | 190 | 0.0263 | -1 | c.73- others(7): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1090096 | CA | C | intron_variant | MODIFIER | HG02145.hp2 HG02451.hp1 HG03225.hp1 others(4): Show |
a0001a0004a0005 | a0001c0002a0004c0014a0005c0006 | a0001c0002t0001a0001c0002t0002a0004c0014t0002others(1): Show | a0001c0002t0001g0041a0001c0002t0001g0069a0001c0002t0001g0109others(4): Show | 7 | 190 | 0.0368 | -1 | c.210 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 2/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1092252 | AG | A | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(63): Show |
a0001a0002a0003others(11): Show | a0001c0001a0002c0003a0003c0007others(14): Show | a0001c0001t0001a0001c0001t0003a0002c0003t0001others(15): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0024others(63): Show | 66 | 190 | 0.3474 | -1 | c.211 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 2/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1094098 | CA | C | intron_variant | MODIFIER | HG02145.hp2 HG02451.hp1 HG03225.hp1 others(5): Show |
a0001a0002a0004others(1): Show | a0001c0002a0002c0033a0004c0014others(1): Show | a0001c0002t0001a0001c0002t0002a0002c0033t0001others(2): Show | a0001c0002t0001g0041a0001c0002t0001g0069a0001c0002t0001g0109others(5): Show | 8 | 190 | 0.0421 | -1 | c.211 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1105277 | AG | A | intron_variant | MODIFIER | HG00323.hp2 HG00735.hp2 HG01074.hp2 others(31): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0002c0003others(11): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(14): Show | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0063others(31): Show | 34 | 190 | 0.1790 | -1 | c.325 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1106399 | CG | C | intron_variant | MODIFIER | HG01106.hp2 HG01496.hp1 HG02132.hp2 others(2): Show |
a0002a0004a0006 | a0002c0003a0004c0004a0006c0009 | a0002c0003t0001a0004c0004t0001a0006c0009t0001 | a0002c0003t0001g0026a0002c0003t0001g0091a0002c0003t0001g0148others(2): Show | 5 | 190 | 0.0263 | -1 | c.325 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1106555 | CG | C | intron_variant | MODIFIER | HG01106.hp2 HG01496.hp1 HG02132.hp2 others(2): Show |
a0002a0004a0006 | a0002c0003a0004c0004a0006c0009 | a0002c0003t0001a0004c0004t0001a0006c0009t0001 | a0002c0003t0001g0026a0002c0003t0001g0091a0002c0003t0001g0148others(2): Show | 5 | 190 | 0.0263 | -1 | c.325 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1106659 | CG | C | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(41): Show |
a0001a0002a0003others(7): Show | a0001c0001a0002c0003a0002c0005others(12): Show | a0001c0001t0001a0001c0001t0003a0002c0003t0001others(13): Show | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0025others(41): Show | 44 | 190 | 0.2316 | -1 | c.325 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1107075 | CG | C | intron_variant | MODIFIER | HG01109.hp2 HG02486.hp1 HG02615.hp1 |
a0002a0003 | a0002c0005a0003c0007 | a0002c0005t0001a0003c0007t0001 | a0002c0005t0001g0101a0003c0007t0001g0008a0003c0007t0001g0104 | 3 | 190 | 0.0158 | -1 | c.325 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1107179 | CG | C | intron_variant | MODIFIER | HG01891.hp2 HG02559.hp2 HG02922.hp2 others(3): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0033a0003c0008others(3): Show | a0001c0001t0001a0002c0033t0001a0003c0008t0001others(3): Show | a0001c0001t0001g0102a0002c0033t0001g0119a0003c0008t0001g0100others(3): Show | 6 | 190 | 0.0316 | -1 | c.325 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1107231 | CG | C | intron_variant | MODIFIER | HG01109.hp2 HG02486.hp1 HG02615.hp1 |
a0002a0003 | a0002c0005a0003c0007 | a0002c0005t0001a0003c0007t0001 | a0002c0005t0001g0101a0003c0007t0001g0008a0003c0007t0001g0104 | 3 | 190 | 0.0158 | -1 | c.325 others(9): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1119577 | AT | A | intron_variant | MODIFIER | HG01891.hp2 HG02559.hp2 HG02922.hp2 others(4): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0033a0003c0007others(3): Show | a0001c0001t0001a0002c0033t0001a0003c0007t0001others(3): Show | a0001c0001t0001g0102a0002c0033t0001g0119a0003c0007t0001g0080others(4): Show | 7 | 190 | 0.0368 | -1 | c.326 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 4/16 | chr2 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1122722 | CA | C | intron_variant | MODIFIER | HG01109.hp2 HG02486.hp1 HG02615.hp1 others(4): Show |
a0002a0003a0007 | a0002c0005a0002c0033a0003c0007others(1): Show | a0002c0005t0001a0002c0033t0001a0003c0007t0001others(2): Show | a0002c0005t0001g0101a0002c0033t0001g0119a0003c0007t0001g0008others(4): Show | 7 | 190 | 0.0368 | -1 | c.326 others(10): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |