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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CACNA1B_chr9_137872782_138129619 | 138018008 | TCAGGTGC others(511): Show |
T | intron_variant | MODIFIER | HG01258.hp2 HG01943.hp2 HG02040.hp1 others(6): Show |
a0002a0003a0011 | a0002c0001a0002c0004a0003c0006others(1): Show | a0002c0001t0001a0002c0001t0002a0002c0001t0003others(3): Show | a0002c0001t0001g0234a0002c0001t0002g0055a0002c0001t0002g0188others(6): Show | 9 | 248 | 0.0363 | -518 | c.226 others(19): Show |
CACNA1B | ENSG00000148408.14 | transcript | ENST00000371372.6 | protein_coding | 18/46 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
CCDC77_chr12_396644_447642 | 419855 | TTCCATTA others(511): Show |
T | intron_variant | MODIFIER | homoSapiens_chm13v2.hp1 | a0004 | a0004c0004 | a0004c0004t0001 | a0004c0004t0001g0187 | 1 | 432 | 0.0023 | -518 | c.413 others(17): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
DNAH17_chr17_78418697_78582396 | 78540766 | GGATGGGT others(511): Show |
G | intron_variant | MODIFIER | HG01123.hp2 HG03225.hp2 |
a0115a0133 | a0115c0222a0133c0202 | a0115c0222t0001a0133c0202t0002 | a0115c0222t0001g0128a0133c0202t0002g0119 | 2 | 252 | 0.0079 | -518 | c.253 others(18): Show |
DNAH17 | ENSG00000187775.17 | transcript | ENST00000389840.7 | protein_coding | 17/80 | chr17 | TogoVar | ||||||
GRIN1_chr9_137134154_137173756 | 137144731 | TGTGGGGA others(511): Show |
T | intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0039 | 1 | 298 | 0.0034 | -518 | c.394 others(15): Show |
GRIN1 | ENSG00000176884.17 | transcript | ENST00000371561.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
JAKMIP3_chr10_132060946_132189858 | 132160925 | TCTCTTCC others(511): Show |
T | intron_variant | MODIFIER | HG02647.hp1 | a0001 | a0001c0042 | a0001c0042t0023 | a0001c0042t0023g0126 | 1 | 158 | 0.0063 | -518 | c.222 others(19): Show |
JAKMIP3 | ENSG00000188385.13 | transcript | ENST00000684848.1 | protein_coding | 19/23 | chr10 | TogoVar | ||||||
RASA3_chr13_113972783_114137623 | 114005853 | CCTCCTGC others(511): Show |
C | intron_variant | MODIFIER | HG02257.hp1 HG02257.hp2 HG02258.hp1 |
a0002 | a0002c0004 | a0002c0004t0004a0002c0004t0009 | a0002c0004t0004g0001a0002c0004t0004g0029a0002c0004t0009g0010 | 3 | 67 | 0.0448 | -518 | c.174 others(19): Show |
RASA3 | ENSG00000185989.11 | transcript | ENST00000334062.8 | protein_coding | 18/23 | chr13 | TogoVar | ||||||
RCOR1_chr14_102587649_102735561 | 102676516 | CACCTCCC others(511): Show |
C | intron_variant | MODIFIER | HG03471.hp1 NA18522.hp1 NA20129.hp1 |
a0001 | a0001c0001 | a0001c0001t0012a0001c0001t0038 | a0001c0001t0012g0152a0001c0001t0012g0153a0001c0001t0038g0155 | 3 | 292 | 0.0103 | -518 | c.362 others(17): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
SKI_chr1_2223319_2315213 | 2281065 | CGATCTTC others(511): Show |
C | intron_variant | MODIFIER | NA18964.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0280 | 1 | 330 | 0.0030 | -518 | c.970 others(19): Show |
SKI | ENSG00000157933.11 | transcript | ENST00000378536.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
SLC7A1_chr13_29504414_29600688 | 29558640 | AGAATGTG others(511): Show |
A | intron_variant | MODIFIER | NA18946.hp2 NA18953.hp1 |
a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0142a0001c0002t0004g0143 | 2 | 330 | 0.0061 | -518 | c.-11 others(19): Show |
SLC7A1 | ENSG00000139514.13 | transcript | ENST00000380752.10 | protein_coding | 1/12 | chr13 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1012995 | TGGGCAGA others(511): Show |
T | intron_variant | MODIFIER | HG01261.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0016 | 1 | 190 | 0.0053 | -518 | c.72+ others(17): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
SNTG2_chr2_945849_1372613 | 1013203 | TAGAGGGA others(511): Show |
T | intron_variant | MODIFIER | HG01517.hp1 HG02148.hp1 HG03831.hp1 others(1): Show |
a0001a0002a0003 | a0001c0001a0002c0003a0003c0008 | a0001c0001t0001a0002c0003t0001a0003c0008t0001 | a0001c0001t0001g0038a0001c0001t0001g0178a0002c0003t0001g0154others(1): Show | 4 | 190 | 0.0211 | -518 | c.72+ others(17): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
SNTG2_chr2_945849_1372613 | 1013772 | AGGGCAGA others(511): Show |
A | intron_variant | MODIFIER | HG03486.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0069 | 1 | 190 | 0.0053 | -518 | c.72+ others(17): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
SNTG2_chr2_945849_1372613 | 1107841 | CACGTGCT others(511): Show |
C | intron_variant | MODIFIER | HG03490.hp2 HG04184.hp2 |
a0001a0004 | a0001c0002a0004c0014 | a0001c0002t0001a0004c0014t0001 | a0001c0002t0001g0137a0004c0014t0001g0054 | 2 | 190 | 0.0105 | -518 | c.325 others(17): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
TFPI_chr2_187459230_187559435 | 187556763 | GGAGGTGG others(511): Show |
G | upstream_gene_variant | MODIFIER | HG03831.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0260 | 1 | 344 | 0.0029 | -518 | c.-30 others(11): Show |
TFPI | ENSG00000003436.16 | transcript | ENST00000233156.9 | protein_coding | 2329 | chr2 | TogoVar | ||||||
USP40_chr2_233470526_233571782 | 233567482 | CTATATAA others(511): Show |
C | upstream_gene_variant | MODIFIER | HG02965.hp2 HG03130.hp2 HG03453.hp1 |
a0002 | a0002c0008 | a0002c0008t0009 | a0002c0008t0009g0119a0002c0008t0009g0120a0002c0008t0009g0123 | 3 | 324 | 0.0093 | -518 | c.-13 others(10): Show |
USP40 | ENSG00000085982.16 | transcript | ENST00000678225.2 | protein_coding | 701 | chr2 | TogoVar | ||||||
ATP11A_chr13_112685038_112892168 | 112766866 | AGGGTGTG others(510): Show |
A | intron_variant | MODIFIER | NA18971.hp2 NA19007.hp1 |
a0001 | a0001c0002 | a0001c0002t0012 | a0001c0002t0012g0191a0001c0002t0012g0252 | 2 | 254 | 0.0079 | -517 | c.40- others(17): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
B3GNTL1_chr17_82937149_83056770 | 83022378 | GCCCACCT others(510): Show |
G | intron_variant | MODIFIER | HG00597.hp1 HG00609.hp1 NA18964.hp1 others(3): Show |
a0001a0002 | a0001c0004a0001c0006a0002c0022 | a0001c0004t0001a0001c0006t0008a0001c0006t0023others(1): Show | a0001c0004t0001g0025a0001c0004t0001g0041a0001c0004t0001g0042others(3): Show | 6 | 266 | 0.0226 | -517 | c.298 others(17): Show |
B3GNTL1 | ENSG00000175711.9 | transcript | ENST00000320865.4 | protein_coding | 4/12 | chr17 | TogoVar | ||||||
BRSK2_chr11_1384934_1467689 | 1431346 | GTCTGGTC others(510): Show |
G | intron_variant | MODIFIER | NA19007.hp2 | a0002 | a0002c0002 | a0002c0002t0053 | a0002c0002t0053g0139 | 1 | 360 | 0.0028 | -517 | c.92- others(15): Show |
BRSK2 | ENSG00000174672.16 | transcript | ENST00000528841.6 | protein_coding | 1/19 | chr11 | TogoVar | ||||||
CCDC77_chr12_396644_447642 | 419407 | ACATGTTC others(510): Show |
A | intron_variant | MODIFIER | HG01884.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0401 | 1 | 432 | 0.0023 | -517 | c.413 others(16): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
CCDC77_chr12_396644_447642 | 419682 | AATACACA others(510): Show |
A | intron_variant | MODIFIER | HG02970.hp1 | a0005 | a0005c0005 | a0005c0005t0005 | a0005c0005t0005g0418 | 1 | 432 | 0.0023 | -517 | c.413 others(17): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ENPP2_chr8_119552086_119643839 | 119633438 | TGTGGTTA others(510): Show |
T | intron_variant | MODIFIER | HG02109.hp1 HG02559.hp2 HG02572.hp2 |
a0001 | a0001c0004 | a0001c0004t0002a0001c0004t0003 | a0001c0004t0002g0035a0001c0004t0003g0034a0001c0004t0003g0036 | 3 | 340 | 0.0088 | -517 | c.136 others(17): Show |
ENPP2 | ENSG00000136960.13 | transcript | ENST00000075322.11 | protein_coding | 2/24 | chr8 | TogoVar | ||||||
ERC1_chr12_986223_1500931 | 1085964 | GTTGTTGT others(510): Show |
G | intron_variant | MODIFIER | HG01993.hp1 | a0001 | a0001c0001 | a0001c0001t0083 | a0001c0001t0083g0130 | 1 | 162 | 0.0062 | -517 | c.108 others(19): Show |
ERC1 | ENSG00000082805.21 | transcript | ENST00000360905.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ERC1_chr12_986223_1500931 | 1087920 | GTTGTTGT others(510): Show |
G | intron_variant | MODIFIER | HG01496.hp1 HG02258.hp2 HG02895.hp1 others(3): Show |
a0001a0002a0008 | a0001c0001a0002c0002a0008c0011 | a0001c0001t0071a0002c0002t0042a0002c0002t0066others(3): Show | a0001c0001t0071g0074a0002c0002t0042g0079a0002c0002t0066g0139others(3): Show | 6 | 162 | 0.0370 | -517 | c.108 others(19): Show |
ERC1 | ENSG00000082805.21 | transcript | ENST00000360905.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ERC1_chr12_986223_1500931 | 1089678 | GTTGTTGT others(510): Show |
G | intron_variant | MODIFIER | HG03516.hp2 | a0002 | a0002c0007 | a0002c0007t0059 | a0002c0007t0059g0071 | 1 | 162 | 0.0062 | -517 | c.108 others(19): Show |
ERC1 | ENSG00000082805.21 | transcript | ENST00000360905.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ERC1_chr12_986223_1500931 | 1089808 | GTTGTTGT others(510): Show |
G | intron_variant | MODIFIER | HG01261.hp2 | a0001 | a0001c0001 | a0001c0001t0069 | a0001c0001t0069g0092 | 1 | 162 | 0.0062 | -517 | c.108 others(19): Show |
ERC1 | ENSG00000082805.21 | transcript | ENST00000360905.9 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
ERICH1_chr8_659200_736224 | 675616 | GGCCCCTC others(510): Show |
G | intron_variant | MODIFIER | HG01261.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0014 | 1 | 378 | 0.0027 | -517 | c.305 others(17): Show |
ERICH1 | ENSG00000104714.14 | transcript | ENST00000262109.8 | protein_coding | 3/5 | chr8 | TogoVar | ||||||
GAL3ST2_chr2_241771822_241809287 | 241805712 | TCCCCCCT others(510): Show |
T | downstream_gene_variant | MODIFIER | NA18983.hp2 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0236 | 1 | 314 | 0.0032 | -517 | c.*15 others(11): Show |
GAL3ST2 | ENSG00000154252.12 | transcript | ENST00000192314.7 | protein_coding | 1426 | chr2 | TogoVar | ||||||
HPD_chr12_121834527_121863859 | 121844957 | ACCTGTAA others(510): Show |
A | intron_variant | MODIFIER | HG01884.hp1 HG01891.hp2 HG02109.hp1 others(19): Show |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0001a0003c0003t0001 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(14): Show | 22 | 406 | 0.0542 | -517 | c.831 others(17): Show |
HPD | ENSG00000158104.11 | transcript | ENST00000289004.8 | protein_coding | 11/13 | chr12 | TogoVar | ||||||
LMBR1_chr7_156672791_156898183 | 156841920 | GAGAAAAA others(510): Show |
G | intron_variant | MODIFIER | HG00423.hp2 HG01081.hp1 HG01106.hp2 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0013a0001c0001t0033others(4): Show | a0001c0001t0008g0010a0001c0001t0008g0016a0001c0001t0013g0015others(10): Show | 13 | 314 | 0.0414 | -517 | c.67- others(15): Show |
LMBR1 | ENSG00000105983.23 | transcript | ENST00000353442.10 | protein_coding | 1/16 | chr7 | TogoVar | ||||||
NEU4_chr2_241804193_241822413 | 241805712 | TCCCCCCT others(510): Show |
T | upstream_gene_variant | MODIFIER | NA18983.hp2 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0024 | 1 | 319 | 0.0031 | -517 | c.-35 others(11): Show |
NEU4 | ENSG00000204099.12 | transcript | ENST00000407683.6 | protein_coding | 3480 | chr2 | TogoVar | ||||||
NFATC1_chr18_79390930_79534323 | 79417171 | GGGAGATG others(510): Show |
G | intron_variant | MODIFIER | HG02572.hp2 | a0001 | a0001c0006 | a0001c0006t0048 | a0001c0006t0048g0049 | 1 | 322 | 0.0031 | -517 | c.122 others(19): Show |
NFATC1 | ENSG00000131196.18 | transcript | ENST00000427363.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
OTUD7A_chr15_31470398_31875673 | 31511020 | TGTATATC others(510): Show |
T | intron_variant | MODIFIER | NA18522.hp1 | a0001 | a0001c0002 | a0001c0002t0020 | a0001c0002t0020g0168 | 1 | 244 | 0.0041 | -517 | c.894 others(17): Show |
OTUD7A | ENSG00000169918.10 | transcript | ENST00000307050.6 | protein_coding | 8/12 | chr15 | TogoVar | ||||||
RCOR1_chr14_102587649_102735561 | 102676518 | CCTCCCTC others(510): Show |
C | intron_variant | MODIFIER | HG03139.hp2 NA19043.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0012a0001c0004t0012 | a0001c0001t0012g0154a0001c0004t0012g0151 | 2 | 292 | 0.0069 | -517 | c.362 others(17): Show |
RCOR1 | ENSG00000089902.10 | transcript | ENST00000262241.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
TEKT5_chr16_10622501_10699930 | 10677215 | ATGAAAGA others(510): Show |
A | intron_variant | MODIFIER | HG00408.hp1 HG00544.hp2 HG00558.hp1 others(86): Show |
a0001a0003a0012 | a0001c0001a0001c0003a0001c0005others(3): Show | a0001c0001t0001a0001c0003t0001a0001c0005t0001others(3): Show | a0001c0001t0001g0096a0001c0003t0001g0003a0001c0003t0001g0147others(85): Show | 89 | 388 | 0.2294 | -517 | c.864 others(17): Show |
TEKT5 | ENSG00000153060.8 | transcript | ENST00000283025.7 | protein_coding | 4/6 | chr16 | TogoVar | ||||||
USH2A_chr1_215617891_216428448 | 216058135 | GTCCATAA others(510): Show |
G | intron_variant | MODIFIER | HG01109.hp1 HG02257.hp1 HG02257.hp2 others(9): Show |
a0015a0016a0018others(9): Show | a0015c0060a0016c0059a0018c0058others(9): Show | a0015c0060t0001a0016c0059t0001a0018c0058t0001others(9): Show | a0015c0060t0001g0067a0016c0059t0001g0069a0018c0058t0001g0068others(9): Show | 12 | 74 | 0.1622 | -517 | c.605 others(20): Show |
USH2A | ENSG00000042781.14 | transcript | ENST00000307340.8 | protein_coding | 30/71 | chr1 | TogoVar | ||||||
AP3D1_chr19_2095988_2156566 | 2128514 | AGCTCCGA others(509): Show |
A | intron_variant | MODIFIER | HG02258.hp1 NA18980.hp1 NA18989.hp1 others(1): Show |
a0001a0002 | a0001c0003a0002c0009 | a0001c0003t0002a0002c0009t0002 | a0001c0003t0002g0041a0001c0003t0002g0042a0001c0003t0002g0043others(1): Show | 4 | 406 | 0.0099 | -516 | c.806 others(14): Show |
AP3D1 | ENSG00000065000.20 | transcript | ENST00000643116.3 | protein_coding | 8/31 | chr19 | TogoVar | ||||||
C7orf50_chr7_992006_1143247 | 1128629 | GGCTCATC others(509): Show |
G | intron_variant | MODIFIER | NA18971.hp1 NA18986.hp1 NA19007.hp2 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0027 | a0001c0001t0004g0184a0001c0001t0004g0185a0001c0001t0027g0193 | 3 | 326 | 0.0092 | -516 | c.-1- others(15): Show |
C7orf50 | ENSG00000146540.15 | transcript | ENST00000397098.8 | protein_coding | 1/4 | chr7 | TogoVar | ||||||
C7orf50_chr7_992006_1143247 | 1128729 | CCACCCTG others(509): Show |
C | intron_variant | MODIFIER | NA19043.hp2 | a0006 | a0006c0006 | a0006c0006t0005 | a0006c0006t0005g0296 | 1 | 326 | 0.0031 | -516 | c.-1- others(15): Show |
C7orf50 | ENSG00000146540.15 | transcript | ENST00000397098.8 | protein_coding | 1/4 | chr7 | TogoVar | ||||||
CACNG7_chr19_53904278_53948950 | 53922141 | GAGTTGTC others(509): Show |
G | intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062 | 1 | 364 | 0.0028 | -516 | c.424 others(17): Show |
CACNG7 | ENSG00000105605.8 | transcript | ENST00000391767.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
FOXN3_chr14_89151177_89422233 | 89360856 | CCACCACC others(509): Show |
C | intron_variant | MODIFIER | NA18964.hp1 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0033 | 1 | 230 | 0.0044 | -516 | c.544 others(19): Show |
FOXN3 | ENSG00000053254.16 | transcript | ENST00000557258.6 | protein_coding | 2/5 | chr14 | TogoVar | ||||||
FOXN3_chr14_89151177_89422233 | 89361852 | ACTACCTC others(509): Show |
A | intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0001 | a0001c0001t0057 | a0001c0001t0057g0018 | 1 | 230 | 0.0044 | -516 | c.544 others(19): Show |
FOXN3 | ENSG00000053254.16 | transcript | ENST00000557258.6 | protein_coding | 2/5 | chr14 | TogoVar | ||||||
GAL3ST2_chr2_241771822_241809287 | 241805486 | TCCCCCCT others(509): Show |
T | downstream_gene_variant | MODIFIER | HG01069.hp2 HG02155.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006a0001c0001t0001g0193 | 2 | 314 | 0.0064 | -516 | c.*13 others(11): Show |
GAL3ST2 | ENSG00000154252.12 | transcript | ENST00000192314.7 | protein_coding | 1200 | chr2 | TogoVar | ||||||
GAL3ST2_chr2_241771822_241809287 | 241805524 | CTCCCCCC others(509): Show |
C | downstream_gene_variant | MODIFIER | HG04115.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005 | 1 | 314 | 0.0032 | -516 | c.*13 others(11): Show |
GAL3ST2 | ENSG00000154252.12 | transcript | ENST00000192314.7 | protein_coding | 1238 | chr2 | TogoVar | ||||||
HSD17B14_chr19_48808018_48841491 | 48834421 | TTGGACTC others(509): Show |
T | intron_variant | MODIFIER | NA19240.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0227 | 1 | 394 | 0.0025 | -516 | c.128 others(14): Show |
HSD17B14 | ENSG00000087076.9 | transcript | ENST00000263278.9 | protein_coding | 2/8 | chr19 | TogoVar | ||||||
HSD17B14_chr19_48808018_48841491 | 48834558 | GGCTGGGA others(509): Show |
G | intron_variant | MODIFIER | HG03041.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0247 | 1 | 394 | 0.0025 | -516 | c.128 others(15): Show |
HSD17B14 | ENSG00000087076.9 | transcript | ENST00000263278.9 | protein_coding | 2/8 | chr19 | TogoVar | ||||||
LMLN_chr3_197955217_198048720 | 198004457 | CCATCTAT others(509): Show |
C | intron_variant | MODIFIER | NA18951.hp1 NA19090.hp2 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0241a0001c0001t0004g0245 | 2 | 258 | 0.0078 | -516 | c.131 others(19): Show |
LMLN | ENSG00000185621.11 | transcript | ENST00000420910.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
MAPK8IP3_chr16_1701195_1775351 | 1737938 | CCGTGTGA others(509): Show |
C | intron_variant | MODIFIER | HG00423.hp2 | a0001 | a0001c0003 | a0001c0003t0009 | a0001c0003t0009g0290 | 1 | 330 | 0.0030 | -516 | c.603 others(17): Show |
MAPK8IP3 | ENSG00000138834.15 | transcript | ENST00000610761.2 | protein_coding | 4/31 | chr16 | TogoVar | ||||||
MS4A6E_chr11_60322255_60346341 | 60329929 | GATTCTCC others(509): Show |
G | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(25): Show |
a0001 | a0001c0003 | a0001c0003t0002a0001c0003t0006a0001c0003t0011 | a0001c0003t0002g0028a0001c0003t0002g0055a0001c0003t0002g0056others(16): Show | 28 | 450 | 0.0622 | -516 | c.-15 others(17): Show |
MS4A6E | ENSG00000166926.9 | transcript | ENST00000684409.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
NEU4_chr2_241804193_241822413 | 241805524 | CTCCCCCC others(509): Show |
C | upstream_gene_variant | MODIFIER | HG04115.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0008 | 1 | 319 | 0.0031 | -516 | c.-37 others(11): Show |
NEU4 | ENSG00000204099.12 | transcript | ENST00000407683.6 | protein_coding | 3668 | chr2 | TogoVar | ||||||
OTUD7A_chr15_31470398_31875673 | 31511168 | CATATGTA others(509): Show |
C | intron_variant | MODIFIER | HG01123.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0114 | 1 | 244 | 0.0041 | -516 | c.894 others(17): Show |
OTUD7A | ENSG00000169918.10 | transcript | ENST00000307050.6 | protein_coding | 8/12 | chr15 | TogoVar |