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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SART1_chr11_65956734_65985137 | 65971177 | A | AAGCTGAG others(4080): Show |
intron_variant | MODIFIER | HG00558.hp1 | a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0247 | 1 | 105 | 0.0095 | 4087 | c.157 others(4106): Show |
SART1 | ENSG00000175467.15 | transcript | ENST00000312397.10 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
BAHCC1_chr17_81390457_81471331 | 81426076 | T | TGGTGATG others(4081): Show |
intron_variant | MODIFIER | NA18967.hp1 | a0002 | a0002c0026 | a0002c0026t0003 | a0002c0026t0003g0246 | 1 | 42 | 0.0238 | 4088 | c.179 others(4103): Show |
BAHCC1 | ENSG00000266074.11 | transcript | ENST00000675386.2 | protein_coding | 2/27 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4081): Show |
intron_variant | MODIFIER | HG00673.hp2 | a0001 | a0001c0002 | a0001c0002t0079 | a0001c0002t0079g0009 | 1 | 7 | 0.1429 | 4088 | c.-17 others(4107): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4081): Show |
intron_variant | MODIFIER | HG03225.hp1 | a0002 | a0002c0003 | a0002c0003t0007 | a0002c0003t0007g0103 | 1 | 7 | 0.1429 | 4088 | c.-17 others(4107): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4081): Show |
intron_variant | MODIFIER | NA18940.hp1 | a0001 | a0001c0002 | a0001c0002t0080 | a0001c0002t0080g0003 | 1 | 7 | 0.1429 | 4088 | c.-17 others(4107): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4081): Show |
intron_variant | MODIFIER | HG01169.hp2 | a0016 | a0016c0015 | a0016c0015t0083 | a0016c0015t0083g0007 | 1 | 7 | 0.1429 | 4088 | c.-17 others(4107): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CELSR1_chr22_46356174_46542620 | 46469974 | A | AGGGAGGA others(4082): Show |
intron_variant | MODIFIER | HG02976.hp1 | a0028 | a0028c0021 | a0028c0021t0001 | a0028c0021t0001g0061 | 1 | 13 | 0.0769 | 4089 | c.354 others(4108): Show |
CELSR1 | ENSG00000075275.18 | transcript | ENST00000674500.2 | protein_coding | 1/34 | chr22 | TogoVar | |||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4083): Show |
intron_variant | MODIFIER | HG02080.hp1 | a0018 | a0018c0028 | a0018c0028t0078 | a0018c0028t0078g0005 | 1 | 7 | 0.1429 | 4090 | c.-17 others(4109): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ABR_chr17_998519_1184981 | 1064992 | G | GCATGTTC others(4084): Show |
intron_variant | MODIFIER | HG03017.hp2 | a0001 | a0001c0001 | a0001c0001t0060 | a0001c0001t0060g0148 | 1 | 271 | 0.0037 | 4091 | c.118 others(4110): Show |
ABR | ENSG00000159842.16 | transcript | ENST00000302538.10 | protein_coding | 10/22 | chr17 | TogoVar | |||||||
C2orf80_chr2_208160347_208195030 | 208176945 | A | ATACATAT others(4084): Show |
intron_variant | MODIFIER | NA19010.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0169 | 1 | 329 | 0.0030 | 4091 | c.366 others(4108): Show |
C2orf80 | ENSG00000188674.11 | transcript | ENST00000341287.9 | protein_coding | 6/8 | chr2 | TogoVar | |||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4084): Show |
intron_variant | MODIFIER | NA18522.hp2 | a0004 | a0004c0012 | a0004c0012t0002 | a0004c0012t0002g0052 | 1 | 7 | 0.1429 | 4091 | c.-17 others(4110): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(4084): Show |
intron_variant | MODIFIER | HG02145.hp2 HG02922.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0065 a0001c0001t0001g0209 |
2 | 63 | 0.0317 | 4091 | c.286 others(4108): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(4084): Show |
intron_variant | MODIFIER | NA18942.hp1 NA20752.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0200 a0001c0001t0006g0271 |
2 | 63 | 0.0317 | 4091 | c.286 others(4108): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(4084): Show |
intron_variant | MODIFIER | HG01981.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0231 | 1 | 62 | 0.0161 | 4091 | c.286 others(4108): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ZFPM1_chr16_88448280_88542031 | 88501188 | C | CATCCCGC others(4084): Show |
intron_variant | MODIFIER | NA20129.hp2 | a0007 | a0007c0026 | a0007c0026t0007 | a0007c0026t0007g0126 | 1 | 296 | 0.0034 | 4091 | c.268 others(4110): Show |
ZFPM1 | ENSG00000179588.9 | transcript | ENST00000319555.8 | protein_coding | 3/9 | chr16 | TogoVar | |||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4085): Show |
intron_variant | MODIFIER | HG02723.hp1 | a0006 | a0006c0004 | a0006c0004t0006 | a0006c0004t0006g0087 | 1 | 7 | 0.1429 | 4092 | c.-17 others(4111): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4085): Show |
intron_variant | MODIFIER | HG02080.hp2 | a0004 | a0004c0012 | a0004c0012t0004 | a0004c0012t0004g0033 | 1 | 7 | 0.1429 | 4092 | c.-17 others(4111): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
JAG2_chr14_105135995_105173776 | 105162569 | G | GCACCCCA others(4085): Show |
intron_variant | MODIFIER | HG02976.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0233 | 1 | 362 | 0.0028 | 4092 | c.418 others(4109): Show |
JAG2 | ENSG00000184916.9 | transcript | ENST00000331782.8 | protein_coding | 2/25 | chr14 | TogoVar | |||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4086): Show |
intron_variant | MODIFIER | HG02055.hp2 | a0009 | a0009c0039 | a0009c0039t0029 | a0009c0039t0029g0106 | 1 | 7 | 0.1429 | 4093 | c.-17 others(4112): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
DISC1_chr1_231621790_232046272 | 231799889 | T | TTCCCTCC others(4087): Show |
intron_variant | MODIFIER | HG04204.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0038 | 1 | 3 | 0.3333 | 4094 | c.169 others(4111): Show |
DISC1 | ENSG00000162946.24 | transcript | ENST00000439617.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
FAT3_chr11_92219818_92901473 | 92329738 | G | GACTTTAG others(4087): Show |
intron_variant | MODIFIER | HG02809.hp1 | a0003 | a0003c0032 | a0003c0032t0012 | a0003c0032t0012g0109 | 1 | 7 | 0.1429 | 4094 | c.-17 others(4113): Show |
FAT3 | ENSG00000165323.16 | transcript | ENST00000525166.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
MICAL3_chr22_17782649_18029561 | 17876946 | T | TGGAGGTT others(4088): Show |
intron_variant | MODIFIER | NA18960.hp1 | a0003 | a0003c0047 | a0003c0047t0001 | a0003c0047t0001g0228 | 1 | 175 | 0.0057 | 4095 | c.224 others(4114): Show |
MICAL3 | ENSG00000243156.9 | transcript | ENST00000441493.7 | protein_coding | 16/31 | chr22 | TogoVar | |||||||
SERINC2_chr1_31408213_31439678 | 31432120 | T | TAGGGTGG others(4088): Show |
intron_variant | MODIFIER | NA18948.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0252 | 1 | 313 | 0.0032 | 4095 | c.101 others(4112): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
DISC1_chr1_231621790_232046272 | 231799889 | T | TTCCCTCC others(4089): Show |
intron_variant | MODIFIER | HG02559.hp2 | a0001 | a0001c0005 | a0001c0005t0006 | a0001c0005t0006g0033 | 1 | 3 | 0.3333 | 4096 | c.169 others(4113): Show |
DISC1 | ENSG00000162946.24 | transcript | ENST00000439617.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SLC6A3_chr5_1387794_1450440 | 1414399 | G | GGGGGGCC others(4089): Show |
intron_variant | MODIFIER | HG02027.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062 | 1 | 312 | 0.0032 | 4096 | c.115 others(4113): Show |
SLC6A3 | ENSG00000142319.18 | transcript | ENST00000270349.12 | protein_coding | 8/14 | chr5 | TogoVar | |||||||
PPFIA1_chr11_70265690_70389396 | 70371393 | T | TGGTGGCG others(4091): Show |
intron_variant | MODIFIER | HG01243.hp1 | a0001 | a0001c0003 | a0001c0003t0011 | a0001c0003t0011g0042 | 1 | 62 | 0.0161 | 4098 | c.286 others(4115): Show |
PPFIA1 | ENSG00000131626.19 | transcript | ENST00000253925.12 | protein_coding | 21/27 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
CRTC3_chr15_90524923_90650345 | 90647402 | C | CCCTCCTC others(4093): Show |
downstream_gene_variant | MODIFIER | HG02027.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0176 | 1 | 69 | 0.0145 | 4100 | c.*52 others(4111): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2058 | chr15 | TogoVar | |||||||
LRRC27_chr10_132327193_132386508 | 132364519 | G | GCACTTAC others(4093): Show |
intron_variant | MODIFIER | HG00423.hp2 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0231 | 1 | 207 | 0.0048 | 4100 | c.129 others(4117): Show |
LRRC27 | ENSG00000148814.18 | transcript | ENST00000368614.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
PIP5K1C_chr19_3625183_3705468 | 3649163 | A | ATGCCCAC others(4093): Show |
intron_variant | MODIFIER | NA18983.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0257 | 1 | 250 | 0.0040 | 4100 | c.112 others(4117): Show |
PIP5K1C | ENSG00000186111.11 | transcript | ENST00000335312.8 | protein_coding | 8/17 | chr19 | TogoVar | |||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(4094): Show |
upstream_gene_variant | MODIFIER | HG00609.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 8 | 0.1250 | 4101 | c.-45 others(4110): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
PNPLA7_chr9_137454952_137555402 | 137502685 | A | AGGGGGAC others(4095): Show |
intron_variant | MODIFIER | NA19070.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0085 | 1 | 82 | 0.0122 | 4102 | c.147 others(4119): Show |
PNPLA7 | ENSG00000130653.16 | transcript | ENST00000406427.6 | protein_coding | 14/34 | chr9 | TogoVar | |||||||
TWIST2_chr2_238843085_238915534 | 238870135 | C | CAAACCAC others(4095): Show |
intron_variant | MODIFIER | HG02015.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0057 | 1 | 319 | 0.0031 | 4102 | c.*35 others(4121): Show |
TWIST2 | ENSG00000233608.5 | transcript | ENST00000612363.2 | protein_coding | 1/1 | chr2 | TogoVar | |||||||
C2orf80_chr2_208160347_208195030 | 208176941 | C | CTGTATAC others(4097): Show |
intron_variant | MODIFIER | NA18944.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0202 | 1 | 233 | 0.0043 | 4104 | c.366 others(4121): Show |
C2orf80 | ENSG00000188674.11 | transcript | ENST00000341287.9 | protein_coding | 6/8 | chr2 | TogoVar | |||||||
PIEZO1_chr16_88710338_88790220 | 88731922 | A | AGAGGGCG others(4097): Show |
intron_variant | MODIFIER | NA19004.hp1 | a0026 | a0026c0121 | a0026c0121t0001 | a0026c0121t0001g0172 | 1 | 34 | 0.0294 | 4104 | c.299 others(4119): Show |
PIEZO1 | ENSG00000103335.22 | transcript | ENST00000301015.14 | protein_coding | 21/50 | chr16 | TogoVar | |||||||
TMEM242_chr6_157284025_157328519 | 157311382 | G | GAGCACTC others(4098): Show |
intron_variant | MODIFIER | HG02809.hp1 | a0001 | a0001c0001 | a0001c0001t0027 | a0001c0001t0027g0074 | 1 | 280 | 0.0036 | 4105 | c.327 others(4122): Show |
TMEM242 | ENSG00000215712.11 | transcript | ENST00000400788.9 | protein_coding | 3/3 | chr6 | TogoVar | |||||||
C2orf80_chr2_208160347_208195030 | 208176941 | C | CCGTATAC others(4099): Show |
intron_variant | MODIFIER | NA18612.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0118 | 1 | 233 | 0.0043 | 4106 | c.366 others(4123): Show |
C2orf80 | ENSG00000188674.11 | transcript | ENST00000341287.9 | protein_coding | 6/8 | chr2 | TogoVar | |||||||
GNPDA1_chr5_141995671_142018027 | 142000088 | A | ATGCTTGG others(4099): Show |
downstream_gene_variant | MODIFIER | HG01168.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0125 | 1 | 30 | 0.0333 | 4106 | c.*19 others(4117): Show |
GNPDA1 | ENSG00000113552.16 | transcript | ENST00000311337.11 | protein_coding | 582 | chr5 | TogoVar | |||||||
MORN1_chr1_2316253_2396554 | 2325140 | C | CTCCCTCC others(4099): Show |
intron_variant | MODIFIER | HG02056.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0024 | 1 | 2 | 0.5000 | 4106 | c.125 others(4123): Show |
MORN1 | ENSG00000116151.14 | transcript | ENST00000378531.8 | protein_coding | 12/13 | chr1 | TogoVar | |||||||
OR7D2_chr19_9173979_9193818 | 9175361 | A | ATAATCCC others(4099): Show |
upstream_gene_variant | MODIFIER | NA18977.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 389 | 0.0026 | 4106 | c.-38 others(4117): Show |
OR7D2 | ENSG00000188000.6 | transcript | ENST00000641288.2 | protein_coding | 3617 | chr19 | TogoVar | |||||||
DISC1_chr1_231621790_232046272 | 231799889 | T | TTCCCTCC others(4100): Show |
intron_variant | MODIFIER | HG04115.hp2 | a0004 | a0004c0013 | a0004c0013t0002 | a0004c0013t0002g0030 | 1 | 3 | 0.3333 | 4107 | c.169 others(4124): Show |
DISC1 | ENSG00000162946.24 | transcript | ENST00000439617.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
OR2T1_chr1_248398048_248413020 | 248404195 | C | CGTGTGTG others(4100): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0100 | 1 | 3 | 0.3333 | 4107 | c.-34 others(4122): Show |
OR2T1 | ENSG00000175143.5 | transcript | ENST00000642005.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
OR2T1_chr1_248398048_248413020 | 248404195 | C | CGTGTGTG others(4100): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02145.hp1 HG02451.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0002 | 8 | 10 | 0.8000 | 4107 | c.-34 others(4122): Show |
OR2T1 | ENSG00000175143.5 | transcript | ENST00000642005.1 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
PIEZO1_chr16_88710338_88790220 | 88731922 | A | AGAGGGCG others(4100): Show |
intron_variant | MODIFIER | NA21309.hp2 | a0003 | a0003c0005 | a0003c0005t0008 | a0003c0005t0008g0281 | 1 | 34 | 0.0294 | 4107 | c.299 others(4122): Show |
PIEZO1 | ENSG00000103335.22 | transcript | ENST00000301015.14 | protein_coding | 21/50 | chr16 | TogoVar | |||||||
SPAAR_chr9_35904490_35916686 | 35914283 | A | AGTGTGTG others(4100): Show |
downstream_gene_variant | MODIFIER | HG01516.hp1 HG01517.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 2 | 226 | 0.0088 | 4107 | c.*35 others(4118): Show |
SPAAR | ENSG00000235387.5 | transcript | ENST00000443779.3 | protein_coding | 2598 | chr9 | TogoVar | |||||||
ASAP2_chr2_9201812_9410678 | 9406471 | G | GTGTGTGT others(4101): Show |
downstream_gene_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0038 | 1 | 177 | 0.0056 | 4108 | c.*31 others(4119): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 794 | chr2 | TogoVar | |||||||
CLCN5_chrX_49917596_50104230 | 50057375 | G | GTCCTGGA others(4101): Show |
intron_variant | MODIFIER | HG00642.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0143 | 1 | 16 | 0.0625 | 4108 | c.164 others(4127): Show |
CLCN5 | ENSG00000171365.17 | transcript | ENST00000376091.8 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
GALNT9_chr12_132191372_132334589 | 132242699 | C | CCCCTTCC others(4101): Show |
intron_variant | MODIFIER | HG01928.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0137 | 1 | 152 | 0.0066 | 4108 | c.107 others(4127): Show |
GALNT9 | ENSG00000182870.13 | transcript | ENST00000328957.13 | protein_coding | 6/10 | chr12 | TogoVar | |||||||
OR7D2_chr19_9173979_9193818 | 9175361 | A | ATAATCCC others(4101): Show |
upstream_gene_variant | MODIFIER | NA18954.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 389 | 0.0026 | 4108 | c.-38 others(4119): Show |
OR7D2 | ENSG00000188000.6 | transcript | ENST00000641288.2 | protein_coding | 3617 | chr19 | TogoVar | |||||||
TMEM242_chr6_157284025_157328519 | 157311001 | C | CATCATAG others(4102): Show |
intron_variant | MODIFIER | NA18522.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0165 | 1 | 37 | 0.0270 | 4109 | c.327 others(4126): Show |
TMEM242 | ENSG00000215712.11 | transcript | ENST00000400788.9 | protein_coding | 3/3 | chr6 | TogoVar | |||||||
DOCK1_chr10_126900428_127457516 | 126947620 | G | GGTTGGTA others(4103): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0056 | 1 | 127 | 0.0079 | 4110 | c.47- others(4127): Show |
DOCK1 | ENSG00000150760.13 | transcript | ENST00000623213.2 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr10 | TogoVar |