| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| ADAMTS3_chr4_72275969_72574221 | 72550030 | AGAAGAAG others(44): Show |
A | intron_variant | MODIFIER | HG02976.hp2 HG03453.hp1 NA18992.hp1 |
a0001a0005a0009 | a0001c0001a0005c0018a0009c0014 | a0001c0001t0001a0005c0018t0018a0009c0014t0031 | a0001c0001t0001g0113a0005c0018t0018g0031a0009c0014t0031g0074 | 3 | 182 | 0.0165 | -51 | c.98- others(66): Show |
ADAMTS3 | ENSG00000156140.11 | transcript | ENST00000286657.10 | protein_coding | 2/21 | chr4 | TogoVar | ||||||
| ADAMTS3_chr4_72275969_72574221 | 72550045 | GGAAGAGG others(44): Show |
G | intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0082 | 1 | 182 | 0.0055 | -51 | c.98- others(66): Show |
ADAMTS3 | ENSG00000156140.11 | transcript | ENST00000286657.10 | protein_coding | 2/21 | chr4 | TogoVar | ||||||
| ADAMTSL3_chr15_83649123_84044842 | 83823893 | CTCTTCTT others(44): Show |
C | intron_variant | MODIFIER | HG02486.hp1 NA19030.hp1 NA20300.hp2 |
a0002a0019 | a0002c0008a0019c0022 | a0002c0008t0001a0019c0022t0001a0019c0022t0012 | a0002c0008t0001g0115a0019c0022t0001g0242a0019c0022t0012g0235 | 3 | 274 | 0.0110 | -51 | c.600 others(68): Show |
ADAMTSL3 | ENSG00000156218.13 | transcript | ENST00000286744.10 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
| ADCY9_chr16_3957653_4121442 | 3987966 | CTGGGACT others(44): Show |
C | intron_variant | MODIFIER | HG02109.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0022others(1): Show | a0001c0001t0019a0001c0002t0002a0001c0022t0100others(1): Show | a0001c0001t0019g0018a0001c0002t0002g0281a0001c0022t0100g0249others(1): Show | 4 | 320 | 0.0125 | -51 | c.231 others(69): Show |
ADCY9 | ENSG00000162104.10 | transcript | ENST00000294016.8 | protein_coding | 6/10 | chr16 | TogoVar | ||||||
| ADGB_chr6_146593972_146820462 | 146691441 | TAAAAATA others(44): Show |
T | intron_variant | MODIFIER | HG02647.hp1 | a0025 | a0025c0054 | a0025c0054t0002 | a0025c0054t0002g0021 | 1 | 276 | 0.0036 | -51 | c.148 others(68): Show |
ADGB | ENSG00000118492.19 | transcript | ENST00000397944.8 | protein_coding | 11/35 | chr6 | TogoVar | ||||||
| ADGB_chr6_146593972_146820462 | 146787618 | CTCTTATT others(44): Show |
C | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(217): Show |
a0001a0002a0003others(26): Show | a0001c0001a0001c0002a0001c0004others(67): Show | a0001c0001t0002a0001c0002t0002a0001c0004t0002others(75): Show | a0001c0001t0002g0135a0001c0001t0002g0139a0001c0001t0002g0140others(216): Show | 220 | 276 | 0.7971 | -51 | c.431 others(68): Show |
ADGB | ENSG00000118492.19 | transcript | ENST00000397944.8 | protein_coding | 32/35 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
| ADGRA1_chr10_133082924_133136675 | 133108808 | ATCCTCCA others(44): Show |
A | intron_variant | MODIFIER | HG01074.hp2 HG01081.hp1 HG01099.hp2 others(30): Show |
a0001a0008 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0002a0001c0001t0011a0001c0001t0076others(12): Show | a0001c0001t0002g0113a0001c0001t0002g0214a0001c0001t0002g0217others(29): Show | 33 | 368 | 0.0897 | -51 | c.401 others(68): Show |
ADGRA1 | ENSG00000197177.16 | transcript | ENST00000392607.8 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
| ADGRD1_chr12_130948907_131146469 | 131095994 | CGCCTCCC others(44): Show |
C | intron_variant | MODIFIER | HG03831.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0195 | 1 | 242 | 0.0041 | -51 | c.167 others(70): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
| ADGRD1_chr12_130948907_131146469 | 131096002 | AGCCCTGC others(44): Show |
A | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(93): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | a0001c0001t0001g0113a0001c0001t0001g0208a0001c0001t0002g0005others(93): Show | 96 | 242 | 0.3967 | -51 | c.167 others(70): Show |
ADGRD1 | ENSG00000111452.13 | transcript | ENST00000261654.10 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
| AGRN_chr1_1015120_1061116 | 1053192 | GGTGTCTG others(44): Show |
G | intron_variant | MODIFIER | HG01074.hp1 HG01123.hp1 HG01884.hp2 others(15): Show |
a0002a0006a0008others(5): Show | a0002c0005a0002c0062a0006c0010others(6): Show | a0002c0005t0004a0002c0062t0011a0006c0010t0007others(6): Show | a0002c0005t0004g0176a0002c0005t0004g0185a0002c0005t0004g0186others(15): Show | 18 | 210 | 0.0857 | -51 | c.565 others(68): Show |
AGRN | ENSG00000188157.15 | transcript | ENST00000379370.7 | protein_coding | 33/35 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
| AK5_chr1_77277019_77564966 | 77444303 | ATATATAC others(44): Show |
A | intron_variant | MODIFIER | HG02818.hp2 HG03540.hp1 HG06807.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002 | a0001c0001t0001g0001a0001c0001t0001g0224a0002c0002t0002g0225 | 3 | 284 | 0.0106 | -51 | c.105 others(72): Show |
AK5 | ENSG00000154027.19 | transcript | ENST00000354567.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
| ALOXE3_chr17_8090900_8123514 | 8107914 | AAAGAAAG others(44): Show |
A | intron_variant | MODIFIER | HG02129.hp2 NA19088.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0142a0001c0001t0002g0214 | 2 | 422 | 0.0047 | -51 | c.168 others(68): Show |
ALOXE3 | ENSG00000179148.10 | transcript | ENST00000448843.7 | protein_coding | 13/15 | chr17 | TogoVar | ||||||
| ALPP_chr2_232373751_232387889 | 232385470 | GTTTCGCT others(44): Show |
G | downstream_gene_variant | MODIFIER | HG02015.hp2 | a0003 | a0003c0003 | a0003c0003t0002 | a0003c0003t0002g0006 | 1 | 410 | 0.0024 | -51 | c.*36 others(62): Show |
ALPP | ENSG00000163283.7 | transcript | ENST00000392027.3 | protein_coding | 2582 | chr2 | TogoVar | ||||||
| AMPH_chr7_38378704_38636373 | 38541287 | AGTGCAGG others(44): Show |
A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0040others(106): Show | 109 | 288 | 0.3785 | -51 | c.70- others(66): Show |
AMPH | ENSG00000078053.17 | transcript | ENST00000356264.7 | protein_coding | 1/20 | chr7 | TogoVar | ||||||
| ANKFN1_chr17_56148475_56522016 | 56467743 | CAAAGAAA others(44): Show |
C | intron_variant | MODIFIER | HG03139.hp2 | a0003 | a0003c0003 | a0003c0003t0003 | a0003c0003t0003g0112 | 1 | 112 | 0.0089 | -51 | c.177 others(70): Show |
ANKFN1 | ENSG00000153930.13 | transcript | ENST00000682825.1 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
| ANKRD11_chr16_89262630_89495561 | 89328539 | TGGGTGAA others(44): Show |
T | intron_variant | MODIFIER | HG03041.hp1 HG03453.hp2 NA20129.hp2 |
a0001a0002 | a0001c0007a0002c0002 | a0001c0007t0001a0002c0002t0001 | a0001c0007t0001g0092a0002c0002t0001g0064a0002c0002t0001g0065 | 3 | 310 | 0.0097 | -51 | c.-59 others(70): Show |
ANKRD11 | ENSG00000167522.17 | transcript | ENST00000301030.10 | protein_coding | 2/12 | chr16 | TogoVar | ||||||
| ANKRD31_chr5_75063297_75241878 | 75206227 | AAAAAAAA others(44): Show |
A | intron_variant | MODIFIER | HG02523.hp2 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0169 | 1 | 334 | 0.0030 | -51 | c.403 others(66): Show |
ANKRD31 | ENSG00000145700.10 | transcript | ENST00000506364.6 | protein_coding | 5/25 | chr5 | TogoVar | ||||||
| ANKRD31_chr5_75063297_75241878 | 75206229 | AAAAAAAA others(44): Show |
A | intron_variant | MODIFIER | HG01943.hp1 HG02148.hp2 HG02809.hp2 others(3): Show |
a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0099a0003c0003t0001g0127a0003c0003t0001g0133others(3): Show | 6 | 334 | 0.0180 | -51 | c.403 others(66): Show |
ANKRD31 | ENSG00000145700.10 | transcript | ENST00000506364.6 | protein_coding | 5/25 | chr5 | TogoVar | ||||||
| ANKRD31_chr5_75063297_75241878 | 75206231 | AAAAAAAA others(44): Show |
A | intron_variant | MODIFIER | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(32): Show |
a0003a0014a0025 | a0003c0003a0014c0017a0025c0025 | a0003c0003t0001a0014c0017t0001a0025c0025t0001 | a0003c0003t0001g0002a0003c0003t0001g0057a0003c0003t0001g0095others(31): Show | 35 | 334 | 0.1048 | -51 | c.403 others(66): Show |
ANKRD31 | ENSG00000145700.10 | transcript | ENST00000506364.6 | protein_coding | 5/25 | chr5 | TogoVar | ||||||
| ANKRD31_chr5_75063297_75241878 | 75206233 | AAAAAAAA others(44): Show |
A | intron_variant | MODIFIER | NA18999.hp2 NA19009.hp2 |
a0003a0029 | a0003c0003a0029c0029 | a0003c0003t0001a0029c0029t0001 | a0003c0003t0001g0136a0029c0029t0001g0125 | 2 | 334 | 0.0060 | -51 | c.403 others(66): Show |
ANKRD31 | ENSG00000145700.10 | transcript | ENST00000506364.6 | protein_coding | 5/25 | chr5 | TogoVar | ||||||
| ANKRD31_chr5_75063297_75241878 | 75206235 | AAAAAAAA others(44): Show |
A | intron_variant | MODIFIER | HG03209.hp2 | a0004 | a0004c0005 | a0004c0005t0001 | a0004c0005t0001g0305 | 1 | 334 | 0.0030 | -51 | c.403 others(66): Show |
ANKRD31 | ENSG00000145700.10 | transcript | ENST00000506364.6 | protein_coding | 5/25 | chr5 | TogoVar | ||||||
| ANKRD31_chr5_75063297_75241878 | 75206237 | AAAAAAAA others(44): Show |
A | intron_variant | MODIFIER | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(3): Show |
a0004a0006 | a0004c0005a0006c0006 | a0004c0005t0001a0006c0006t0001 | a0004c0005t0001g0005a0004c0005t0001g0304a0004c0005t0001g0308others(2): Show | 6 | 334 | 0.0180 | -51 | c.403 others(66): Show |
ANKRD31 | ENSG00000145700.10 | transcript | ENST00000506364.6 | protein_coding | 5/25 | chr5 | TogoVar | ||||||
| ANXA10_chr4_168087537_168192736 | 168155444 | TGAATTAT others(44): Show |
T | intron_variant | MODIFIER | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0117others(15): Show | 18 | 284 | 0.0634 | -51 | c.196 others(68): Show |
ANXA10 | ENSG00000109511.12 | transcript | ENST00000359299.8 | protein_coding | 3/11 | chr4 | TogoVar | ||||||
| APBB2_chr4_40805027_41219542 | 40982194 | GGAAAGAA others(44): Show |
G | intron_variant | MODIFIER | HG00280.hp2 HG00544.hp1 HG00597.hp2 others(6): Show |
a0001a0002 | a0001c0002a0001c0003a0002c0001others(1): Show | a0001c0002t0001a0001c0002t0010a0001c0003t0001others(3): Show | a0001c0002t0001g0039a0001c0002t0001g0070a0001c0002t0010g0006others(6): Show | 9 | 192 | 0.0469 | -51 | c.835 others(70): Show |
APBB2 | ENSG00000163697.18 | transcript | ENST00000508593.6 | protein_coding | 6/17 | chr4 | TogoVar | ||||||
| APLP2_chr11_130064894_130149805 | 130091192 | GACGGGGC others(44): Show |
G | intron_variant | MODIFIER | NA19010.hp2 | a0004 | a0004c0004 | a0004c0004t0003 | a0004c0004t0003g0166 | 1 | 274 | 0.0037 | -51 | c.106 others(70): Show |
APLP2 | ENSG00000084234.18 | transcript | ENST00000338167.10 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
| APOL5_chr22_35712872_35734483 | 35726258 | TCAACTGT others(44): Show |
T | stop_gained others(1): Show |
HIGH | HG01261.hp2 | a0008 | a0008c0010 | a0008c0010t0001 | a0008c0010t0001g0003 | 1 | 401 | 0.0025 | -51 | c.191 others(58): Show |
p.Ser others(17): Show |
APOL5 | ENSG00000128313.2 | transcript | ENST00000249044.2 | protein_coding | 3/5 | 191/1438 | 191/1302 | 64/433 | chr22 | TogoVar | ||
| ARC_chr8_142606049_142619479 | 142609957 | AAAGTCAG others(44): Show |
A | downstream_gene_variant | MODIFIER | NA18993.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0002 | 1 | 420 | 0.0024 | -51 | c.*25 others(62): Show |
ARC | ENSG00000198576.4 | transcript | ENST00000356613.4 | protein_coding | 1091 | chr8 | TogoVar | ||||||
| ARHGAP39_chr8_144524179_144690846 | 144625076 | GGTTCACG others(44): Show |
G | intron_variant | MODIFIER | HG01168.hp2 HG02145.hp2 HG02486.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0010 | a0001c0001t0001a0001c0001t0016a0001c0002t0001others(1): Show | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0016g0105others(4): Show | 7 | 246 | 0.0285 | -51 | c.-81 others(70): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
| ARHGAP39_chr8_144524179_144690846 | 144625425 | GGCGGCCC others(44): Show |
G | intron_variant | MODIFIER | HG03041.hp1 NA19043.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0024a0001c0002t0001g0025 | 2 | 246 | 0.0081 | -51 | c.-81 others(70): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
| ARHGAP39_chr8_144524179_144690846 | 144625586 | GGTTCACG others(44): Show |
G | intron_variant | MODIFIER | HG02257.hp1 | a0001 | a0001c0007 | a0001c0007t0003 | a0001c0007t0003g0078 | 1 | 246 | 0.0041 | -51 | c.-81 others(70): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
| ARHGAP39_chr8_144524179_144690846 | 144625651 | TCACTGCA others(44): Show |
T | intron_variant | MODIFIER | HG00558.hp2 HG01168.hp2 HG01346.hp2 others(1): Show |
a0001a0002 | a0001c0002a0001c0010a0002c0008 | a0001c0002t0001a0001c0010t0001a0002c0008t0001 | a0001c0002t0001g0003a0001c0002t0001g0124a0001c0010t0001g0009others(1): Show | 4 | 246 | 0.0163 | -51 | c.-81 others(70): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
| ARHGAP39_chr8_144524179_144690846 | 144625680 | GGCGGCCC others(44): Show |
G | intron_variant | MODIFIER | HG02155.hp1 | a0002 | a0002c0008 | a0002c0008t0001 | a0002c0008t0001g0067 | 1 | 246 | 0.0041 | -51 | c.-81 others(70): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
| ARHGAP39_chr8_144524179_144690846 | 144625790 | CGTTCACG others(44): Show |
C | intron_variant | MODIFIER | HG02155.hp1 | a0002 | a0002c0008 | a0002c0008t0001 | a0002c0008t0001g0067 | 1 | 246 | 0.0041 | -51 | c.-81 others(70): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
| ARHGAP39_chr8_144524179_144690846 | 144625935 | CGCGGCCC others(44): Show |
C | intron_variant | MODIFIER | HG02572.hp1 HG02976.hp2 HG03195.hp1 others(2): Show |
a0001 | a0001c0001a0001c0014 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(2): Show | a0001c0001t0001g0238a0001c0001t0002g0241a0001c0001t0004g0237others(2): Show | 5 | 246 | 0.0203 | -51 | c.-81 others(70): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
| ARHGAP39_chr8_144524179_144690846 | 144625957 | TCACTGCA others(44): Show |
T | intron_variant | MODIFIER | HG02109.hp1 HG02615.hp2 HG02622.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0018 | a0001c0001t0001a0001c0002t0001a0001c0018t0001 | a0001c0001t0001g0024a0001c0001t0001g0228a0001c0001t0001g0229others(6): Show | 9 | 246 | 0.0366 | -51 | c.-81 others(70): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
| ARHGAP39_chr8_144524179_144690846 | 144626128 | GCCCCTGT others(44): Show |
G | intron_variant | MODIFIER | HG02258.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0002t0001 | a0001c0001t0003g0084a0001c0002t0001g0082a0001c0002t0001g0083others(1): Show | 4 | 246 | 0.0163 | -51 | c.-81 others(70): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
| ARHGAP39_chr8_144524179_144690846 | 144626314 | TCACTGCA others(44): Show |
T | intron_variant | MODIFIER | HG02258.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0122a0001c0001t0002g0123a0001c0001t0003g0084others(4): Show | 7 | 246 | 0.0285 | -51 | c.-81 others(70): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
| ARHGAP39_chr8_144524179_144690846 | 144626467 | CCACTGCA others(44): Show |
C | intron_variant | MODIFIER | NA18522.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0021 | 1 | 246 | 0.0041 | -51 | c.-81 others(70): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
| ARHGEF10_chr8_1818926_1963641 | 1889152 | GAGGAGAC others(44): Show |
G | intron_variant | MODIFIER | HG02647.hp2 | a0010 | a0010c0097 | a0010c0097t0014 | a0010c0097t0014g0205 | 1 | 363 | 0.0028 | -51 | c.118 others(70): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
| ARHGEF10_chr8_1818926_1963641 | 1955050 | GTAGCTAG others(44): Show |
G | intron_variant | MODIFIER | HG01255.hp1 HG01346.hp2 HG01993.hp1 others(8): Show |
a0001a0015a0021 | a0001c0003a0001c0007a0001c0013others(3): Show | a0001c0003t0001a0001c0003t0026a0001c0007t0003others(4): Show | a0001c0003t0001g0059a0001c0003t0026g0190a0001c0007t0003g0143others(8): Show | 11 | 363 | 0.0303 | -51 | c.352 others(70): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
| ARHGEF10_chr8_1818926_1963641 | 1955055 | TAGGTGCT others(44): Show |
T | intron_variant | MODIFIER | HG00741.hp2 HG01496.hp2 HG02257.hp1 others(8): Show |
a0001a0005a0009others(1): Show | a0001c0002a0001c0003a0001c0005others(5): Show | a0001c0002t0020a0001c0003t0035a0001c0003t0068others(8): Show | a0001c0002t0020g0206a0001c0003t0035g0180a0001c0003t0068g0338others(8): Show | 11 | 363 | 0.0303 | -51 | c.352 others(70): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
| ARHGEF10_chr8_1818926_1963641 | 1955241 | TGTTCCTC others(44): Show |
T | intron_variant | MODIFIER | NA19074.hp1 | a0001 | a0001c0015 | a0001c0015t0001 | a0001c0015t0001g0281 | 1 | 363 | 0.0028 | -51 | c.352 others(70): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
| ARHGEF18_chr19_7343937_7477478 | 7359451 | GCCAGATC others(44): Show |
G | intron_variant | MODIFIER | HG01891.hp1 HG02280.hp1 HG02451.hp2 others(5): Show |
a0002a0026 | a0002c0004a0002c0006a0026c0029 | a0002c0004t0021a0002c0006t0007a0026c0029t0020 | a0002c0004t0021g0277a0002c0006t0007g0270a0002c0006t0007g0271others(5): Show | 8 | 298 | 0.0269 | -51 | c.-11 others(70): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
| ARHGEF7_chr13_111110310_111310732 | 111254361 | CCACTAAC others(44): Show |
C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0004others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(199): Show | 202 | 274 | 0.7372 | -51 | c.950 others(70): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
| ARHGEF7_chr13_111110310_111310732 | 111254586 | TCAGAAGA others(44): Show |
T | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG01109.hp1 others(18): Show |
a0001 | a0001c0001a0001c0002a0001c0014 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0084a0001c0001t0001g0144a0001c0001t0002g0011others(18): Show | 21 | 274 | 0.0766 | -51 | c.950 others(70): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
| ARL6_chr3_97759758_97806229 | 97781300 | GTCAAGTG others(44): Show |
G | intron_variant | MODIFIER | HG00423.hp2 HG00733.hp2 HG02165.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0007a0001c0001t0012others(1): Show | a0001c0001t0006g0061a0001c0001t0006g0062a0001c0001t0006g0063others(7): Show | 11 | 364 | 0.0302 | -51 | c.254 others(66): Show |
ARL6 | ENSG00000113966.11 | transcript | ENST00000463745.6 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
| ARL9_chr4_56500791_56529453 | 56526402 | TAACGATG others(44): Show |
T | downstream_gene_variant | MODIFIER | NA20752.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041 | 1 | 416 | 0.0024 | -51 | c.*25 others(62): Show |
ARL9 | ENSG00000196503.5 | transcript | ENST00000640821.3 | protein_coding | 1950 | chr4 | TogoVar | ||||||
| ART1_chr11_3640128_3669416 | 3653290 | GATGGCCG others(44): Show |
G | intron_variant | MODIFIER | NA18949.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0158 | 1 | 394 | 0.0025 | -51 | c.-52 others(68): Show |
ART1 | ENSG00000129744.3 | transcript | ENST00000250693.2 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
| AS3MT_chr10_102864470_102906899 | 102877751 | TTTTTTTT others(44): Show |
T | intron_variant | MODIFIER | NA18965.hp1 | a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0079 | 1 | 362 | 0.0028 | -51 | c.611 others(66): Show |
AS3MT | ENSG00000214435.9 | transcript | ENST00000369880.8 | protein_coding | 7/10 | chr10 | TogoVar | ||||||
| ASAP2_chr2_9201812_9410678 | 9249728 | AGGCATGC others(44): Show |
A | intron_variant | MODIFIER | HG01106.hp1 | a0002 | a0002c0005 | a0002c0005t0001 | a0002c0005t0001g0132 | 1 | 210 | 0.0048 | -51 | c.127 others(70): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |