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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SGTA_chr19_2749715_2788273 | 2773439 | CGGCAGGG others(526): Show |
C | intron_variant | MODIFIER | HG00438.hp1 HG01891.hp1 HG02622.hp2 others(5): Show |
a0001 | a0001c0003 | a0001c0003t0003a0001c0003t0004 | a0001c0003t0003g0022 a0001c0003t0003g0063 a0001c0003t0003g0064 others(3): Show |
8 | 385 | 0.0208 | -533 | c.-23 others(17): Show |
SGTA | ENSG00000104969.11 | transcript | ENST00000221566.7 | protein_coding | 1/11 | chr19 | TogoVar | |||||||
TAFA5_chr22_48484553_48756932 | 48667960 | ACCGCGTC others(526): Show |
A | intron_variant | MODIFIER | HG01496.hp2 HG02615.hp1 HG02647.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0015 | a0001c0001t0002g0046 a0001c0001t0002g0075 a0001c0001t0002g0193 others(2): Show |
5 | 255 | 0.0196 | -533 | c.262 others(19): Show |
TAFA5 | ENSG00000219438.9 | transcript | ENST00000402357.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
TNK2_chr3_195858364_195913551 | 195874801 | TCCCCTCG others(526): Show |
T | intron_variant | MODIFIER | HG00323.hp2 HG01361.hp2 HG01891.hp1 others(33): Show |
a0001a0002a0006others(2): Show | a0001c0001a0001c0002a0001c0013others(4): Show | a0001c0001t0001a0001c0001t0007a0001c0002t0001others(5): Show | a0001c0001t0001g0003 a0001c0001t0001g0113 a0001c0001t0001g0114 others(29): Show |
36 | 368 | 0.0978 | -533 | c.125 others(19): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | TogoVar | |||||||
TPO_chr2_1408463_1548673 | 1444635 | TGGGGCAG others(526): Show |
T | intron_variant | MODIFIER | HG00597.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0015 | 1 | 87 | 0.0115 | -533 | c.482 others(17): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
B4GALNT4_chr11_364499_387117 | 384901 | ACACAGCT others(525): Show |
A | downstream_gene_variant | MODIFIER | HG00438.hp2 NA19007.hp2 NA19012.hp2 others(1): Show |
a0002 | a0002c0002a0002c0008 | a0002c0002t0001a0002c0008t0001 | a0002c0002t0001g0069 a0002c0002t0001g0075 a0002c0002t0001g0083 others(1): Show |
4 | 112 | 0.0357 | -532 | c.*31 others(11): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 2785 | chr11 | TogoVar | |||||||
C1orf174_chr1_3884133_3905272 | 3888429 | CCCAATGG others(525): Show |
C | downstream_gene_variant | MODIFIER | NA18522.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0133 | 1 | 438 | 0.0023 | -532 | c.*99 others(10): Show |
C1orf174 | ENSG00000198912.12 | transcript | ENST00000361605.4 | protein_coding | 703 | chr1 | TogoVar | |||||||
CTDP1_chr18_79674803_79759503 | 79745262 | TGCGTCCC others(525): Show |
T | intron_variant | MODIFIER | NA19030.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0092 | 1 | 339 | 0.0029 | -532 | c.274 others(19): Show |
CTDP1 | ENSG00000060069.18 | transcript | ENST00000613122.5 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
DFFB_chr1_3852476_3890429 | 3888429 | CCCAATGG others(525): Show |
C | downstream_gene_variant | MODIFIER | NA18522.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0265 | 1 | 402 | 0.0025 | -532 | c.*46 others(11): Show |
DFFB | ENSG00000169598.17 | transcript | ENST00000378209.8 | protein_coding | 3001 | chr1 | TogoVar | |||||||
DPH7_chr9_137549444_137583925 | 137567492 | TGTCTGTG others(525): Show |
T | intron_variant | MODIFIER | HG00621.hp1 | a0001 | a0001c0011 | a0001c0011t0001 | a0001c0011t0001g0314 | 1 | 333 | 0.0030 | -532 | c.641 others(17): Show |
DPH7 | ENSG00000148399.13 | transcript | ENST00000277540.7 | protein_coding | 5/8 | chr9 | TogoVar | |||||||
NKD2_chr5_1003802_1043943 | 1024308 | TGTGGGCG others(525): Show |
T | intron_variant | MODIFIER | HG02145.hp2 HG02895.hp2 HG03453.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0186 a0001c0001t0003g0011 a0001c0001t0003g0105 |
4 | 303 | 0.0132 | -532 | c.142 others(17): Show |
NKD2 | ENSG00000145506.14 | transcript | ENST00000296849.10 | protein_coding | 3/9 | chr5 | TogoVar | |||||||
NXN_chr17_794310_984776 | 949052 | TGCCTCCT others(525): Show |
T | intron_variant | MODIFIER | HG00735.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0157 | 1 | 222 | 0.0045 | -532 | c.360 others(19): Show |
NXN | ENSG00000167693.17 | transcript | ENST00000336868.8 | protein_coding | 1/7 | chr17 | TogoVar | |||||||
OR6B3_chr2_240039571_240058521 | 240042047 | CGAAGGGC others(525): Show |
C | downstream_gene_variant | MODIFIER | HG03491.hp1 | a0003 | a0003c0004 | a0003c0004t0003 | a0003c0004t0003g0003 | 1 | 442 | 0.0023 | -532 | c.*24 others(11): Show |
OR6B3 | ENSG00000178586.7 | transcript | ENST00000641019.2 | protein_coding | 2523 | chr2 | TogoVar | |||||||
OR6B3_chr2_240039571_240058521 | 240042195 | CGTGGGTG others(525): Show |
C | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(118): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0011others(2): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0011others(4): Show | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(26): Show |
121 | 442 | 0.2738 | -532 | c.*23 others(11): Show |
OR6B3 | ENSG00000178586.7 | transcript | ENST00000641019.2 | protein_coding | 2375 | chr2 | TogoVar | |||||||
PLEKHG4B_chr5_87168_194966 | 165971 | CTCTGACG others(525): Show |
C | intron_variant | MODIFIER | HG02922.hp2 | a0006 | a0006c0071 | a0006c0071t0018 | a0006c0071t0018g0202 | 1 | 208 | 0.0048 | -532 | c.347 others(19): Show |
PLEKHG4B | ENSG00000153404.15 | transcript | ENST00000637938.2 | protein_coding | 13/19 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
SAMD11_chr1_918923_949574 | 934217 | CCGTTACA others(525): Show |
C | intron_variant | MODIFIER | HG01891.hp1 HG02647.hp2 HG02809.hp1 others(3): Show |
a0001a0005 | a0001c0001a0001c0004a0005c0012 | a0001c0001t0001a0001c0004t0001a0005c0012t0001 | a0001c0001t0001g0138 a0001c0004t0001g0141 a0005c0012t0001g0009 others(1): Show |
6 | 320 | 0.0188 | -532 | c.843 others(16): Show |
SAMD11 | ENSG00000187634.13 | transcript | ENST00000616016.5 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
SLC66A2_chr18_79897420_79956653 | 79920037 | GAGGAGAG others(525): Show |
G | intron_variant | MODIFIER | HG01256.hp2 HG01515.hp2 HG01517.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0011 | a0001c0001t0005g0025 a0001c0001t0005g0219 a0001c0001t0011g0011 |
4 | 348 | 0.0115 | -532 | c.392 others(16): Show |
SLC66A2 | ENSG00000122490.19 | transcript | ENST00000397778.7 | protein_coding | 4/5 | chr18 | TogoVar | |||||||
SULT4A1_chr22_43819509_43867513 | 43834348 | AGCTTCCC others(525): Show |
A | intron_variant | MODIFIER | HG00099.hp1 HG01496.hp1 HG02895.hp2 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0006 | a0001c0001t0003g0008 a0001c0001t0006g0132 |
3 | 383 | 0.0078 | -532 | c.509 others(16): Show |
SULT4A1 | ENSG00000130540.14 | transcript | ENST00000330884.9 | protein_coding | 4/6 | chr22 | TogoVar | |||||||
TNK2_chr3_195858364_195913551 | 195874713 | CTCCCTCG others(525): Show |
C | intron_variant | MODIFIER | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(24): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(7): Show | a0001c0001t0001g0064 a0001c0001t0001g0252 a0001c0001t0001g0253 others(21): Show |
27 | 318 | 0.0849 | -532 | c.125 others(19): Show |
TNK2 | ENSG00000061938.21 | transcript | ENST00000672887.2 | protein_coding | 9/15 | chr3 | TogoVar | |||||||
ZFAT_chr8_134472788_134718031 | 134498639 | TTGCTGGT others(525): Show |
T | intron_variant | MODIFIER | HG01081.hp1 HG01175.hp2 HG01257.hp2 others(13): Show |
a0001 | a0001c0001a0001c0003a0001c0018 | a0001c0001t0001a0001c0003t0001a0001c0003t0002others(1): Show | a0001c0001t0001g0001 a0001c0003t0001g0031 a0001c0003t0001g0035 others(12): Show |
16 | 272 | 0.0588 | -532 | c.349 others(21): Show |
ZFAT | ENSG00000066827.16 | transcript | ENST00000377838.8 | protein_coding | 15/15 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144531250 | CGAGCAGC others(524): Show |
C | intron_variant | MODIFIER | HG03195.hp1 HG03209.hp1 HG03453.hp1 |
a0001 | a0001c0001a0001c0014 | a0001c0001t0003a0001c0001t0021a0001c0014t0007 | a0001c0001t0003g0020 a0001c0001t0021g0057 a0001c0014t0007g0239 |
3 | 214 | 0.0140 | -531 | c.298 others(17): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144531505 | GGGCTAGA others(524): Show |
G | intron_variant | MODIFIER | HG02451.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0017 | 1 | 230 | 0.0043 | -531 | c.298 others(17): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1874722 | TGTGTAAG others(524): Show |
T | intron_variant | MODIFIER | HG01361.hp2 | a0002 | a0002c0128 | a0002c0128t0001 | a0002c0128t0001g0061 | 1 | 362 | 0.0028 | -531 | c.680 others(17): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
C1orf87_chr1_59985394_60078770 | 60022254 | CAGAGTTC others(524): Show |
C | intron_variant | MODIFIER | NA18984.hp1 NA18993.hp2 NA19079.hp2 |
a0001 | a0001c0009 | a0001c0009t0001 | a0001c0009t0001g0003 | 3 | 380 | 0.0079 | -531 | c.112 others(19): Show |
C1orf87 | ENSG00000162598.13 | transcript | ENST00000371201.3 | protein_coding | 8/11 | chr1 | TogoVar | |||||||
C8orf82_chr8_144520733_144534111 | 144531250 | CGAGCAGC others(524): Show |
C | upstream_gene_variant | MODIFIER | HG02258.hp1 HG03195.hp1 HG03209.hp1 others(1): Show |
a0001 | a0001c0003 | a0001c0003t0004a0001c0003t0009 | a0001c0003t0004g0053 a0001c0003t0009g0025 a0001c0003t0009g0062 |
4 | 348 | 0.0115 | -531 | c.-28 others(11): Show |
C8orf82 | ENSG00000213563.7 | transcript | ENST00000524821.6 | protein_coding | 2140 | chr8 | TogoVar | |||||||
C8orf82_chr8_144520733_144534111 | 144531505 | GGGCTAGA others(524): Show |
G | upstream_gene_variant | MODIFIER | HG02451.hp2 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0049 | 1 | 382 | 0.0026 | -531 | c.-31 others(11): Show |
C8orf82 | ENSG00000213563.7 | transcript | ENST00000524821.6 | protein_coding | 2395 | chr8 | TogoVar | |||||||
CAMK1D_chr10_12344547_12840545 | 12775589 | AGGTGAGA others(524): Show |
A | intron_variant | MODIFIER | HG01891.hp1 NA20300.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0104 | a0001c0001t0001g0191 a0001c0001t0104g0089 |
2 | 214 | 0.0093 | -531 | c.565 others(17): Show |
CAMK1D | ENSG00000183049.14 | transcript | ENST00000619168.5 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
COPS4_chr4_83030183_83080818 | 83063272 | TGGTAGTC others(524): Show |
T | intron_variant | MODIFIER | HG02647.hp1 HG02818.hp1 HG03486.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0074 a0001c0001t0001g0079 a0001c0001t0001g0102 |
3 | 370 | 0.0081 | -531 | c.886 others(14): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
LRRC24_chr8_144517388_144532033 | 144531250 | CGAGCAGC others(524): Show |
C | upstream_gene_variant | MODIFIER | HG02258.hp1 HG03209.hp1 HG03453.hp2 |
a0004 | a0004c0006 | a0004c0006t0001 | a0004c0006t0001g0014 | 3 | 351 | 0.0085 | -531 | c.-48 others(11): Show |
LRRC24 | ENSG00000254402.7 | transcript | ENST00000529415.7 | protein_coding | 4218 | chr8 | TogoVar | |||||||
MTA1_chr14_105414827_105475729 | 105459164 | CCCTAGGG others(524): Show |
C | intron_variant | MODIFIER | HG04204.hp2 | a0005 | a0005c0005 | a0005c0005t0001 | a0005c0005t0001g0143 | 1 | 44 | 0.0227 | -531 | c.653 others(15): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
MTA1_chr14_105414827_105475729 | 105459536 | CTGGGGGC others(524): Show |
C | intron_variant | MODIFIER | HG01975.hp2 NA19064.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0192 a0001c0001t0001g0223 |
2 | 302 | 0.0066 | -531 | c.654 others(15): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
MUC17_chr7_101015081_101063859 | 101041440 | CTAACAAA others(524): Show |
C | conservative_inframe_deletion | MODERATE | NA18982.hp1 | a0052 | a0052c0033 | a0052c0033t0003 | a0052c0033t0003g0136 | 1 | 364 | 0.0027 | -531 | c.100 others(11): Show |
p.Ser others(15): Show |
MUC17 | ENSG00000169876.14 | transcript | ENST00000306151.9 | protein_coding | 3/13 | 10091/14352 | 10036/13482 | 3346/4493 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||
NOS1AP_chr1_162064691_162375475 | 162260958 | CCTCAAAG others(524): Show |
C | intron_variant | MODIFIER | HG00544.hp2 HG00735.hp1 HG01169.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(2): Show | a0001c0001t0001g0141 a0001c0001t0002g0067 a0001c0002t0001g0022 others(4): Show |
7 | 139 | 0.0504 | -531 | c.178 others(19): Show |
NOS1AP | ENSG00000198929.13 | transcript | ENST00000361897.10 | protein_coding | 2/9 | chr1 | TogoVar | |||||||
VPS53_chr17_503668_719839 | 618462 | CACTAATA others(524): Show |
C | intron_variant | MODIFIER | HG03516.hp2 | a0001 | a0001c0002 | a0001c0002t0075 | a0001c0002t0075g0041 | 1 | 230 | 0.0043 | -531 | c.111 others(19): Show |
VPS53 | ENSG00000141252.21 | transcript | ENST00000437048.7 | protein_coding | 11/21 | chr17 | TogoVar | |||||||
BRF1_chr14_105204286_105306001 | 105275918 | TGAGAGGC others(523): Show |
T | intron_variant | MODIFIER | HG02630.hp2 NA18906.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005 a0001c0001t0001g0006 |
2 | 64 | 0.0313 | -530 | c.266 others(17): Show |
BRF1 | ENSG00000185024.18 | transcript | ENST00000547530.7 | protein_coding | 2/17 | chr14 | TogoVar | |||||||
CDC34_chr19_526760_547087 | 540223 | GTGGCCAG others(523): Show |
G | intron_variant | MODIFIER | HG03239.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0086 | 1 | 301 | 0.0033 | -530 | c.498 others(16): Show |
CDC34 | ENSG00000099804.9 | transcript | ENST00000215574.9 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
DDX51_chr12_132131594_132149319 | 132134883 | CGCTCCTC others(523): Show |
C | downstream_gene_variant | MODIFIER | HG03139.hp2 | a0011 | a0011c0015 | a0011c0015t0014 | a0011c0015t0014g0031 | 1 | 322 | 0.0031 | -530 | c.*38 others(11): Show |
DDX51 | ENSG00000185163.10 | transcript | ENST00000397333.4 | protein_coding | 1710 | chr12 | TogoVar | |||||||
DHRSX_chrX_2214506_2505976 | 2277749 | AGAGGGAG others(523): Show |
A | intron_variant | MODIFIER | HG01261.hp1 | a0003 | a0003c0003 | a0003c0003t0013 | a0003c0003t0013g0002 | 1 | 44 | 0.0227 | -530 | c.389 others(19): Show |
DHRSX | ENSG00000169084.15 | transcript | ENST00000334651.11 | protein_coding | 4/6 | chrX | TogoVar | |||||||
DPH7_chr9_137549444_137583925 | 137565338 | TGTCTGTG others(523): Show |
T | intron_variant | MODIFIER | HG02155.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0088 | 1 | 337 | 0.0030 | -530 | c.641 others(15): Show |
DPH7 | ENSG00000148399.13 | transcript | ENST00000277540.7 | protein_coding | 5/8 | chr9 | TogoVar | |||||||
DPH7_chr9_137549444_137583925 | 137567048 | ACTCTGTC others(523): Show |
A | intron_variant | MODIFIER | NA18975.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0185 | 1 | 299 | 0.0033 | -530 | c.641 others(17): Show |
DPH7 | ENSG00000148399.13 | transcript | ENST00000277540.7 | protein_coding | 5/8 | chr9 | TogoVar | |||||||
GZMM_chr19_539053_554922 | 540223 | GTGGCCAG others(523): Show |
G | upstream_gene_variant | MODIFIER | HG03239.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0052 | 1 | 366 | 0.0027 | -530 | c.-38 others(11): Show |
GZMM | ENSG00000197540.8 | transcript | ENST00000264553.6 | protein_coding | 3829 | chr19 | TogoVar | |||||||
MYOM2_chr8_2040046_2150456 | 2085546 | CACTGTCA others(523): Show |
C | intron_variant | MODIFIER | HG03704.hp1 | a0002 | a0002c0124 | a0002c0124t0002 | a0002c0124t0002g0255 | 1 | 351 | 0.0028 | -530 | c.164 others(17): Show |
MYOM2 | ENSG00000036448.10 | transcript | ENST00000262113.9 | protein_coding | 14/36 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
P2RX5_chr17_3668227_3701155 | 3686523 | CAGAACAG others(523): Show |
C | intron_variant | MODIFIER | NA19087.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0183 | 1 | 331 | 0.0030 | -530 | c.981 others(16): Show |
P2RX5 | ENSG00000083454.23 | transcript | ENST00000225328.10 | protein_coding | 9/11 | chr17 | TogoVar | |||||||
PCGF3_chr4_700832_775089 | 759195 | CGGGTCTT others(523): Show |
C | intron_variant | MODIFIER | HG02015.hp2 HG02165.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0006a0002c0002t0013 | a0001c0001t0006g0079 a0002c0002t0013g0297 |
2 | 364 | 0.0055 | -530 | c.463 others(17): Show |
PCGF3 | ENSG00000185619.19 | transcript | ENST00000362003.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
PTPRD_chr9_8309246_10618002 | 10404561 | GCCATGTT others(523): Show |
G | intron_variant | MODIFIER | HG00642.hp1 HG00642.hp2 HG01099.hp1 others(26): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(24): Show | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0002g0013 others(26): Show |
29 | 34 | 0.8529 | -530 | c.-59 others(21): Show |
PTPRD | ENSG00000153707.19 | transcript | ENST00000381196.9 | protein_coding | 2/45 | chr9 | TogoVar | |||||||
SEC14L1_chr17_77135969_77222101 | 77215801 | CGTAGGTA others(523): Show |
C | 3_prime_UTR_variant | MODIFIER | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(34): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0006a0001c0002t0006 | a0001c0001t0003g0001 a0001c0001t0006g0001 a0001c0001t0006g0010 others(31): Show |
37 | 427 | 0.0867 | -530 | c.*17 others(11): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1789 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
SLAIN2_chr4_48336529_48431201 | 48363437 | GGGGGGCT others(523): Show |
G | intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0001 | a0001c0001t0027 | a0001c0001t0027g0179 | 1 | 346 | 0.0029 | -530 | c.390 others(17): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
SLC2A13_chr12_39750025_40111081 | 40076412 | CTGATTTT others(523): Show |
C | intron_variant | MODIFIER | HG03704.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0169 | 1 | 212 | 0.0047 | -530 | c.556 others(19): Show |
SLC2A13 | ENSG00000151229.13 | transcript | ENST00000280871.9 | protein_coding | 1/9 | chr12 | TogoVar | |||||||
SORCS2_chr4_7187538_7747827 | 7229813 | GCAGTGTC others(523): Show |
G | intron_variant | MODIFIER | HG00099.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0006others(2): Show | a0001c0001t0005a0001c0002t0007a0001c0006t0002others(3): Show | a0001c0001t0005g0085 a0001c0002t0007g0158 a0001c0002t0007g0159 others(4): Show |
7 | 168 | 0.0417 | -530 | c.480 others(19): Show |
SORCS2 | ENSG00000184985.17 | transcript | ENST00000507866.6 | protein_coding | 1/26 | chr4 | TogoVar | |||||||
TPPP_chr5_654862_698352 | 667855 | CCGTCAGG others(523): Show |
C | intron_variant | MODIFIER | HG00280.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0154 | 1 | 408 | 0.0025 | -530 | c.312 others(17): Show |
TPPP | ENSG00000171368.12 | transcript | ENST00000360578.7 | protein_coding | 2/3 | chr5 | TogoVar | |||||||
TUBGCP2_chr10_133273635_133313872 | 133291945 | CCCTCCGT others(523): Show |
C | intron_variant | MODIFIER | HG01099.hp1 HG02622.hp2 NA19067.hp2 |
a0001 | a0001c0001a0001c0022 | a0001c0001t0001a0001c0001t0004a0001c0022t0001 | a0001c0001t0001g0110 a0001c0001t0004g0227 a0001c0022t0001g0130 |
3 | 281 | 0.0107 | -530 | c.121 others(16): Show |
TUBGCP2 | ENSG00000130640.15 | transcript | ENST00000252936.8 | protein_coding | 8/17 | chr10 | TogoVar |