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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
PRKG1_chr10_51069487_52303350 | 52109718 | ACGCCACT others(562): Show |
A | intron_variant | MODIFIER | HG02896.hp2 NA18522.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0005 | a0001c0001t0003g0029a0001c0001t0005g0031 | 2 | 64 | 0.0313 | -569 | c.936 others(19): Show |
PRKG1 | ENSG00000185532.20 | transcript | ENST00000373980.11 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
SNTG2_chr2_945849_1372613 | 1342275 | TGCTCTGT others(562): Show |
T | intron_variant | MODIFIER | NA18983.hp2 | a0012 | a0012c0019 | a0012c0019t0001 | a0012c0019t0001g0122 | 1 | 190 | 0.0053 | -569 | c.148 others(21): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
SNTG2_chr2_945849_1372613 | 1342468 | CGCACTTT others(562): Show |
C | intron_variant | MODIFIER | HG01517.hp1 | a0003 | a0003c0008 | a0003c0008t0001 | a0003c0008t0001g0190 | 1 | 190 | 0.0053 | -569 | c.148 others(21): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
SNTG2_chr2_945849_1372613 | 1342704 | CCCCCTGT others(562): Show |
C | intron_variant | MODIFIER | HG00673.hp1 NA18943.hp1 NA18961.hp2 others(2): Show |
a0001a0006 | a0001c0001a0001c0002a0006c0010 | a0001c0001t0001a0001c0002t0001a0006c0010t0001 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0002t0001g0028others(2): Show | 5 | 190 | 0.0263 | -569 | c.148 others(21): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
THBS3_chr1_155190588_155212897 | 155190614 | CGGCCTGG others(562): Show |
C | downstream_gene_variant | MODIFIER | NA19084.hp1 NA20129.hp1 homoSapiens_chm13v2.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002a0001c0001t0001g0060 | 3 | 298 | 0.0101 | -569 | c.*46 others(11): Show |
THBS3 | ENSG00000169231.13 | transcript | ENST00000368378.7 | protein_coding | 4973 | chr1 | TogoVar | ||||||
TSPAN7_chrX_38556542_38693918 | 38572624 | TCAGTTCA others(562): Show |
T | intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0076 | 1 | 223 | 0.0045 | -569 | c.81+ others(17): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | TogoVar | ||||||
CA5A_chr16_87883013_87941529 | 87898838 | GATTCTCC others(561): Show |
G | intron_variant | MODIFIER | HG00438.hp2 NA18955.hp2 NA19074.hp2 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0148a0001c0002t0002g0172a0001c0002t0002g0211 | 3 | 400 | 0.0075 | -568 | c.618 others(17): Show |
CA5A | ENSG00000174990.8 | transcript | ENST00000649794.3 | protein_coding | 5/6 | chr16 | TogoVar | ||||||
DCC_chr18_52335197_53540899 | 53085988 | TCTCCTTC others(561): Show |
T | intron_variant | MODIFIER | HG00738.hp2 HG01106.hp2 HG02486.hp2 others(2): Show |
a0002a0009 | a0002c0001a0002c0004a0002c0013others(1): Show | a0002c0001t0018a0002c0004t0003a0002c0013t0001others(1): Show | a0002c0001t0018g0034a0002c0004t0003g0012a0002c0004t0003g0023others(2): Show | 5 | 114 | 0.0439 | -568 | c.126 others(21): Show |
DCC | ENSG00000187323.13 | transcript | ENST00000442544.7 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
FAT1_chr4_186582794_186728856 | 186626223 | AGAATGAA others(561): Show |
A | intron_variant | MODIFIER | NA18967.hp2 | a0030 | a0030c0025 | a0030c0025t0034 | a0030c0025t0034g0291 | 1 | 338 | 0.0030 | -568 | c.481 others(19): Show |
FAT1 | ENSG00000083857.15 | transcript | ENST00000441802.7 | protein_coding | 9/26 | chr4 | TogoVar | ||||||
FKRP_chr19_46741057_46763575 | 46754258 | GAACTCCT others(561): Show |
G | intron_variant | MODIFIER | HG02258.hp2 HG03130.hp2 |
a0001 | a0001c0003 | a0001c0003t0007 | a0001c0003t0007g0037 | 2 | 430 | 0.0047 | -568 | c.-39 others(16): Show |
FKRP | ENSG00000181027.11 | transcript | ENST00000318584.10 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ISY1_chr3_129122415_129166063 | 129155359 | TAATATTT others(561): Show |
T | intron_variant | MODIFIER | HG04228.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0066 | 1 | 366 | 0.0027 | -568 | c.187 others(16): Show |
ISY1 | ENSG00000240682.10 | transcript | ENST00000393295.8 | protein_coding | 5/10 | chr3 | TogoVar | ||||||
NEU4_chr2_241804193_241822413 | 241819462 | CTCATGCG others(561): Show |
C | downstream_gene_variant | MODIFIER | NA19066.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0045 | 1 | 319 | 0.0031 | -568 | c.*24 others(11): Show |
NEU4 | ENSG00000204099.12 | transcript | ENST00000407683.6 | protein_coding | 2050 | chr2 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149500 | CTAATCCC others(561): Show |
C | intron_variant | MODIFIER | NA18991.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0090 | 1 | 294 | 0.0034 | -568 | c.901 others(15): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | chr12 | TogoVar | ||||||
PACS1_chr11_66065272_66249744 | 66116631 | GCCTGTAA others(561): Show |
G | intron_variant | MODIFIER | HG02615.hp1 HG03579.hp1 NA18522.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0311a0001c0001t0005g0206a0001c0001t0005g0207 | 3 | 322 | 0.0093 | -568 | c.356 others(19): Show |
PACS1 | ENSG00000175115.13 | transcript | ENST00000320580.9 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 745127 | GCCGTGGA others(561): Show |
G | intron_variant | MODIFIER | HG01928.hp1 HG02004.hp2 HG02165.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0014a0002c0002t0003a0002c0002t0048 | a0001c0001t0014g0025a0002c0002t0003g0039a0002c0002t0003g0070others(1): Show | 4 | 366 | 0.0109 | -568 | c.462 others(16): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 745610 | CCCGGGGG others(561): Show |
C | intron_variant | MODIFIER | HG00609.hp1 HG02040.hp1 NA18980.hp1 |
a0001a0002 | a0001c0003a0002c0002 | a0001c0003t0005a0002c0002t0003 | a0001c0003t0005g0138a0002c0002t0003g0048a0002c0002t0003g0068 | 3 | 366 | 0.0082 | -568 | c.462 others(16): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 745952 | CCCCGGGG others(561): Show |
C | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(24): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0156a0001c0001t0002g0146a0001c0001t0002g0149others(24): Show | 27 | 366 | 0.0738 | -568 | c.462 others(17): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 746094 | TCCGTGGA others(561): Show |
T | intron_variant | MODIFIER | HG00741.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0348 | 1 | 366 | 0.0027 | -568 | c.462 others(17): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PLD5_chr1_242077986_242529697 | 242393766 | AAGTATTT others(561): Show |
A | intron_variant | MODIFIER | NA19003.hp2 | a0001 | a0001c0001 | a0001c0001t0018 | a0001c0001t0018g0015 | 1 | 188 | 0.0053 | -568 | c.190 others(19): Show |
PLD5 | ENSG00000180287.17 | transcript | ENST00000536534.7 | protein_coding | 1/9 | chr1 | TogoVar | ||||||
PTGR1_chr9_111557567_111604647 | 111571017 | GCTAGAAG others(561): Show |
G | intron_variant | MODIFIER | HG00280.hp2 HG00544.hp1 HG00558.hp1 others(65): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0280a0001c0001t0002g0029a0001c0001t0002g0031others(60): Show | 68 | 408 | 0.1667 | -568 | c.761 others(16): Show |
PTGR1 | ENSG00000106853.20 | transcript | ENST00000407693.7 | protein_coding | 8/9 | chr9 | TogoVar | ||||||
SLC12A7_chr5_1045384_1117063 | 1048087 | GGGGTGTG others(561): Show |
G | downstream_gene_variant | MODIFIER | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(14): Show |
a0001a0002a0003 | a0001c0003a0001c0013a0001c0014others(3): Show | a0001c0003t0003a0001c0003t0017a0001c0013t0003others(5): Show | a0001c0003t0003g0002a0001c0003t0003g0004a0001c0003t0003g0005others(14): Show | 17 | 118 | 0.1441 | -568 | c.*37 others(11): Show |
SLC12A7 | ENSG00000113504.21 | transcript | ENST00000264930.10 | protein_coding | 2296 | chr5 | TogoVar | ||||||
ADARB2_chr10_1172313_1742525 | 1235661 | CCCCTCTC others(560): Show |
C | intron_variant | MODIFIER | HG02145.hp2 NA19011.hp2 |
a0002 | a0002c0002 | a0002c0002t0004a0002c0002t0008 | a0002c0002t0004g0088a0002c0002t0008g0042 | 2 | 106 | 0.0189 | -567 | c.136 others(19): Show |
ADARB2 | ENSG00000185736.16 | transcript | ENST00000381312.6 | protein_coding | 5/9 | chr10 | TogoVar | ||||||
ADARB2_chr10_1172313_1742525 | 1235669 | CCTCCCGG others(560): Show |
C | intron_variant | MODIFIER | NA20805.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0067 | 1 | 106 | 0.0094 | -567 | c.136 others(19): Show |
ADARB2 | ENSG00000185736.16 | transcript | ENST00000381312.6 | protein_coding | 5/9 | chr10 | TogoVar | ||||||
EHHADH_chr3_185185624_185259049 | 185230540 | CTAAACAA others(560): Show |
C | intron_variant | MODIFIER | HG02818.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0014 | 1 | 348 | 0.0029 | -567 | c.352 others(16): Show |
EHHADH | ENSG00000113790.11 | transcript | ENST00000231887.8 | protein_coding | 3/6 | chr3 | TogoVar | ||||||
EHHADH_chr3_185185624_185259049 | 185230658 | GTATGATT others(560): Show |
G | intron_variant | MODIFIER | HG01074.hp1 HG01074.hp2 HG01109.hp2 others(32): Show |
a0001a0002a0004others(2): Show | a0001c0001a0002c0002a0002c0004others(4): Show | a0001c0001t0003a0002c0002t0002a0002c0002t0007others(7): Show | a0001c0001t0003g0291a0001c0001t0003g0292a0001c0001t0003g0293others(32): Show | 35 | 348 | 0.1006 | -567 | c.352 others(17): Show |
EHHADH | ENSG00000113790.11 | transcript | ENST00000231887.8 | protein_coding | 3/6 | chr3 | TogoVar | ||||||
EHHADH_chr3_185185624_185259049 | 185231107 | ATAAACAA others(560): Show |
A | intron_variant | MODIFIER | HG00140.hp1 HG00597.hp2 HG00741.hp2 others(29): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002 | a0001c0001t0001g0313a0001c0001t0001g0332a0002c0002t0002g0001others(25): Show | 32 | 348 | 0.0920 | -567 | c.352 others(17): Show |
EHHADH | ENSG00000113790.11 | transcript | ENST00000231887.8 | protein_coding | 3/6 | chr3 | TogoVar | ||||||
EVA1C_chr21_32407706_32520387 | 32470884 | GAGTAGCT others(560): Show |
G | intron_variant | MODIFIER | NA20805.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0259 | 1 | 346 | 0.0029 | -567 | c.634 others(17): Show |
EVA1C | ENSG00000166979.13 | transcript | ENST00000300255.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | |||||
FOXN3_chr14_89151177_89422233 | 89362104 | AGCACCAC others(560): Show |
A | intron_variant | MODIFIER | NA18964.hp1 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0033 | 1 | 230 | 0.0044 | -567 | c.544 others(19): Show |
FOXN3 | ENSG00000053254.16 | transcript | ENST00000557258.6 | protein_coding | 2/5 | chr14 | TogoVar | ||||||
LYPD8_chr1_248734415_248760759 | 248746588 | CGCACGGC others(560): Show |
C | intron_variant | MODIFIER | HG01934.hp2 HG03579.hp1 NA18950.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006 | a0001c0001t0001g0010a0001c0001t0001g0099a0001c0001t0001g0216others(2): Show | 7 | 374 | 0.0187 | -567 | c.337 others(17): Show |
LYPD8 | ENSG00000259823.6 | transcript | ENST00000590317.4 | protein_coding | 5/6 | chr1 | TogoVar | ||||||
NOC4L_chr12_132139457_132157468 | 132149529 | ACTCACAC others(560): Show |
A | intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0212 | 1 | 294 | 0.0034 | -567 | c.901 others(15): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
NOC4L_chr12_132139457_132157468 | 132149573 | ACTCACAC others(560): Show |
A | intron_variant | MODIFIER | HG01081.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0185 | 1 | 294 | 0.0034 | -567 | c.901 others(15): Show |
NOC4L | ENSG00000184967.7 | transcript | ENST00000330579.6 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 746009 | CCCGGGGG others(560): Show |
C | intron_variant | MODIFIER | HG02145.hp2 NA19240.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0057 | a0001c0001t0002g0329a0002c0002t0057g0330 | 2 | 366 | 0.0055 | -567 | c.462 others(17): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PCGF3_chr4_700832_775089 | 746465 | CCCGGGGT others(560): Show |
C | intron_variant | MODIFIER | HG00609.hp1 HG01928.hp1 HG02074.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0035a0002c0002t0003others(1): Show | a0001c0001t0003g0043a0001c0001t0035g0046a0002c0002t0003g0039others(4): Show | 7 | 366 | 0.0191 | -567 | c.462 others(17): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
PRDM15_chr21_41793225_41884344 | 41844565 | CACACACA others(560): Show |
C | intron_variant | MODIFIER | HG03927.hp1 HG04115.hp2 |
a0001 | a0001c0001a0001c0019 | a0001c0001t0014a0001c0019t0002 | a0001c0001t0014g0155a0001c0019t0002g0162 | 2 | 406 | 0.0049 | -567 | c.640 others(17): Show |
PRDM15 | ENSG00000141956.14 | transcript | ENST00000398548.6 | protein_coding | 6/23 | chr21 | TogoVar | ||||||
SNTG2_chr2_945849_1372613 | 1344624 | GGCACTTT others(560): Show |
G | intron_variant | MODIFIER | HG01891.hp2 HG03453.hp2 |
a0001a0007 | a0001c0002a0007c0016 | a0001c0002t0001a0007c0016t0001 | a0001c0002t0001g0041a0007c0016t0001g0005 | 2 | 190 | 0.0105 | -567 | c.148 others(21): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
SOX5_chr12_23524504_23954670 | 23786587 | TTTGTAGG others(560): Show |
T | intron_variant | MODIFIER | HG00597.hp2 HG00609.hp1 HG00735.hp1 others(32): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(28): Show | a0001c0001t0001g0108a0001c0001t0001g0114a0001c0001t0002g0200others(32): Show | 35 | 212 | 0.1651 | -567 | c.482 others(19): Show |
SOX5 | ENSG00000134532.20 | transcript | ENST00000451604.7 | protein_coding | 3/14 | chr12 | TogoVar | ||||||
SP140L_chr2_230322193_230408732 | 230343095 | CAACTTTT others(560): Show |
C | intron_variant | MODIFIER | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(37): Show |
a0002a0004a0005others(3): Show | a0002c0024a0002c0025a0004c0005others(6): Show | a0002c0024t0001a0002c0025t0001a0004c0005t0001others(6): Show | a0002c0024t0001g0081a0002c0025t0001g0085a0004c0005t0001g0079others(37): Show | 40 | 336 | 0.1191 | -567 | c.107 others(19): Show |
SP140L | ENSG00000185404.17 | transcript | ENST00000415673.7 | protein_coding | 2/18 | chr2 | TogoVar | ||||||
C2CD3_chr11_74007718_74176002 | 74050711 | GTTTGGAC others(559): Show |
G | intron_variant | MODIFIER | HG02145.hp2 HG02717.hp1 HG02965.hp1 others(7): Show |
a0007a0011a0027 | a0007c0009a0011c0018a0027c0047 | a0007c0009t0002a0011c0018t0001a0027c0047t0002 | a0007c0009t0002g0310a0007c0009t0002g0312a0007c0009t0002g0313others(7): Show | 10 | 318 | 0.0315 | -566 | c.515 others(19): Show |
C2CD3 | ENSG00000168014.18 | transcript | ENST00000334126.12 | protein_coding | 26/32 | chr11 | TogoVar | ||||||
CPAMD8_chr19_16887951_17031810 | 16976274 | GAGACCAG others(559): Show |
G | intron_variant | MODIFIER | HG01891.hp2 HG03471.hp1 |
a0100a0122 | a0100c0068a0122c0162 | a0100c0068t0002a0122c0162t0001 | a0100c0068t0002g0159a0122c0162t0001g0019 | 2 | 278 | 0.0072 | -566 | c.175 others(17): Show |
CPAMD8 | ENSG00000160111.15 | transcript | ENST00000443236.7 | protein_coding | 15/41 | chr19 | TogoVar | ||||||
EHMT1_chr9_137614005_137841127 | 137818862 | GCGCCGTG others(559): Show |
G | intron_variant | MODIFIER | HG01257.hp1 HG02165.hp1 HG02258.hp2 others(3): Show |
a0001 | a0001c0001a0001c0011 | a0001c0001t0001a0001c0011t0001 | a0001c0001t0001g0087a0001c0001t0001g0112a0001c0001t0001g0115others(3): Show | 6 | 170 | 0.0353 | -566 | c.354 others(18): Show |
EHMT1 | ENSG00000181090.21 | transcript | ENST00000460843.6 | protein_coding | 25/26 | chr9 | TogoVar | ||||||
GRTP1_chr13_113319163_113369130 | 113346354 | AGGAGGAC others(559): Show |
A | intron_variant | MODIFIER | HG00621.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0197 | 1 | 288 | 0.0035 | -566 | c.466 others(17): Show |
GRTP1 | ENSG00000139835.14 | transcript | ENST00000375431.9 | protein_coding | 4/7 | chr13 | TogoVar | ||||||
GRTP1_chr13_113319163_113369130 | 113346471 | CGGGAGGA others(559): Show |
C | intron_variant | MODIFIER | HG02451.hp2 HG03579.hp2 |
a0001a0006 | a0001c0001a0006c0006 | a0001c0001t0003a0006c0006t0005 | a0001c0001t0003g0266a0006c0006t0005g0253 | 2 | 288 | 0.0069 | -566 | c.466 others(17): Show |
GRTP1 | ENSG00000139835.14 | transcript | ENST00000375431.9 | protein_coding | 4/7 | chr13 | TogoVar | ||||||
IQCH_chr15_67249786_67506804 | 67391144 | AGCCAGGA others(559): Show |
A | intron_variant | MODIFIER | HG00558.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 | 1 | 276 | 0.0036 | -566 | c.163 others(19): Show |
IQCH | ENSG00000103599.20 | transcript | ENST00000335894.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
PLD5_chr1_242077986_242529697 | 242393746 | ATGTGTGT others(559): Show |
A | intron_variant | MODIFIER | HG03688.hp2 NA19066.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0003 | a0001c0001t0002g0005a0001c0002t0003g0147 | 2 | 188 | 0.0106 | -566 | c.190 others(19): Show |
PLD5 | ENSG00000180287.17 | transcript | ENST00000536534.7 | protein_coding | 1/9 | chr1 | TogoVar | ||||||
PRRX2_chr9_129660647_129727674 | 129662049 | ATGAGCCA others(559): Show |
A | upstream_gene_variant | MODIFIER | HG00558.hp1 HG00621.hp1 HG00621.hp2 others(51): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0003a0001c0001t0001g0161a0001c0001t0001g0164others(50): Show | 54 | 358 | 0.1508 | -566 | c.-38 others(11): Show |
PRRX2 | ENSG00000167157.11 | transcript | ENST00000372469.6 | protein_coding | 3597 | chr9 | TogoVar | ||||||
RNF223_chr1_1065967_1079306 | 1076151 | TGGGGACT others(559): Show |
T | upstream_gene_variant | MODIFIER | HG01884.hp2 HG02109.hp2 HG02572.hp2 others(4): Show |
a0002 | a0002c0002 | a0002c0002t0006 | a0002c0002t0006g0007 | 7 | 324 | 0.0216 | -566 | c.-27 others(11): Show |
RNF223 | ENSG00000237330.3 | transcript | ENST00000453464.3 | protein_coding | 1846 | chr1 | TogoVar | ||||||
TTLL8_chr22_50013575_50063298 | 50028645 | CCCCATCA others(559): Show |
C | intron_variant | MODIFIER | NA20129.hp1 | a0004 | a0004c0004 | a0004c0004t0001 | a0004c0004t0001g0134 | 1 | 224 | 0.0045 | -566 | c.225 others(19): Show |
TTLL8 | ENSG00000138892.12 | transcript | ENST00000433387.2 | protein_coding | 13/13 | chr22 | TogoVar | ||||||
VIPR2_chr7_159023175_159149867 | 159087194 | TGGCTTCC others(559): Show |
T | intron_variant | MODIFIER | NA19057.hp1 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0128 | 1 | 336 | 0.0030 | -566 | c.357 others(19): Show |
VIPR2 | ENSG00000106018.14 | transcript | ENST00000262178.7 | protein_coding | 4/12 | chr7 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1889453 | GGGTGAGG others(558): Show |
G | intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0141 | a0001c0141t0007 | a0001c0141t0007g0099 | 1 | 363 | 0.0028 | -565 | c.118 others(19): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
BANK1_chr4_101785730_102079812 | 101866629 | TAGGAATA others(558): Show |
T | intron_variant | MODIFIER | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(108): Show |
a0001a0003a0004others(2): Show | a0001c0001a0001c0002a0001c0018others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(14): Show | a0001c0001t0001g0034a0001c0001t0001g0066a0001c0001t0001g0090others(108): Show | 111 | 284 | 0.3909 | -565 | c.764 others(17): Show |
BANK1 | ENSG00000153064.12 | transcript | ENST00000322953.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr4 | TogoVar |