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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
APOBEC1_chr12_7644400_7670908 | 7660375 | G | GGAAGGAA others(45): Show |
intron_variant | MODIFIER | HG00280.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0349 | 1 | 432 | 0.0023 | 52 | c.16+ others(67): Show |
APOBEC1 | ENSG00000111701.7 | transcript | ENST00000229304.5 | protein_coding | 1/4 | chr12 | TogoVar | |||||||
APOBEC1_chr12_7644400_7670908 | 7660375 | G | GGAAGGAA others(45): Show |
intron_variant | MODIFIER | HG04184.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0356 | 1 | 432 | 0.0023 | 52 | c.16+ others(67): Show |
APOBEC1 | ENSG00000111701.7 | transcript | ENST00000229304.5 | protein_coding | 1/4 | chr12 | TogoVar | |||||||
APOBEC3F_chr22_39035864_39060972 | 39052885 | C | CCTCTCCC others(45): Show |
3_prime_UTR_variant | MODIFIER | HG02698.hp1 | a0002 | a0002c0002 | a0002c0002t0044 | a0002c0002t0044g0163 | 1 | 422 | 0.0024 | 52 | c.*19 others(61): Show |
APOBEC3F | ENSG00000128394.17 | transcript | ENST00000308521.10 | protein_coding | 7/7 | 195 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARC_chr8_142606049_142619479 | 142610013 | T | TCAGGGGA others(45): Show |
downstream_gene_variant | MODIFIER | HG02572.hp2 HG02735.hp2 NA18981.hp1 |
a0001a0002 | a0001c0001a0001c0002a0002c0018 | a0001c0001t0002a0001c0002t0003a0002c0018t0003 | a0001c0001t0002g0002 a0001c0002t0003g0003 a0002c0018t0003g0029 |
3 | 420 | 0.0071 | 52 | c.*25 others(63): Show |
ARC | ENSG00000198576.4 | transcript | ENST00000356613.4 | protein_coding | 1035 | chr8 | TogoVar | |||||||
ARC_chr8_142606049_142619479 | 142610013 | T | TCAGGGGA others(45): Show |
downstream_gene_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(123): Show |
a0001a0002a0004others(2): Show | a0001c0002a0002c0017a0004c0010others(2): Show | a0001c0002t0003a0001c0002t0004a0001c0002t0005others(11): Show | a0001c0002t0003g0003 a0001c0002t0004g0049 a0001c0002t0005g0005 others(12): Show |
126 | 420 | 0.3000 | 52 | c.*25 others(63): Show |
ARC | ENSG00000198576.4 | transcript | ENST00000356613.4 | protein_coding | 1035 | chr8 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24656938 | T | TGGGGGGG others(45): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(46): Show |
a0001a0003a0007others(3): Show | a0001c0001a0003c0003a0007c0008others(3): Show | a0001c0001t0001a0001c0001t0013a0003c0003t0001others(5): Show | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0160 others(46): Show |
49 | 352 | 0.1392 | 52 | c.268 others(71): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38472429 | C | CGGGGGCT others(45): Show |
intron_variant | MODIFIER | HG02486.hp1 HG03195.hp1 |
a0001a0004 | a0001c0007a0004c0064 | a0001c0007t0003a0004c0064t0004 | a0001c0007t0003g0051 a0004c0064t0004g0302 |
2 | 309 | 0.0065 | 52 | c.211 others(69): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38513074 | T | TTAAATAT others(45): Show |
downstream_gene_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0077 | 1 | 309 | 0.0032 | 52 | c.*21 others(63): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 690 | chr17 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144531183 | C | CAGGGCAG others(45): Show |
intron_variant | MODIFIER | HG01975.hp2 HG02922.hp1 HG03139.hp2 others(2): Show |
a0001a0007 | a0001c0001a0007c0013 | a0001c0001t0002a0007c0013t0002 | a0001c0001t0002g0123 a0001c0001t0002g0131 a0001c0001t0002g0134 others(2): Show |
5 | 246 | 0.0203 | 52 | c.298 others(69): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144531191 | A | AGAGCAGC others(45): Show |
intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0019 | a0001c0019t0001 | a0001c0019t0001g0064 | 1 | 246 | 0.0041 | 52 | c.298 others(69): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144531191 | A | AGAGCAGC others(45): Show |
intron_variant | MODIFIER | HG03491.hp2 HG03688.hp2 NA19091.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0191 |
3 | 246 | 0.0122 | 52 | c.298 others(69): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144531242 | C | CAGGGCAG others(45): Show |
intron_variant | MODIFIER | HG01071.hp1 HG01358.hp1 HG02293.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0027 a0001c0001t0001g0196 a0001c0001t0001g0213 |
3 | 246 | 0.0122 | 52 | c.298 others(69): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144531242 | C | CAGGGCAG others(45): Show |
intron_variant | MODIFIER | HG02300.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0115 | 1 | 246 | 0.0041 | 52 | c.298 others(69): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144531244 | G | GGGCAGGG others(45): Show |
intron_variant | MODIFIER | HG01346.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0124 | 1 | 246 | 0.0041 | 52 | c.298 others(69): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144531253 | G | GCAGCAGG others(45): Show |
intron_variant | MODIFIER | HG00639.hp1 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0011 | 1 | 246 | 0.0041 | 52 | c.298 others(69): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144531301 | C | CAGGGCAG others(45): Show |
intron_variant | MODIFIER | HG03139.hp2 NA20300.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0131 a0001c0001t0002g0134 |
2 | 246 | 0.0081 | 52 | c.298 others(69): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100779542 | A | ATATATAT others(45): Show |
intron_variant | MODIFIER | HG00323.hp2 HG00735.hp2 HG01106.hp2 others(2): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0007 | a0001c0001t0001a0002c0002t0012a0003c0007t0005 | a0001c0001t0001g0007 a0001c0001t0001g0072 a0002c0002t0012g0024 others(2): Show |
5 | 286 | 0.0175 | 52 | c.250 others(69): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1089375 | G | GCTGCCGG others(45): Show |
downstream_gene_variant | MODIFIER | NA19086.hp2 | a0005 | a0005c0015 | a0005c0015t0001 | a0005c0015t0001g0276 | 1 | 418 | 0.0024 | 52 | c.*33 others(63): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 2748 | chr19 | TogoVar | |||||||
ARHGDIG_chr16_275591_288010 | 285931 | C | CCCCAACC others(45): Show |
downstream_gene_variant | MODIFIER | HG01069.hp1 HG01071.hp1 HG03486.hp1 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0015 | a0001c0001t0006g0016 a0001c0001t0015g0020 |
3 | 442 | 0.0068 | 52 | c.*31 others(63): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2922 | chr16 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1954952 | C | CAGGTGCT others(45): Show |
intron_variant | MODIFIER | HG00621.hp1 NA18971.hp2 |
a0001a0002 | a0001c0004a0002c0078 | a0001c0004t0002a0002c0078t0002 | a0001c0004t0002g0252 a0002c0078t0002g0036 |
2 | 363 | 0.0055 | 52 | c.352 others(71): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1954960 | C | CCCTGAAA others(45): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02895.hp2 HG03486.hp1 |
a0001a0011 | a0001c0003a0001c0108a0011c0029 | a0001c0003t0051a0001c0108t0042a0011c0029t0007 | a0001c0003t0051g0118 a0001c0108t0042g0330 a0011c0029t0007g0202 |
3 | 363 | 0.0083 | 52 | c.352 others(71): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1955050 | G | GTAGCCAG others(45): Show |
intron_variant | MODIFIER | HG04184.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0341 | 1 | 363 | 0.0028 | 52 | c.352 others(71): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1955106 | C | CAGGTGCT others(45): Show |
intron_variant | MODIFIER | HG02056.hp1 NA18948.hp1 NA18951.hp2 others(6): Show |
a0001a0002a0007 | a0001c0001a0001c0004a0001c0112others(5): Show | a0001c0001t0002a0001c0004t0002a0001c0112t0046others(5): Show | a0001c0001t0002g0271 a0001c0004t0002g0240 a0001c0004t0002g0340 others(6): Show |
9 | 363 | 0.0248 | 52 | c.352 others(71): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1955106 | C | CAGGTGCT others(45): Show |
intron_variant | MODIFIER | HG01358.hp2 HG01934.hp2 HG01943.hp1 others(28): Show |
a0001a0002a0003others(2): Show | a0001c0002a0001c0003a0001c0005others(14): Show | a0001c0002t0001a0001c0003t0001a0001c0003t0007others(19): Show | a0001c0002t0001g0270 a0001c0003t0001g0026 a0001c0003t0001g0033 others(28): Show |
31 | 363 | 0.0854 | 52 | c.352 others(71): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1955114 | C | CCCTGAAA others(45): Show |
intron_variant | MODIFIER | HG02258.hp1 HG03491.hp2 |
a0006a0019 | a0006c0090a0019c0096 | a0006c0090t0003a0019c0096t0016 | a0006c0090t0003g0024 a0019c0096t0016g0103 |
2 | 363 | 0.0055 | 52 | c.352 others(71): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1955157 | C | CAGGTGCA others(45): Show |
intron_variant | MODIFIER | HG03209.hp1 NA19066.hp1 |
a0001a0021 | a0001c0066a0021c0091 | a0001c0066t0022a0021c0091t0034 | a0001c0066t0022g0227 a0021c0091t0034g0350 |
2 | 363 | 0.0055 | 52 | c.352 others(71): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1955343 | G | GTGTTTCT others(45): Show |
intron_variant | MODIFIER | HG03098.hp2 NA20300.hp1 |
a0001 | a0001c0046 | a0001c0046t0009 | a0001c0046t0009g0331 a0001c0046t0009g0334 |
2 | 363 | 0.0055 | 52 | c.352 others(71): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1955387 | T | TACTCTCA others(45): Show |
intron_variant | MODIFIER | HG01981.hp2 | a0001 | a0001c0069 | a0001c0069t0001 | a0001c0069t0001g0012 | 1 | 363 | 0.0028 | 52 | c.352 others(71): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1955439 | C | CACTCACT others(45): Show |
intron_variant | MODIFIER | HG02922.hp1 | a0001 | a0001c0094 | a0001c0094t0009 | a0001c0094t0009g0186 | 1 | 363 | 0.0028 | 52 | c.352 others(71): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF18_chr19_7343937_7477478 | 7367844 | A | ATATATAT others(45): Show |
intron_variant | MODIFIER | HG02622.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
a0002 | a0002c0004 | a0002c0004t0004 | a0002c0004t0004g0018 a0002c0004t0004g0019 a0002c0004t0004g0064 others(2): Show |
5 | 298 | 0.0168 | 52 | c.15+ others(67): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136727355 | T | TTCTTTCT others(45): Show |
intron_variant | MODIFIER | HG01109.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0011 | 1 | 247 | 0.0041 | 52 | c.732 others(69): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | TogoVar | |||||||
ARID1B_chr6_156772378_157215779 | 156893045 | C | CTTTTTTT others(45): Show |
intron_variant | MODIFIER | HG01496.hp2 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0064 | 1 | 150 | 0.0067 | 52 | c.198 others(71): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 157039670 | C | CTTCCTTC others(45): Show |
intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0057 | 1 | 150 | 0.0067 | 52 | c.224 others(73): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 157039674 | C | CTTCCTTC others(45): Show |
intron_variant | MODIFIER | HG02257.hp1 HG02895.hp1 HG06807.hp1 others(1): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0035 | a0001c0001t0001a0001c0002t0001a0003c0035t0022 | a0001c0001t0001g0070 a0001c0001t0001g0078 a0001c0002t0001g0077 others(1): Show |
4 | 150 | 0.0267 | 52 | c.224 others(73): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARID1B_chr6_156772378_157215779 | 157039674 | C | CTTCCTTC others(45): Show |
intron_variant | MODIFIER | NA20300.hp1 | a0002 | a0002c0003 | a0002c0003t0009 | a0002c0003t0009g0053 | 1 | 150 | 0.0067 | 52 | c.224 others(73): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
ARL16_chr17_81676187_81688797 | 81686754 | G | GCTGCTGT others(45): Show |
upstream_gene_variant | MODIFIER | HG00099.hp2 HG00408.hp2 HG00544.hp1 others(65): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0006 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0013 others(2): Show |
68 | 444 | 0.1532 | 52 | c.-30 others(63): Show |
ARL16 | ENSG00000214087.9 | transcript | ENST00000622299.5 | protein_coding | 2958 | chr17 | TogoVar | |||||||
ARL16_chr17_81676187_81688797 | 81686866 | C | CCCACCGG others(45): Show |
upstream_gene_variant | MODIFIER | NA18967.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0002 | 1 | 444 | 0.0023 | 52 | c.-31 others(63): Show |
ARL16 | ENSG00000214087.9 | transcript | ENST00000622299.5 | protein_coding | 3070 | chr17 | TogoVar | |||||||
ARL6IP5_chr3_69079937_69111092 | 69110853 | A | AAAAAAAA others(45): Show |
downstream_gene_variant | MODIFIER | HG01884.hp2 NA18993.hp2 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0028 a0001c0002t0002g0264 |
2 | 434 | 0.0046 | 52 | c.*62 others(63): Show |
ARL6IP5 | ENSG00000144746.7 | transcript | ENST00000273258.4 | protein_coding | 4762 | chr3 | TogoVar | |||||||
ARL6IP5_chr3_69079937_69111092 | 69110853 | A | AAAAAAAA others(45): Show |
downstream_gene_variant | MODIFIER | NA18991.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0270 | 1 | 434 | 0.0023 | 52 | c.*62 others(63): Show |
ARL6IP5 | ENSG00000144746.7 | transcript | ENST00000273258.4 | protein_coding | 4762 | chr3 | TogoVar | |||||||
ARMC10_chr7_103070140_103104759 | 103099575 | C | CGTGTGTG others(45): Show |
3_prime_UTR_variant | MODIFIER | HG01496.hp2 HG02109.hp2 NA18963.hp1 |
a0001 | a0001c0001 | a0001c0001t0062a0001c0001t0063a0001c0001t0077 | a0001c0001t0062g0041 a0001c0001t0063g0106 a0001c0001t0077g0141 |
3 | 390 | 0.0077 | 52 | c.*10 others(63): Show |
ARMC10 | ENSG00000170632.14 | transcript | ENST00000323716.8 | protein_coding | 7/7 | 1041 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ASAP1_chr8_130047104_130448674 | 130072824 | T | TGTGTGTG others(45): Show |
intron_variant | MODIFIER | HG02071.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0210 | 1 | 308 | 0.0033 | 52 | c.270 others(71): Show |
ASAP1 | ENSG00000153317.15 | transcript | ENST00000518721.6 | protein_coding | 27/29 | chr8 | TogoVar | |||||||
ASAP1_chr8_130047104_130448674 | 130072824 | T | TGTGTGTG others(45): Show |
intron_variant | MODIFIER | HG03654.hp1 | a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0049 | 1 | 308 | 0.0033 | 52 | c.270 others(71): Show |
ASAP1 | ENSG00000153317.15 | transcript | ENST00000518721.6 | protein_coding | 27/29 | chr8 | TogoVar | |||||||
ASAP1_chr8_130047104_130448674 | 130072824 | T | TGTGTGTG others(45): Show |
intron_variant | MODIFIER | HG03831.hp2 NA18947.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | 308 | 0.0065 | 52 | c.270 others(71): Show |
ASAP1 | ENSG00000153317.15 | transcript | ENST00000518721.6 | protein_coding | 27/29 | chr8 | TogoVar | |||||||
ASAP1_chr8_130047104_130448674 | 130072825 | G | GTGTGTGT others(45): Show |
intron_variant | MODIFIER | HG02717.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0033 | 1 | 308 | 0.0033 | 52 | c.270 others(71): Show |
ASAP1 | ENSG00000153317.15 | transcript | ENST00000518721.6 | protein_coding | 27/29 | chr8 | TogoVar | |||||||
ASAP2_chr2_9201812_9410678 | 9406007 | C | CAGTCTTC others(45): Show |
downstream_gene_variant | MODIFIER | HG00642.hp2 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0059 | 1 | 210 | 0.0048 | 52 | c.*26 others(63): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 330 | chr2 | TogoVar | |||||||
ASAP2_chr2_9201812_9410678 | 9406008 | A | AGTCTTCC others(45): Show |
downstream_gene_variant | MODIFIER | HG03831.hp1 | a0002 | a0002c0001 | a0002c0001t0001 | a0002c0001t0001g0100 | 1 | 210 | 0.0048 | 52 | c.*26 others(63): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 331 | chr2 | TogoVar | |||||||
ASAP2_chr2_9201812_9410678 | 9406191 | G | GTGTGTGT others(45): Show |
downstream_gene_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0046 | 1 | 210 | 0.0048 | 52 | c.*28 others(63): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 514 | chr2 | TogoVar | |||||||
ASAP2_chr2_9201812_9410678 | 9406199 | T | TTGTCACT others(45): Show |
downstream_gene_variant | MODIFIER | HG01257.hp1 | a0002 | a0002c0001 | a0002c0001t0001 | a0002c0001t0001g0086 | 1 | 210 | 0.0048 | 52 | c.*28 others(63): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 522 | chr2 | TogoVar | |||||||
ASAP2_chr2_9201812_9410678 | 9406228 | C | CGTCTTCC others(45): Show |
downstream_gene_variant | MODIFIER | HG01106.hp1 HG02257.hp2 |
a0001a0002 | a0001c0003a0002c0005 | a0001c0003t0004a0002c0005t0001 | a0001c0003t0004g0011 a0002c0005t0001g0132 |
2 | 210 | 0.0095 | 52 | c.*29 others(63): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 551 | chr2 | TogoVar | |||||||
ASAP2_chr2_9201812_9410678 | 9406367 | T | TTGTCACT others(45): Show |
downstream_gene_variant | MODIFIER | HG01261.hp2 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0026 | 1 | 210 | 0.0048 | 52 | c.*30 others(63): Show |
ASAP2 | ENSG00000151693.11 | transcript | ENST00000281419.8 | protein_coding | 690 | chr2 | TogoVar |