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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
TNRC6B_chr22_40172925_40340808 | 40217972 | C | CAA | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(125): Show |
a0001a0003a0004others(3): Show | a0001c0001a0001c0005a0001c0013others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(59): Show | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(125): Show |
128 | 308 | 0.4156 | 2 | c.6-2 others(17): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
TNRC6B_chr22_40172925_40340808 | 40218324 | C | CTT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(84): Show |
a0001a0005a0007others(1): Show | a0001c0001a0001c0008a0001c0013others(5): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(41): Show | a0001c0001t0002g0217 a0001c0001t0002g0218 a0001c0001t0002g0226 others(84): Show |
87 | 308 | 0.2825 | 2 | c.6-2 others(17): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
TNRC6B_chr22_40172925_40340808 | 40221761 | C | CCT | intron_variant | MODIFIER | HG00738.hp2 HG01934.hp2 HG02027.hp2 others(10): Show |
a0001 | a0001c0001a0001c0015 | a0001c0001t0001a0001c0001t0017a0001c0001t0024others(7): Show | a0001c0001t0001g0015 a0001c0001t0001g0034 a0001c0001t0001g0037 others(10): Show |
13 | 308 | 0.0422 | 2 | c.6-2 others(17): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | chr22 | TogoVar | |||||||
TNRC6B_chr22_40172925_40340808 | 40222728 | C | CTT | intron_variant | MODIFIER | HG01257.hp2 HG01884.hp1 HG02615.hp1 others(6): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0006 | a0001c0001t0042a0001c0001t0052a0002c0002t0032others(6): Show | a0001c0001t0042g0003 a0001c0001t0052g0002 a0002c0002t0032g0127 others(6): Show |
9 | 308 | 0.0292 | 2 | c.6-2 others(17): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
TNRC6B_chr22_40172925_40340808 | 40227358 | C | CTT | intron_variant | MODIFIER | HG00438.hp2 HG00735.hp1 HG00741.hp1 others(30): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(19): Show | a0001c0001t0002g0218 a0001c0001t0002g0227 a0001c0001t0002g0230 others(30): Show |
33 | 308 | 0.1071 | 2 | c.6-1 others(17): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
TNRC6B_chr22_40172925_40340808 | 40231053 | C | CTA | intron_variant | MODIFIER | HG01109.hp1 HG02647.hp2 HG02723.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0033a0001c0001t0034others(2): Show | a0001c0001t0006g0150 a0001c0001t0033g0146 a0001c0001t0034g0091 others(2): Show |
5 | 308 | 0.0162 | 2 | c.6-1 others(17): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
TNRC6B_chr22_40172925_40340808 | 40242179 | A | AGT | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(111): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0005a0001c0015others(6): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(59): Show | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(111): Show |
114 | 308 | 0.3701 | 2 | c.6-3 others(15): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
TNRC6B_chr22_40172925_40340808 | 40258071 | C | CTT | intron_variant | MODIFIER | HG00735.hp2 HG01261.hp1 HG02135.hp1 others(9): Show |
a0001a0007 | a0001c0001a0007c0018 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(7): Show | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0003g0163 others(9): Show |
12 | 308 | 0.0390 | 2 | c.116 others(19): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
TNRC6B_chr22_40172925_40340808 | 40269887 | C | CAA | intron_variant | MODIFIER | HG01123.hp1 HG02027.hp1 HG02135.hp1 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(7): Show | a0001c0001t0001g0048 a0001c0001t0001g0076 a0001c0001t0001g0077 others(12): Show |
15 | 308 | 0.0487 | 2 | c.280 others(19): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
TNRC6B_chr22_40172925_40340808 | 40288839 | C | CTT | intron_variant | MODIFIER | HG00438.hp1 HG01106.hp2 HG01175.hp1 others(13): Show |
a0001a0004 | a0001c0001a0001c0005a0004c0004 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(8): Show | a0001c0001t0001g0219 a0001c0001t0004g0178 a0001c0001t0004g0188 others(13): Show |
16 | 308 | 0.0520 | 2 | c.370 others(21): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
TNRC6B_chr22_40172925_40340808 | 40293190 | C | CTT | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(114): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0005a0001c0013others(8): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(60): Show | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0015 others(114): Show |
117 | 308 | 0.3799 | 2 | c.370 others(21): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
TNRC6B_chr22_40172925_40340808 | 40296326 | A | ATT | intron_variant | MODIFIER | HG01069.hp1 HG01891.hp1 HG02055.hp1 others(3): Show |
a0001a0012 | a0001c0001a0012c0010 | a0001c0001t0016a0001c0001t0030a0001c0001t0065others(2): Show | a0001c0001t0016g0089 a0001c0001t0030g0220 a0001c0001t0030g0221 others(3): Show |
6 | 308 | 0.0195 | 2 | c.370 others(21): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
TNRC6B_chr22_40172925_40340808 | 40339927 | C | CTT | downstream_gene_variant | MODIFIER | HG00423.hp1 HG00438.hp2 HG01123.hp2 others(39): Show |
a0001a0004 | a0001c0001a0004c0004 | a0001c0001t0001a0001c0001t0007a0001c0001t0011others(18): Show | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0035 others(39): Show |
42 | 308 | 0.1364 | 2 | c.*16 others(15): Show |
TNRC6B | ENSG00000100354.21 | transcript | ENST00000454349.7 | protein_coding | 4120 | chr22 | TogoVar | |||||||
TNRC6C_chr17_77953703_78113822 | 77961157 | C | CTT | intron_variant | MODIFIER | HG00423.hp1 HG02155.hp2 NA18939.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0047 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 others(4): Show |
7 | 276 | 0.0254 | 2 | c.-38 others(19): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
TNRC6C_chr17_77953703_78113822 | 77976931 | G | GAA | intron_variant | MODIFIER | HG00323.hp1 HG01081.hp2 HG01261.hp1 others(21): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0042others(6): Show | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0027 others(21): Show |
24 | 276 | 0.0870 | 2 | c.-38 others(21): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
TNRC6C_chr17_77953703_78113822 | 77977891 | C | CTT | intron_variant | MODIFIER | HG02155.hp1 HG02647.hp1 HG02895.hp2 others(5): Show |
a0001a0002 | a0001c0004a0001c0006a0002c0003 | a0001c0004t0026a0001c0006t0008a0001c0006t0032others(2): Show | a0001c0004t0026g0260 a0001c0006t0008g0251 a0001c0006t0008g0253 others(5): Show |
8 | 276 | 0.0290 | 2 | c.-38 others(21): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
TNRC6C_chr17_77953703_78113822 | 77984828 | G | GCA | intron_variant | MODIFIER | HG00558.hp1 HG01261.hp1 HG01884.hp1 others(26): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0005others(7): Show | a0001c0001t0001a0001c0002t0035a0001c0005t0001others(11): Show | a0001c0001t0001g0032 a0001c0001t0001g0185 a0001c0001t0001g0187 others(25): Show |
29 | 276 | 0.1051 | 2 | c.-37 others(21): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
TNRC6C_chr17_77953703_78113822 | 77986426 | A | AAG | intron_variant | MODIFIER | HG02258.hp1 HG02486.hp1 HG02615.hp1 others(13): Show |
a0001a0002a0009others(1): Show | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0029a0001c0002t0002a0001c0002t0031others(6): Show | a0001c0001t0029g0239 a0001c0002t0002g0196 a0001c0002t0031g0265 others(13): Show |
16 | 276 | 0.0580 | 2 | c.-37 others(21): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
TNRC6C_chr17_77953703_78113822 | 77988376 | T | TAC | intron_variant | MODIFIER | HG02486.hp1 HG02622.hp2 HG02647.hp1 others(8): Show |
a0001a0002 | a0001c0004a0002c0003 | a0001c0004t0006a0001c0004t0024a0002c0003t0010others(1): Show | a0001c0004t0006g0242 a0001c0004t0006g0244 a0001c0004t0006g0246 others(8): Show |
11 | 276 | 0.0399 | 2 | c.-37 others(21): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
TNRC6C_chr17_77953703_78113822 | 78000618 | G | GCC | intron_variant | MODIFIER | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(69): Show |
a0001a0002a0004others(6): Show | a0001c0001a0001c0002a0001c0004others(10): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(22): Show | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(69): Show |
72 | 276 | 0.2609 | 2 | c.-37 others(19): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
TNRC6C_chr17_77953703_78113822 | 78000630 | C | CCA | intron_variant | MODIFIER | HG02486.hp1 HG02622.hp1 HG02622.hp2 others(11): Show |
a0001a0002a0008 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0017a0001c0002t0013a0001c0002t0018others(5): Show | a0001c0001t0017g0266 a0001c0001t0017g0267 a0001c0002t0013g0235 others(11): Show |
14 | 276 | 0.0507 | 2 | c.-37 others(19): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
TNRC6C_chr17_77953703_78113822 | 78029808 | G | GAC | intron_variant | MODIFIER | HG00735.hp2 HG02976.hp2 NA18943.hp1 others(4): Show |
a0001a0004 | a0001c0001a0004c0008 | a0001c0001t0001a0001c0001t0005a0001c0001t0064others(1): Show | a0001c0001t0001g0096 a0001c0001t0001g0219 a0001c0001t0005g0095 others(4): Show |
7 | 276 | 0.0254 | 2 | c.86- others(17): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
TNRC6C_chr17_77953703_78113822 | 78030325 | C | CGT | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(58): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0029others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(12): Show | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(58): Show |
61 | 276 | 0.2210 | 2 | c.86- others(17): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
TNRC6C_chr17_77953703_78113822 | 78045551 | C | CTT | intron_variant | MODIFIER | HG02647.hp1 HG02895.hp2 HG02970.hp2 others(1): Show |
a0002 | a0002c0003 | a0002c0003t0010a0002c0003t0025 | a0002c0003t0010g0240 a0002c0003t0010g0245 a0002c0003t0010g0250 others(1): Show |
4 | 276 | 0.0145 | 2 | c.413 others(19): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
TNRC6C_chr17_77953703_78113822 | 78057825 | T | TTG | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(64): Show |
a0001a0002a0003others(2): Show | a0001c0002a0001c0004a0001c0006others(7): Show | a0001c0002t0013a0001c0002t0018a0001c0004t0006others(21): Show | a0001c0002t0013g0235 a0001c0002t0013g0236 a0001c0002t0013g0238 others(62): Show |
67 | 276 | 0.2428 | 2 | c.301 others(21): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
TNRC6C_chr17_77953703_78113822 | 78063661 | C | CAG | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(40): Show |
a0002a0006a0007 | a0002c0003a0002c0014a0002c0027others(2): Show | a0002c0003t0003a0002c0003t0007a0002c0003t0010others(11): Show | a0002c0003t0003g0002 a0002c0003t0003g0003 a0002c0003t0003g0004 others(38): Show |
43 | 276 | 0.1558 | 2 | c.301 others(21): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
TNRC6C_chr17_77953703_78113822 | 78086328 | T | TAA | intron_variant | MODIFIER | HG00280.hp2 HG00597.hp1 HG00642.hp1 others(18): Show |
a0001a0004a0015 | a0001c0001a0001c0005a0004c0008others(1): Show | a0001c0001t0001a0001c0001t0021a0001c0001t0049others(3): Show | a0001c0001t0001g0039 a0001c0001t0001g0053 a0001c0001t0001g0062 others(18): Show |
21 | 276 | 0.0761 | 2 | c.409 others(19): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
TNRC6C_chr17_77953703_78113822 | 78105634 | A | AGT | 3_prime_UTR_variant | MODIFIER | HG01070.hp2 HG01071.hp2 HG01255.hp1 others(39): Show |
a0001a0002a0007others(1): Show | a0001c0007a0002c0003a0002c0027others(2): Show | a0001c0007t0012a0002c0003t0003a0002c0003t0007others(10): Show | a0001c0007t0012g0268 a0001c0007t0012g0269 a0001c0007t0012g0270 others(37): Show |
42 | 276 | 0.1522 | 2 | c.*80 others(11): Show |
TNRC6C | ENSG00000078687.18 | transcript | ENST00000696270.1 | protein_coding | 23/23 | 805 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
TNR_chr1_175310194_175748595 | 175312619 | T | TCA | downstream_gene_variant | MODIFIER | HG01361.hp2 HG01978.hp2 HG02165.hp1 others(4): Show |
a0001a0003a0005others(1): Show | a0001c0002a0001c0009a0003c0001others(2): Show | a0001c0002t0001a0001c0009t0017a0003c0001t0005others(4): Show | a0001c0002t0001g0117 a0001c0009t0017g0052 a0003c0001t0005g0123 others(4): Show |
7 | 132 | 0.0530 | 2 | c.*10 others(15): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 2574 | chr1 | TogoVar | |||||||
TNR_chr1_175310194_175748595 | 175312621 | T | TCA | downstream_gene_variant | MODIFIER | HG00738.hp2 HG03041.hp1 HG03453.hp2 others(5): Show |
a0001a0002a0007others(1): Show | a0001c0005a0001c0012a0002c0007others(3): Show | a0001c0005t0069a0001c0012t0020a0002c0007t0043others(3): Show | a0001c0005t0069g0069 a0001c0012t0020g0011 a0001c0012t0020g0082 others(5): Show |
8 | 132 | 0.0606 | 2 | c.*10 others(15): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 2572 | chr1 | TogoVar | |||||||
TNR_chr1_175310194_175748595 | 175313585 | A | ATT | downstream_gene_variant | MODIFIER | HG00323.hp2 HG01071.hp1 HG01081.hp1 others(15): Show |
a0001a0002a0003others(2): Show | a0001c0005a0001c0014a0002c0006others(5): Show | a0001c0005t0002a0001c0014t0065a0002c0006t0042others(12): Show | a0001c0005t0002g0102 a0001c0014t0065g0108 a0002c0006t0042g0044 others(15): Show |
18 | 132 | 0.1364 | 2 | c.*97 others(13): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 1608 | chr1 | TogoVar | |||||||
TNR_chr1_175310194_175748595 | 175315812 | A | ATG | 3_prime_UTR_variant | MODIFIER | HG00140.hp2 HG00738.hp1 HG01891.hp1 others(7): Show |
a0001a0002a0010 | a0001c0002a0002c0008a0010c0028 | a0001c0002t0021a0001c0002t0024a0001c0002t0063others(2): Show | a0001c0002t0021g0010 a0001c0002t0021g0056 a0001c0002t0024g0037 others(7): Show |
10 | 132 | 0.0758 | 2 | c.*75 others(13): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 23/23 | 7544 | chr1 | TogoVar | ||||||
TNR_chr1_175310194_175748595 | 175320697 | C | CGT | 3_prime_UTR_variant | MODIFIER | HG02615.hp1 HG02615.hp2 HG02886.hp1 others(2): Show |
a0001a0002 | a0001c0003a0002c0027 | a0001c0003t0008a0002c0027t0050 | a0001c0003t0008g0004 a0001c0003t0008g0015 a0001c0003t0008g0114 others(2): Show |
5 | 132 | 0.0379 | 2 | c.*26 others(13): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 23/23 | 2659 | chr1 | TogoVar | ||||||
TNR_chr1_175310194_175748595 | 175328101 | C | CTA | intron_variant | MODIFIER | HG02559.hp1 HG02630.hp2 HG02895.hp2 others(4): Show |
a0002a0007a0010 | a0002c0008a0007c0039a0010c0028 | a0002c0008t0006a0002c0008t0019a0007c0039t0019others(1): Show | a0002c0008t0006g0009 a0002c0008t0006g0062 a0002c0008t0006g0094 others(4): Show |
7 | 132 | 0.0530 | 2 | c.379 others(21): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 21/22 | chr1 | TogoVar | |||||||
TNR_chr1_175310194_175748595 | 175331069 | C | CCT | intron_variant | MODIFIER | HG03669.hp1 NA20905.hp1 |
a0002a0003 | a0002c0007a0003c0001 | a0002c0007t0011a0003c0001t0049 | a0002c0007t0011g0110 a0003c0001t0049g0022 |
2 | 132 | 0.0152 | 2 | c.363 others(19): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 20/22 | chr1 | TogoVar | |||||||
TNR_chr1_175310194_175748595 | 175331079 | T | TTC | intron_variant | MODIFIER | HG00642.hp2 HG00738.hp2 HG01243.hp2 others(11): Show |
a0001a0002a0003others(2): Show | a0001c0016a0002c0007a0003c0001others(2): Show | a0001c0016t0046a0002c0007t0010a0002c0007t0043others(9): Show | a0001c0016t0046g0100 a0002c0007t0010g0024 a0002c0007t0043g0126 others(11): Show |
14 | 132 | 0.1061 | 2 | c.363 others(19): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 20/22 | chr1 | TogoVar | |||||||
TNR_chr1_175310194_175748595 | 175331081 | C | CCT | intron_variant | MODIFIER | HG01361.hp2 NA18747.hp2 homoSapiens_chm13v2.hp1 |
a0003a0005a0016 | a0003c0001a0005c0011a0016c0037 | a0003c0001t0002a0005c0011t0015a0016c0037t0011 | a0003c0001t0002g0029 a0005c0011t0015g0032 a0016c0037t0011g0104 |
3 | 132 | 0.0227 | 2 | c.363 others(19): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 20/22 | chr1 | TogoVar | |||||||
TNR_chr1_175310194_175748595 | 175331157 | T | TTC | intron_variant | MODIFIER | HG01081.hp1 HG02165.hp2 HG03195.hp2 others(5): Show |
a0002a0003a0004 | a0002c0006a0002c0007a0003c0001others(1): Show | a0002c0006t0010a0002c0006t0058a0002c0007t0010others(4): Show | a0002c0006t0010g0129 a0002c0006t0058g0079 a0002c0007t0010g0024 others(5): Show |
8 | 132 | 0.0606 | 2 | c.363 others(19): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 20/22 | chr1 | TogoVar | |||||||
TNR_chr1_175310194_175748595 | 175353920 | A | ACT | intron_variant | MODIFIER | HG02280.hp1 HG02630.hp1 HG02886.hp2 others(4): Show |
a0001a0013 | a0001c0005a0013c0031 | a0001c0005t0002a0001c0005t0007a0001c0005t0034others(2): Show | a0001c0005t0002g0102 a0001c0005t0007g0043 a0001c0005t0007g0071 others(4): Show |
7 | 132 | 0.0530 | 2 | c.338 others(19): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 18/22 | chr1 | TogoVar | |||||||
TNR_chr1_175310194_175748595 | 175371068 | G | GAA | intron_variant | MODIFIER | HG01070.hp1 HG02055.hp2 HG02559.hp2 others(8): Show |
a0002a0003a0007 | a0002c0004a0002c0006a0002c0026others(3): Show | a0002c0004t0003a0002c0006t0010a0002c0006t0026others(8): Show | a0002c0004t0003g0113 a0002c0006t0010g0129 a0002c0006t0026g0003 others(8): Show |
11 | 132 | 0.0833 | 2 | c.196 others(21): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 9/22 | chr1 | TogoVar | |||||||
TNR_chr1_175310194_175748595 | 175376860 | T | TTA | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp2 HG01891.hp2 others(14): Show |
a0002a0004a0006others(3): Show | a0002c0004a0002c0008a0004c0019others(4): Show | a0002c0004t0003a0002c0008t0006a0002c0008t0019others(5): Show | a0002c0004t0003g0012 a0002c0004t0003g0013 a0002c0004t0003g0014 others(14): Show |
17 | 132 | 0.1288 | 2 | c.196 others(21): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 9/22 | chr1 | TogoVar | |||||||
TNR_chr1_175310194_175748595 | 175402313 | C | CAA | intron_variant | MODIFIER | HG00140.hp1 HG01081.hp2 HG01175.hp1 others(8): Show |
a0001a0003a0004others(2): Show | a0001c0002a0001c0003a0001c0010others(5): Show | a0001c0002t0022a0001c0003t0004a0001c0010t0012others(8): Show | a0001c0002t0022g0053 a0001c0003t0004g0064 a0001c0010t0012g0083 others(8): Show |
11 | 132 | 0.0833 | 2 | c.976 others(17): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 4/22 | chr1 | TogoVar | |||||||
TNR_chr1_175310194_175748595 | 175416116 | T | TTA | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG02055.hp1 others(5): Show |
a0001a0012a0014 | a0001c0002a0001c0014a0012c0036others(1): Show | a0001c0002t0021a0001c0002t0022a0001c0002t0027others(5): Show | a0001c0002t0021g0056 a0001c0002t0022g0053 a0001c0002t0027g0002 others(5): Show |
8 | 132 | 0.0606 | 2 | c.-63 others(19): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 2/22 | chr1 | TogoVar | |||||||
TNR_chr1_175310194_175748595 | 175416129 | T | TAC | intron_variant | MODIFIER | HG01069.hp2 HG02056.hp1 HG02071.hp1 others(10): Show |
a0001a0004 | a0001c0005a0001c0009a0001c0013others(3): Show | a0001c0005t0002a0001c0005t0007a0001c0005t0054others(8): Show | a0001c0005t0002g0102 a0001c0005t0007g0071 a0001c0005t0054g0008 others(10): Show |
13 | 132 | 0.0985 | 2 | c.-63 others(19): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 2/22 | chr1 | TogoVar | |||||||
TNR_chr1_175310194_175748595 | 175416143 | C | CTA | intron_variant | MODIFIER | HG01081.hp2 HG01978.hp2 HG02976.hp2 others(1): Show |
a0001a0005a0006 | a0001c0003a0005c0035a0006c0015 | a0001c0003t0004a0005c0035t0053a0006c0015t0009 | a0001c0003t0004g0068 a0005c0035t0053g0070 a0006c0015t0009g0084 others(1): Show |
4 | 132 | 0.0303 | 2 | c.-63 others(19): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 2/22 | chr1 | TogoVar | |||||||
TNR_chr1_175310194_175748595 | 175426766 | G | GTA | intron_variant | MODIFIER | HG00738.hp1 HG01070.hp1 HG01070.hp2 others(24): Show |
a0001a0002a0003others(3): Show | a0001c0002a0001c0003a0001c0009others(11): Show | a0001c0002t0001a0001c0002t0022a0001c0002t0024others(19): Show | a0001c0002t0001g0038 a0001c0002t0001g0117 a0001c0002t0001g0130 others(24): Show |
27 | 132 | 0.2046 | 2 | c.-63 others(21): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 2/22 | chr1 | TogoVar | |||||||
TNR_chr1_175310194_175748595 | 175431635 | C | CTT | intron_variant | MODIFIER | HG02109.hp1 HG02895.hp1 HG02922.hp2 others(6): Show |
a0001a0003a0007others(1): Show | a0001c0002a0001c0003a0001c0032others(4): Show | a0001c0002t0027a0001c0003t0004a0001c0032t0001others(6): Show | a0001c0002t0027g0002 a0001c0003t0004g0068 a0001c0032t0001g0101 others(6): Show |
9 | 132 | 0.0682 | 2 | c.-63 others(21): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 2/22 | chr1 | TogoVar | |||||||
TNR_chr1_175310194_175748595 | 175431911 | A | ATC | intron_variant | MODIFIER | HG02559.hp2 NA19043.hp1 NA21309.hp2 |
a0001a0002 | a0001c0003a0002c0006 | a0001c0003t0004a0002c0006t0026 | a0001c0003t0004g0065 a0001c0003t0004g0093 a0002c0006t0026g0003 |
3 | 132 | 0.0227 | 2 | c.-63 others(21): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 2/22 | chr1 | TogoVar | |||||||
TNR_chr1_175310194_175748595 | 175461782 | T | TAC | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(103): Show |
a0001a0002a0003others(11): Show | a0001c0002a0001c0003a0001c0005others(33): Show | a0001c0002t0001a0001c0002t0021a0001c0002t0022others(68): Show | a0001c0002t0001g0033 a0001c0002t0001g0039 a0001c0002t0001g0066 others(103): Show |
106 | 132 | 0.8030 | 2 | c.-63 others(21): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 2/22 | chr1 | TogoVar | |||||||
TNR_chr1_175310194_175748595 | 175466623 | G | GAC | intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG02258.hp2 others(7): Show |
a0001a0002a0003others(2): Show | a0001c0002a0001c0003a0001c0010others(5): Show | a0001c0002t0022a0001c0003t0004a0001c0010t0012others(7): Show | a0001c0002t0022g0053 a0001c0003t0004g0065 a0001c0010t0012g0083 others(7): Show |
10 | 132 | 0.0758 | 2 | c.-63 others(21): Show |
TNR | ENSG00000116147.18 | transcript | ENST00000367674.7 | protein_coding | 2/22 | chr1 | TogoVar |