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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP24_chr4_85470150_86007666 | 85894960 | CAAAAAAA others(36): Show |
C | intron_variant | MODIFIER | HG00423.hp2 HG00639.hp1 HG01433.hp1 others(15): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0021a0001c0002t0002others(8): Show | a0001c0001t0001g0032 a0001c0001t0021g0054 a0001c0002t0002g0004 others(15): Show |
18 | 64 | 0.2813 | -43 | c.269 others(62): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP27_chr17_45388908_45437870 | 45433560 | GAGGAACT others(36): Show |
G | upstream_gene_variant | MODIFIER | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(25): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0004 | a0001c0001t0002a0001c0001t0009a0002c0002t0001others(3): Show | a0001c0001t0002g0002 a0001c0001t0002g0253 a0001c0001t0009g0177 others(17): Show |
28 | 346 | 0.0809 | -43 | c.-11 others(54): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 691 | chr17 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144676417 | GGTGCTGC others(36): Show |
G | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG01891.hp1 others(66): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0024 others(66): Show |
69 | 244 | 0.2828 | -43 | c.-82 others(60): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11590773 | CTCGAAAA others(36): Show |
C | intron_variant | MODIFIER | HG02451.hp1 HG03516.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | 123 | 0.0163 | -43 | c.588 others(62): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGEF28_chr5_73621196_73946990 | 73671712 | ATATATAT others(36): Show |
A | intron_variant | MODIFIER | HG02486.hp2 HG03139.hp2 |
a0002a0011 | a0002c0003a0011c0014 | a0002c0003t0001a0011c0014t0001 | a0002c0003t0001g0128 a0011c0014t0001g0161 |
2 | 175 | 0.0114 | -43 | c.-11 others(62): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73671714 | ATATATAT others(36): Show |
A | intron_variant | MODIFIER | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(8): Show |
a0001a0002a0003others(5): Show | a0001c0025a0002c0002a0003c0007others(5): Show | a0001c0025t0005a0002c0002t0003a0003c0007t0001others(6): Show | a0001c0025t0005g0130 a0002c0002t0003g0124 a0003c0007t0001g0184 others(8): Show |
11 | 143 | 0.0769 | -43 | c.-11 others(62): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73671716 | ATATATAT others(36): Show |
A | intron_variant | MODIFIER | HG01167.hp2 NA21309.hp1 |
a0002a0041 | a0002c0002a0041c0031 | a0002c0002t0001a0041c0031t0004 | a0002c0002t0001g0132 a0041c0031t0004g0113 |
2 | 173 | 0.0116 | -43 | c.-11 others(62): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73737459 | TTTCTTTT others(36): Show |
T | intron_variant | MODIFIER | HG02486.hp1 HG02486.hp2 NA21309.hp1 |
a0004a0011a0041 | a0004c0004a0011c0014a0041c0031 | a0004c0004t0005a0011c0014t0001a0041c0031t0004 | a0004c0004t0005g0183 a0011c0014t0001g0161 a0041c0031t0004g0113 |
3 | 186 | 0.0161 | -43 | c.34- others(60): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111310094 | GAGGACTG others(36): Show |
G | downstream_gene_variant | MODIFIER | HG00558.hp2 HG00741.hp1 HG01081.hp2 others(30): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(9): Show | a0001c0001t0001g0079 a0001c0001t0005g0036 a0001c0001t0006g0015 others(30): Show |
33 | 272 | 0.1213 | -43 | c.*69 others(54): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 4363 | chr13 | TogoVar | |||||||
ARID1A_chr1_26691015_26787104 | 26737764 | CTGAGGCA others(36): Show |
C | intron_variant | MODIFIER | NA20300.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0084 | 1 | 144 | 0.0069 | -43 | c.192 others(62): Show |
ARID1A | ENSG00000117713.21 | transcript | ENST00000324856.13 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARID4B_chr1_235161902_235333179 | 235298891 | AGGCATTT others(36): Show |
A | intron_variant | MODIFIER | HG00642.hp1 HG00733.hp2 HG01070.hp1 others(37): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0010others(6): Show | a0001c0001t0001a0001c0002t0001a0001c0010t0001others(6): Show | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(37): Show |
40 | 270 | 0.1481 | -43 | c.6+2 others(58): Show |
ARID4B | ENSG00000054267.22 | transcript | ENST00000264183.9 | protein_coding | 2/23 | chr1 | TogoVar | |||||||
ARL4C_chr2_234488041_234502081 | 234491051 | ACAAACGA others(36): Show |
A | downstream_gene_variant | MODIFIER | HG00280.hp2 HG00733.hp2 HG01070.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0001 a0001c0001t0006g0006 |
10 | 466 | 0.0215 | -43 | c.*47 others(54): Show |
ARL4C | ENSG00000188042.8 | transcript | ENST00000339728.6 | protein_coding | 1989 | chr2 | TogoVar | |||||||
ARSK_chr5_95550101_95610102 | 95560069 | AGTTCCAT others(36): Show |
A | intron_variant | MODIFIER | NA19059.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0185 | 1 | 334 | 0.0030 | -43 | c.126 others(60): Show |
ARSK | ENSG00000164291.17 | transcript | ENST00000380009.9 | protein_coding | 1/7 | chr5 | TogoVar | |||||||
ART1_chr11_3640128_3669416 | 3663056 | ATCTCATC others(36): Show |
A | intron_variant | MODIFIER | HG00639.hp2 HG01109.hp2 HG01943.hp2 others(8): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0002c0002t0002a0003c0003t0002 | a0001c0001t0002g0015 a0001c0001t0002g0038 a0001c0001t0002g0039 others(7): Show |
11 | 392 | 0.0281 | -43 | c.887 others(59): Show |
ART1 | ENSG00000129744.3 | transcript | ENST00000250693.2 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ART1_chr11_3640128_3669416 | 3663066 | ATCTCATC others(36): Show |
A | intron_variant | MODIFIER | HG00597.hp2 HG01993.hp1 HG03927.hp2 others(16): Show |
a0002a0003 | a0002c0004a0003c0003 | a0002c0004t0002a0003c0003t0002 | a0002c0004t0002g0009 a0003c0003t0002g0003 a0003c0003t0002g0009 others(8): Show |
19 | 380 | 0.0500 | -43 | c.887 others(59): Show |
ART1 | ENSG00000129744.3 | transcript | ENST00000250693.2 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ASAP1_chr8_130047104_130448674 | 130050074 | TGGAGGGC others(36): Show |
T | downstream_gene_variant | MODIFIER | HG04199.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0069 | 1 | 304 | 0.0033 | -43 | c.*46 others(54): Show |
ASAP1 | ENSG00000153317.15 | transcript | ENST00000518721.6 | protein_coding | 2029 | chr8 | TogoVar | |||||||
ASAP1_chr8_130047104_130448674 | 130050114 | CATGGGGG others(36): Show |
C | downstream_gene_variant | MODIFIER | HG01496.hp2 HG02723.hp1 HG03195.hp2 |
a0001a0004 | a0001c0001a0004c0012 | a0001c0001t0012a0004c0012t0027 | a0001c0001t0012g0296 a0001c0001t0012g0298 a0004c0012t0027g0233 |
3 | 301 | 0.0100 | -43 | c.*45 others(54): Show |
ASAP1 | ENSG00000153317.15 | transcript | ENST00000518721.6 | protein_coding | 1989 | chr8 | TogoVar | |||||||
ASAP2_chr2_9201812_9410678 | 9279170 | GAGGGACC others(36): Show |
G | intron_variant | MODIFIER | HG02155.hp2 | a0002 | a0002c0001 | a0002c0001t0001 | a0002c0001t0001g0081 | 1 | 210 | 0.0048 | -43 | c.127 others(57): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ASCC3_chr6_100503194_100886329 | 100853435 | TTTTTGAG others(36): Show |
T | intron_variant | MODIFIER | HG01071.hp1 HG01123.hp1 HG01168.hp1 others(3): Show |
a0001a0003 | a0001c0002a0003c0005 | a0001c0002t0003a0003c0005t0002 | a0001c0002t0003g0153 a0003c0005t0002g0148 a0003c0005t0002g0149 others(3): Show |
6 | 312 | 0.0192 | -43 | c.242 others(60): Show |
ASCC3 | ENSG00000112249.14 | transcript | ENST00000369162.7 | protein_coding | 3/41 | chr6 | TogoVar | |||||||
ASIC2_chr17_33008087_33298295 | 33263630 | CTCTGGCC others(36): Show |
C | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp1 HG01175.hp1 others(31): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(10): Show | a0001c0001t0003g0037 a0001c0001t0003g0046 a0001c0001t0003g0052 others(31): Show |
34 | 238 | 0.1429 | -43 | c.708 others(62): Show |
ASIC2 | ENSG00000108684.15 | transcript | ENST00000225823.7 | protein_coding | 1/9 | chr17 | TogoVar | |||||||
ATAD3B_chr1_1466765_1502848 | 1472036 | ACCCCACC others(36): Show |
A | frameshift_variant | HIGH | NA18959.hp2 | a0023 | a0023c0036 | a0023c0036t0001 | a0023c0036t0001g0003 | 1 | 274 | 0.0036 | -43 | c.153 others(50): Show |
p.Asp others(4): Show |
ATAD3B | ENSG00000160072.20 | transcript | ENST00000673477.1 | protein_coding | 1/16 | 273/4098 | 153/1947 | 51/648 | chr1 | TogoVar | |||
ATAD3B_chr1_1466765_1502848 | 1480176 | AGGGCACA others(36): Show |
A | intron_variant | MODIFIER | HG02109.hp1 HG02602.hp2 HG02717.hp1 others(3): Show |
a0002a0006 | a0002c0002a0006c0009 | a0002c0002t0011a0006c0009t0001 | a0002c0002t0011g0021 a0006c0009t0001g0011 a0006c0009t0001g0111 |
6 | 274 | 0.0219 | -43 | c.445 others(58): Show |
ATAD3B | ENSG00000160072.20 | transcript | ENST00000673477.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ATCAY_chr19_3875685_3933082 | 3908624 | GTCCTCCT others(36): Show |
G | intron_variant | MODIFIER | HG01884.hp1 HG02280.hp2 HG02451.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0043others(1): Show | a0001c0001t0001g0023 a0001c0001t0001g0159 a0001c0001t0001g0183 others(8): Show |
11 | 373 | 0.0295 | -43 | c.647 others(58): Show |
ATCAY | ENSG00000167654.18 | transcript | ENST00000450849.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ATCAY_chr19_3875685_3933082 | 3908632 | CCTCCTCC others(36): Show |
C | intron_variant | MODIFIER | HG03017.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0196 | 1 | 380 | 0.0026 | -43 | c.647 others(58): Show |
ATCAY | ENSG00000167654.18 | transcript | ENST00000450849.7 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ATP11A_chr13_112685038_112892168 | 112767148 | TGTAGGGG others(36): Show |
T | intron_variant | MODIFIER | HG00733.hp1 | a0001 | a0001c0001 | a0001c0001t0062 | a0001c0001t0062g0138 | 1 | 252 | 0.0040 | -43 | c.40- others(60): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ATP11A_chr13_112685038_112892168 | 112803694 | CTCCCCTC others(36): Show |
C | intron_variant | MODIFIER | HG01243.hp2 HG01261.hp1 HG02280.hp2 others(5): Show |
a0001a0008 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0002t0004a0001c0002t0014others(4): Show | a0001c0001t0001g0068 a0001c0001t0001g0210 a0001c0002t0004g0041 others(5): Show |
8 | 252 | 0.0317 | -43 | c.163 others(60): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ATP11A_chr13_112685038_112892168 | 112804200 | CCCCTCCT others(36): Show |
C | intron_variant | MODIFIER | HG00438.hp1 HG01169.hp1 HG01255.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0010a0001c0001t0019a0001c0002t0007others(3): Show | a0001c0001t0010g0004 a0001c0001t0019g0142 a0001c0002t0007g0237 others(4): Show |
7 | 243 | 0.0288 | -43 | c.163 others(58): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ATP12A_chr13_24675408_24717472 | 24682155 | GTGTGGTG others(36): Show |
G | intron_variant | MODIFIER | HG03471.hp1 | a0012 | a0012c0030 | a0012c0030t0001 | a0012c0030t0001g0250 | 1 | 380 | 0.0026 | -43 | c.168 others(58): Show |
ATP12A | ENSG00000075673.12 | transcript | ENST00000381946.5 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ATP6V1H_chr8_53710543_53848245 | 53755702 | ATATATAT others(36): Show |
A | intron_variant | MODIFIER | HG01074.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0075 | 1 | 283 | 0.0035 | -43 | c.127 others(60): Show |
ATP6V1H | ENSG00000047249.18 | transcript | ENST00000359530.7 | protein_coding | 12/13 | chr8 | TogoVar | |||||||
ATP8A2_chr13_25366974_26030851 | 25531398 | TTATATAT others(36): Show |
T | intron_variant | MODIFIER | HG01261.hp2 HG02257.hp2 HG02896.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0008 | a0001c0001t0009a0001c0001t0017a0001c0001t0026others(5): Show | a0001c0001t0009g0065 a0001c0001t0017g0051 a0001c0001t0026g0089 others(5): Show |
8 | 118 | 0.0678 | -43 | c.420 others(58): Show |
ATP8A2 | ENSG00000132932.19 | transcript | ENST00000381655.7 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
ATR_chr3_142444235_142583733 | 142496278 | CTATATAT others(36): Show |
C | intron_variant | MODIFIER | NA19043.hp1 | a0012 | a0012c0021 | a0012c0021t0001 | a0012c0021t0001g0318 | 1 | 22 | 0.0455 | -43 | c.589 others(58): Show |
ATR | ENSG00000175054.16 | transcript | ENST00000350721.9 | protein_coding | 34/46 | chr3 | TogoVar | |||||||
AUTS2_chr7_69593475_70798506 | 70043562 | TTCCTTCC others(36): Show |
T | intron_variant | MODIFIER | HG01243.hp2 | a0001 | a0001c0007 | a0001c0007t0006 | a0001c0007t0006g0027 | 1 | 76 | 0.0132 | -43 | c.523 others(62): Show |
AUTS2 | ENSG00000158321.19 | transcript | ENST00000342771.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
AVPI1_chr10_97672424_97692241 | 97678957 | GTGTGTGT others(36): Show |
G | intron_variant | MODIFIER | HG02897.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0069 | 1 | 352 | 0.0028 | -43 | c.287 others(58): Show |
AVPI1 | ENSG00000119986.7 | transcript | ENST00000370626.4 | protein_coding | 2/2 | chr10 | TogoVar | |||||||
B3GNTL1_chr17_82937149_83056770 | 83003037 | CTCCGCGT others(36): Show |
C | intron_variant | MODIFIER | HG02572.hp2 HG04199.hp2 |
a0001 | a0001c0003a0001c0014 | a0001c0003t0009a0001c0014t0002 | a0001c0003t0009g0213 a0001c0014t0002g0012 |
2 | 257 | 0.0078 | -43 | c.459 others(60): Show |
B3GNTL1 | ENSG00000175711.9 | transcript | ENST00000320865.4 | protein_coding | 6/12 | chr17 | TogoVar | |||||||
B3GNTL1_chr17_82937149_83056770 | 83003266 | CTCCGCGT others(36): Show |
C | intron_variant | MODIFIER | HG00280.hp2 HG00735.hp2 HG01081.hp1 others(26): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0004a0001c0002t0001a0001c0002t0002others(13): Show | a0001c0001t0004g0229 a0001c0002t0001g0117 a0001c0002t0001g0130 others(25): Show |
29 | 247 | 0.1174 | -43 | c.459 others(60): Show |
B3GNTL1 | ENSG00000175711.9 | transcript | ENST00000320865.4 | protein_coding | 6/12 | chr17 | TogoVar | |||||||
B3GNTL1_chr17_82937149_83056770 | 83003345 | CTCCGCGT others(36): Show |
C | intron_variant | MODIFIER | NA19080.hp2 | a0001 | a0001c0002 | a0001c0002t0008 | a0001c0002t0008g0106 | 1 | 262 | 0.0038 | -43 | c.459 others(60): Show |
B3GNTL1 | ENSG00000175711.9 | transcript | ENST00000320865.4 | protein_coding | 6/12 | chr17 | TogoVar | |||||||
B3GNTL1_chr17_82937149_83056770 | 83003384 | TGCAGTCC others(36): Show |
T | intron_variant | MODIFIER | HG02080.hp2 NA18953.hp1 NA18959.hp2 others(2): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0005 | a0001c0001t0002a0001c0001t0019a0001c0001t0027others(2): Show | a0001c0001t0002g0179 a0001c0001t0019g0182 a0001c0001t0027g0181 others(2): Show |
5 | 265 | 0.0189 | -43 | c.459 others(60): Show |
B3GNTL1 | ENSG00000175711.9 | transcript | ENST00000320865.4 | protein_coding | 6/12 | chr17 | TogoVar | |||||||
B3GNTL1_chr17_82937149_83056770 | 83003467 | CTCCGCGT others(36): Show |
C | intron_variant | MODIFIER | HG00408.hp2 | a0001 | a0001c0006 | a0001c0006t0002 | a0001c0006t0002g0041 | 1 | 255 | 0.0039 | -43 | c.459 others(60): Show |
B3GNTL1 | ENSG00000175711.9 | transcript | ENST00000320865.4 | protein_coding | 6/12 | chr17 | TogoVar | |||||||
B3GNTL1_chr17_82937149_83056770 | 83003578 | GCCCTCCC others(36): Show |
G | intron_variant | MODIFIER | HG00280.hp2 HG00735.hp2 HG01069.hp1 others(29): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0004a0001c0001t0011a0001c0002t0001others(15): Show | a0001c0001t0004g0229 a0001c0001t0004g0230 a0001c0001t0011g0068 others(27): Show |
32 | 265 | 0.1208 | -43 | c.459 others(60): Show |
B3GNTL1 | ENSG00000175711.9 | transcript | ENST00000320865.4 | protein_coding | 6/12 | chr17 | TogoVar | |||||||
B3GNTL1_chr17_82937149_83056770 | 83003822 | ACCCTCCC others(36): Show |
A | intron_variant | MODIFIER | HG00280.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0158 | 1 | 143 | 0.0070 | -43 | c.459 others(60): Show |
B3GNTL1 | ENSG00000175711.9 | transcript | ENST00000320865.4 | protein_coding | 6/12 | chr17 | TogoVar | |||||||
B3GNTL1_chr17_82937149_83056770 | 83003919 | CTCCGCGT others(36): Show |
C | intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0006 | a0001c0006t0033 | a0001c0006t0033g0046 | 1 | 257 | 0.0039 | -43 | c.459 others(60): Show |
B3GNTL1 | ENSG00000175711.9 | transcript | ENST00000320865.4 | protein_coding | 6/12 | chr17 | TogoVar | |||||||
B3GNTL1_chr17_82937149_83056770 | 83004192 | CTCCGCGT others(36): Show |
C | intron_variant | MODIFIER | HG02630.hp1 | a0001 | a0001c0006 | a0001c0006t0018 | a0001c0006t0018g0017 | 1 | 181 | 0.0055 | -43 | c.459 others(58): Show |
B3GNTL1 | ENSG00000175711.9 | transcript | ENST00000320865.4 | protein_coding | 6/12 | chr17 | TogoVar | |||||||
B3GNTL1_chr17_82937149_83056770 | 83004508 | CTCCGCGT others(36): Show |
C | intron_variant | MODIFIER | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(106): Show |
a0001a0002a0006 | a0001c0001a0001c0002a0001c0003others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(45): Show | a0001c0001t0001g0004 a0001c0001t0001g0166 a0001c0001t0001g0167 others(101): Show |
109 | 260 | 0.4192 | -43 | c.459 others(58): Show |
B3GNTL1 | ENSG00000175711.9 | transcript | ENST00000320865.4 | protein_coding | 6/12 | chr17 | TogoVar | |||||||
B3GNTL1_chr17_82937149_83056770 | 83004719 | TGCAGTCC others(36): Show |
T | intron_variant | MODIFIER | HG00408.hp2 HG02486.hp1 HG02572.hp2 others(4): Show |
a0001 | a0001c0001a0001c0006a0001c0007others(1): Show | a0001c0001t0002a0001c0001t0011a0001c0001t0039others(4): Show | a0001c0001t0002g0134 a0001c0001t0011g0068 a0001c0001t0039g0259 others(4): Show |
7 | 265 | 0.0264 | -43 | c.459 others(58): Show |
B3GNTL1 | ENSG00000175711.9 | transcript | ENST00000320865.4 | protein_coding | 6/12 | chr17 | TogoVar | |||||||
B4GALT4_chr3_119206742_119245878 | 119242764 | AGCCAGCC others(36): Show |
A | upstream_gene_variant | MODIFIER | HG00639.hp1 HG01123.hp2 HG01952.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0018 a0001c0001t0003g0041 a0001c0001t0003g0143 others(2): Show |
8 | 434 | 0.0184 | -43 | c.-23 others(54): Show |
B4GALT4 | ENSG00000121578.13 | transcript | ENST00000393765.7 | protein_coding | 1887 | chr3 | TogoVar | |||||||
BACE2_chr21_41163160_41287530 | 41249148 | TTAGTGAG others(36): Show |
T | intron_variant | MODIFIER | HG00408.hp1 HG01074.hp2 HG01109.hp1 others(21): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0015a0001c0001t0019others(2): Show | a0001c0001t0004g0018 a0001c0001t0004g0019 a0001c0001t0004g0026 others(21): Show |
24 | 270 | 0.0889 | -43 | c.985 others(60): Show |
BACE2 | ENSG00000182240.16 | transcript | ENST00000330333.11 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr21 | TogoVar | ||||||
BATF2_chr11_64982945_65001971 | 64983517 | TTATTTTA others(36): Show |
T | downstream_gene_variant | MODIFIER | HG01069.hp2 HG01071.hp1 HG04228.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0012 | 3 | 401 | 0.0075 | -43 | c.*55 others(54): Show |
BATF2 | ENSG00000168062.10 | transcript | ENST00000301887.9 | protein_coding | 4427 | chr11 | TogoVar | |||||||
BAZ2B_chr2_159313979_159621548 | 159325074 | ATATTATA others(36): Show |
A | intron_variant | MODIFIER | HG00558.hp2 NA18984.hp1 |
a0004a0008 | a0004c0004a0008c0011 | a0004c0004t0001a0008c0011t0001 | a0004c0004t0001g0119 a0008c0011t0001g0084 |
2 | 214 | 0.0093 | -43 | c.621 others(60): Show |
BAZ2B | ENSG00000123636.19 | transcript | ENST00000392783.7 | protein_coding | 35/36 | chr2 | TogoVar | |||||||
BCL11A_chr2_60452194_60558654 | 60507340 | AAGGGAAG others(36): Show |
A | intron_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0075 | 1 | 232 | 0.0043 | -43 | c.386 others(62): Show |
BCL11A | ENSG00000119866.22 | transcript | ENST00000642384.2 | protein_coding | 2/3 | chr2 | TogoVar | |||||||
BCL9_chr1_147536501_147631216 | 147541076 | AGAGAGAG others(36): Show |
A | upstream_gene_variant | MODIFIER | HG00597.hp1 HG01169.hp1 HG02602.hp1 others(18): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(5): Show | a0001c0001t0001g0006 a0001c0001t0001g0064 a0001c0001t0001g0102 others(16): Show |
21 | 314 | 0.0669 | -43 | c.-10 others(54): Show |
BCL9 | ENSG00000116128.12 | transcript | ENST00000234739.8 | protein_coding | 424 | chr1 | TogoVar |