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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
MAN2B1_chr19_12641512_12671742 | 12649477 | C | CTTTTTTT others(6): Show |
intron_variant | MODIFIER | HG02809.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
a0001a0004 | a0001c0001a0004c0005 | a0001c0001t0001a0004c0005t0001 | a0001c0001t0001g0049a0001c0001t0001g0050a0004c0005t0001g0212others(1): Show | 4 | 380 | 0.0105 | 13 | c.226 others(28): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 18/23 | chr19 | TogoVar | ||||||
MAN2B1_chr19_12641512_12671742 | 12661910 | T | TCTCGGCT others(6): Show |
intron_variant | MODIFIER | NA19084.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0052 | 1 | 380 | 0.0026 | 13 | c.910 others(28): Show |
MAN2B1 | ENSG00000104774.13 | transcript | ENST00000456935.7 | protein_coding | 6/23 | chr19 | TogoVar | ||||||
MAN2B2_chr4_6570189_6628362 | 6623526 | T | TGCACCAG others(6): Show |
downstream_gene_variant | MODIFIER | HG03209.hp1 | a0009 | a0009c0028 | a0009c0028t0003 | a0009c0028t0003g0047 | 1 | 362 | 0.0028 | 13 | c.*22 others(24): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 165 | chr4 | TogoVar | ||||||
MANEA_chr6_95572535_95614452 | 95601716 | A | ATTTTTTT others(6): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0003 | a0003c0003 | a0003c0003t0007 | a0003c0003t0007g0200 | 1 | 410 | 0.0024 | 13 | c.655 others(30): Show |
MANEA | ENSG00000172469.17 | transcript | ENST00000358812.9 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
MANSC1_chr12_12321056_12355242 | 12322993 | G | GAGGGGGG others(6): Show |
downstream_gene_variant | MODIFIER | HG01358.hp2 HG02155.hp2 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0017 | a0001c0001t0003g0258a0001c0001t0017g0286 | 2 | 322 | 0.0062 | 13 | c.*70 others(24): Show |
MANSC1 | ENSG00000111261.14 | transcript | ENST00000535902.6 | protein_coding | 3062 | chr12 | TogoVar | ||||||
MAP1A_chr15_43512608_43536611 | 43536069 | G | GATAAGTT others(6): Show |
downstream_gene_variant | MODIFIER | HG03516.hp1 | a0006 | a0006c0006 | a0006c0006t0001 | a0006c0006t0001g0004 | 1 | 340 | 0.0029 | 13 | c.*58 others(24): Show |
MAP1A | ENSG00000166963.13 | transcript | ENST00000300231.6 | protein_coding | 4459 | chr15 | TogoVar | ||||||
MAP1LC3B_chr16_87387336_87409774 | 87391627 | G | GGGGGACT others(6): Show |
upstream_gene_variant | MODIFIER | HG01109.hp1 HG01167.hp2 HG01891.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0016others(1): Show | a0001c0001t0001g0107a0001c0001t0003g0038a0001c0001t0003g0092others(5): Show | 8 | 420 | 0.0191 | 13 | c.-80 others(22): Show |
MAP1LC3B | ENSG00000140941.14 | transcript | ENST00000268607.10 | protein_coding | 708 | chr16 | TogoVar | ||||||
MAP1LC3C_chr1_241990490_242004098 | 241996909 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG01074.hp2 HG01981.hp1 NA18990.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0024a0001c0001t0001g0055a0001c0001t0002g0065 | 5 | 452 | 0.0111 | 13 | c.222 others(28): Show |
MAP1LC3C | ENSG00000197769.6 | transcript | ENST00000357246.4 | protein_coding | 3/3 | chr1 | TogoVar | ||||||
MAP1S_chr19_17714480_17739513 | 17738321 | C | CAAAAAAA others(6): Show |
downstream_gene_variant | MODIFIER | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(11): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0001a0001c0008t0001 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0008t0001g0013 | 14 | 290 | 0.0483 | 13 | c.*38 others(24): Show |
MAP1S | ENSG00000130479.11 | transcript | ENST00000324096.9 | protein_coding | 3809 | chr19 | TogoVar | ||||||
MAP2K1_chr15_66381912_66496544 | 66392255 | G | GTTTTTTT others(6): Show |
intron_variant | MODIFIER | HG02280.hp2 HG02896.hp1 HG02896.hp2 others(8): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0013a0001c0006t0001 | a0001c0001t0001g0010a0001c0001t0001g0327a0001c0001t0001g0328others(8): Show | 11 | 372 | 0.0296 | 13 | c.80+ others(28): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
MAP2K4_chr17_12015877_12148828 | 12041828 | A | AAAGAACT others(6): Show |
intron_variant | MODIFIER | NA19075.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0035 | 1 | 322 | 0.0031 | 13 | c.116 others(32): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
MAP2K4_chr17_12015877_12148828 | 12088458 | T | TTAAATAT others(6): Show |
intron_variant | MODIFIER | HG02040.hp1 NA18906.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0018 | a0001c0001t0001g0207a0001c0001t0018g0047 | 2 | 322 | 0.0062 | 13 | c.393 others(30): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
MAP2K4_chr17_12015877_12148828 | 12096067 | T | TCCCCCCC others(6): Show |
intron_variant | MODIFIER | NA19055.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0129 | 1 | 322 | 0.0031 | 13 | c.513 others(28): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
MAP2K5_chr15_67537703_67812114 | 67547077 | A | ACACACAC others(6): Show |
intron_variant | MODIFIER | NA18967.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0204 | 1 | 278 | 0.0036 | 13 | c.136 others(30): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 1/21 | chr15 | TogoVar | ||||||
MAP2K5_chr15_67537703_67812114 | 67547110 | A | ACACACAC others(6): Show |
intron_variant | MODIFIER | HG02809.hp2 HG03139.hp2 HG03579.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0002 | a0001c0001t0002g0140a0001c0001t0002g0141a0001c0001t0002g0142others(1): Show | 4 | 278 | 0.0144 | 13 | c.136 others(30): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 1/21 | chr15 | TogoVar | ||||||
MAP2K5_chr15_67537703_67812114 | 67634367 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG01070.hp2 HG01081.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | 278 | 0.0072 | 13 | c.585 others(30): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
MAP2K5_chr15_67537703_67812114 | 67769853 | G | GTAATAAG others(6): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0160a0001c0001t0001g0181a0001c0001t0001g0182others(9): Show | 12 | 278 | 0.0432 | 13 | c.119 others(30): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
MAP2_chr2_209419047_209739112 | 209540660 | A | AAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0019 | 1 | 148 | 0.0068 | 13 | c.-17 others(34): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MAP2_chr2_209419047_209739112 | 209593634 | A | AAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG03710.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0114 | 1 | 148 | 0.0068 | 13 | c.-10 others(34): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MAP2_chr2_209419047_209739112 | 209631005 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG01891.hp2 HG03098.hp1 |
a0001a0002 | a0001c0001a0002c0005 | a0001c0001t0025a0002c0005t0011 | a0001c0001t0025g0141a0002c0005t0011g0072 | 2 | 148 | 0.0135 | 13 | c.-30 others(30): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MAP3K10_chr19_40186426_40220575 | 40195471 | C | CTTTTTTT others(6): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0206 | 1 | 398 | 0.0025 | 13 | c.682 others(30): Show |
MAP3K10 | ENSG00000130758.8 | transcript | ENST00000253055.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
MAP3K12_chr12_53474669_53504458 | 53491301 | A | AAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG00639.hp1 HG00639.hp2 HG01099.hp2 others(29): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(3): Show | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0082others(29): Show | 32 | 328 | 0.0976 | 13 | c.-37 others(30): Show |
MAP3K12 | ENSG00000139625.13 | transcript | ENST00000547488.6 | protein_coding | 1/13 | chr12 | TogoVar | ||||||
MAP3K13_chr3_185358136_185494094 | 185395357 | C | CTTTTTTT others(6): Show |
intron_variant | MODIFIER | HG00558.hp1 HG02074.hp1 HG02083.hp1 others(23): Show |
a0001a0009 | a0001c0001a0001c0003a0009c0017 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0002g0017others(23): Show | 26 | 278 | 0.0935 | 13 | c.-86 others(32): Show |
MAP3K13 | ENSG00000073803.14 | transcript | ENST00000265026.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
MAP3K13_chr3_185358136_185494094 | 185454733 | T | TATCATAT others(6): Show |
intron_variant | MODIFIER | HG01081.hp2 HG01981.hp1 HG02071.hp2 others(11): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(3): Show | a0001c0001t0001g0251a0001c0001t0002g0002a0001c0001t0002g0065others(11): Show | 14 | 278 | 0.0504 | 13 | c.127 others(32): Show |
MAP3K13 | ENSG00000073803.14 | transcript | ENST00000265026.8 | protein_coding | 7/13 | chr3 | TogoVar | ||||||
MAP3K13_chr3_185358136_185494094 | 185455716 | G | GATATATA others(6): Show |
intron_variant | MODIFIER | HG00408.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0055 | 1 | 278 | 0.0036 | 13 | c.127 others(32): Show |
MAP3K13 | ENSG00000073803.14 | transcript | ENST00000265026.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
MAP3K15_chrX_19355059_19520508 | 19426818 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG01243.hp1 HG01891.hp2 HG02015.hp1 others(5): Show |
a0000a0001a0002others(1): Show | a0000c0021a0001c0001a0002c0002others(1): Show | a0000c0021t0007a0001c0001t0002a0002c0002t0007others(4): Show | a0000c0021t0007g0054a0001c0001t0002g0085a0002c0002t0007g0130others(5): Show | 8 | 163 | 0.0491 | 13 | c.116 others(30): Show |
MAP3K15 | ENSG00000180815.15 | transcript | ENST00000338883.9 | protein_coding | 7/28 | chrX | TogoVar | ||||||
MAP3K15_chrX_19355059_19520508 | 19429822 | G | GAGAGAGA others(6): Show |
intron_variant | MODIFIER | NA19085.hp1 | a0018 | a0018c0025 | a0018c0025t0004 | a0018c0025t0004g0017 | 1 | 163 | 0.0061 | 13 | c.116 others(32): Show |
MAP3K15 | ENSG00000180815.15 | transcript | ENST00000338883.9 | protein_coding | 7/28 | chrX | TogoVar | ||||||
MAP3K15_chrX_19355059_19520508 | 19447883 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG01081.hp2 | a0002 | a0002c0017 | a0002c0017t0002 | a0002c0017t0002g0145 | 1 | 163 | 0.0061 | 13 | c.995 others(30): Show |
MAP3K15 | ENSG00000180815.15 | transcript | ENST00000338883.9 | protein_coding | 6/28 | chrX | TogoVar | ||||||
MAP3K15_chrX_19355059_19520508 | 19482179 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG02809.hp2 HG03486.hp1 |
a0002 | a0002c0002 | a0002c0002t0003a0002c0002t0021 | a0002c0002t0003g0026a0002c0002t0021g0162 | 2 | 163 | 0.0123 | 13 | c.525 others(30): Show |
MAP3K15 | ENSG00000180815.15 | transcript | ENST00000338883.9 | protein_coding | 3/28 | chrX | TogoVar | ||||||
MAP3K15_chrX_19355059_19520508 | 19494878 | T | TAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG02559.hp1 HG02895.hp1 HG03239.hp1 |
a0002a0004a0017 | a0002c0003a0004c0005a0017c0024 | a0002c0003t0019a0004c0005t0010a0017c0024t0006 | a0002c0003t0019g0152a0004c0005t0010g0009a0017c0024t0006g0160 | 3 | 163 | 0.0184 | 13 | c.362 others(30): Show |
MAP3K15 | ENSG00000180815.15 | transcript | ENST00000338883.9 | protein_coding | 1/28 | chrX | TogoVar | ||||||
MAP3K20_chr2_173070846_173273015 | 173085784 | A | ATTTTTTT others(6): Show |
intron_variant | MODIFIER | NA18945.hp2 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0118 | 1 | 334 | 0.0030 | 13 | c.-34 others(30): Show |
MAP3K20 | ENSG00000091436.17 | transcript | ENST00000375213.8 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MAP3K20_chr2_173070846_173273015 | 173134424 | A | ATTTTTTT others(6): Show |
intron_variant | MODIFIER | HG02015.hp2 | a0001 | a0001c0019 | a0001c0019t0001 | a0001c0019t0001g0240 | 1 | 334 | 0.0030 | 13 | c.160 others(32): Show |
MAP3K20 | ENSG00000091436.17 | transcript | ENST00000375213.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MAP3K20_chr2_173070846_173273015 | 173134426 | A | ATTTTTTT others(6): Show |
intron_variant | MODIFIER | HG03225.hp2 NA19066.hp1 |
a0001 | a0001c0004a0001c0012 | a0001c0004t0002a0001c0012t0007 | a0001c0004t0002g0096a0001c0012t0007g0119 | 2 | 334 | 0.0060 | 13 | c.160 others(32): Show |
MAP3K20 | ENSG00000091436.17 | transcript | ENST00000375213.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MAP3K20_chr2_173070846_173273015 | 173134428 | A | ATATATTT others(6): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0006 | a0006c0018 | a0006c0018t0011 | a0006c0018t0011g0251 | 1 | 334 | 0.0030 | 13 | c.160 others(32): Show |
MAP3K20 | ENSG00000091436.17 | transcript | ENST00000375213.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MAP3K20_chr2_173070846_173273015 | 173134428 | A | ATATTTTT others(6): Show |
intron_variant | MODIFIER | NA18974.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0227 | 1 | 334 | 0.0030 | 13 | c.160 others(32): Show |
MAP3K20 | ENSG00000091436.17 | transcript | ENST00000375213.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MAP3K20_chr2_173070846_173273015 | 173134428 | A | ATTTTTTT others(6): Show |
intron_variant | MODIFIER | HG02129.hp2 HG02135.hp1 NA18944.hp2 others(1): Show |
a0002a0007 | a0002c0003a0007c0017 | a0002c0003t0003a0007c0017t0001 | a0002c0003t0003g0210a0002c0003t0003g0221a0002c0003t0003g0223others(1): Show | 4 | 334 | 0.0120 | 13 | c.160 others(32): Show |
MAP3K20 | ENSG00000091436.17 | transcript | ENST00000375213.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MAP3K20_chr2_173070846_173273015 | 173159348 | T | TCTTTCTT others(6): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(232): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0004others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(32): Show | a0001c0001t0001g0006a0001c0001t0001g0057a0001c0001t0001g0081others(231): Show | 235 | 334 | 0.7036 | 13 | c.160 others(32): Show |
MAP3K20 | ENSG00000091436.17 | transcript | ENST00000375213.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MAP3K20_chr2_173070846_173273015 | 173220067 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00642.hp2 HG00733.hp1 others(75): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0004a0001c0007others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(14): Show | a0001c0001t0001g0057a0001c0001t0002g0003a0001c0001t0002g0004others(75): Show | 78 | 334 | 0.2335 | 13 | c.987 others(30): Show |
MAP3K20 | ENSG00000091436.17 | transcript | ENST00000375213.8 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MAP3K2_chr2_127293668_127392975 | 127296002 | A | AAAAAAAA others(6): Show |
downstream_gene_variant | MODIFIER | NA18522.hp2 | a0001 | a0001c0001 | a0001c0001t0025 | a0001c0001t0025g0318 | 1 | 320 | 0.0031 | 13 | c.*11 others(26): Show |
MAP3K2 | ENSG00000169967.17 | transcript | ENST00000682094.1 | protein_coding | 2665 | chr2 | TogoVar | ||||||
MAP3K4_chr6_160986769_161122380 | 160990208 | C | CCGCATGC others(6): Show |
upstream_gene_variant | MODIFIER | NA19076.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0112 | 1 | 342 | 0.0029 | 13 | c.-17 others(24): Show |
MAP3K4 | ENSG00000085511.20 | transcript | ENST00000392142.9 | protein_coding | 1560 | chr6 | TogoVar | ||||||
MAP3K5_chr6_136552046_136797477 | 136759482 | A | ATATATAT others(6): Show |
intron_variant | MODIFIER | HG01978.hp1 HG01978.hp2 |
a0001 | a0001c0002a0001c0007 | a0001c0002t0001a0001c0007t0002 | a0001c0002t0001g0042a0001c0007t0002g0011 | 2 | 162 | 0.0124 | 13 | c.448 others(32): Show |
MAP3K5 | ENSG00000197442.11 | transcript | ENST00000359015.5 | protein_coding | 1/29 | chr6 | TogoVar | ||||||
MAP3K8_chr10_30429184_30466833 | 30432976 | G | GAGAGAGA others(6): Show |
upstream_gene_variant | MODIFIER | HG00733.hp1 HG01993.hp1 NA18984.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0006 | a0001c0001t0001g0101a0001c0002t0001g0004a0002c0004t0006g0036others(2): Show | 5 | 386 | 0.0130 | 13 | c.-16 others(24): Show |
MAP3K8 | ENSG00000107968.10 | transcript | ENST00000263056.6 | protein_coding | 1207 | chr10 | TogoVar | ||||||
MAP3K8_chr10_30429184_30466833 | 30432978 | G | GAGAGAGA others(6): Show |
upstream_gene_variant | MODIFIER | HG01884.hp2 HG02896.hp2 HG03139.hp1 others(1): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(1): Show | a0001c0001t0001g0011a0001c0001t0003g0061a0001c0001t0011g0074others(1): Show | 4 | 386 | 0.0104 | 13 | c.-16 others(24): Show |
MAP3K8 | ENSG00000107968.10 | transcript | ENST00000263056.6 | protein_coding | 1205 | chr10 | TogoVar | ||||||
MAP3K9_chr14_70717526_70814513 | 70764192 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
a0001a0002a0005others(5): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(63): Show | a0001c0001t0002g0026a0001c0001t0002g0028a0001c0001t0002g0029others(154): Show | 164 | 374 | 0.4385 | 13 | c.821 others(30): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | TogoVar | ||||||
MAP3K9_chr14_70717526_70814513 | 70794990 | C | CTTTTTTT others(6): Show |
intron_variant | MODIFIER | HG01891.hp1 HG02074.hp1 HG02895.hp2 others(3): Show |
a0001a0007 | a0001c0001a0001c0003a0007c0015 | a0001c0001t0007a0001c0001t0012a0001c0001t0088others(3): Show | a0001c0001t0007g0270a0001c0001t0012g0031a0001c0001t0088g0254others(3): Show | 6 | 374 | 0.0160 | 13 | c.820 others(30): Show |
MAP3K9 | ENSG00000006432.16 | transcript | ENST00000554752.7 | protein_coding | 2/11 | chr14 | TogoVar | ||||||
MAP4K1_chr19_38582641_38622953 | 38590386 | A | ATATATAT others(6): Show |
intron_variant | MODIFIER | NA18964.hp2 | a0005 | a0005c0010 | a0005c0010t0001 | a0005c0010t0001g0293 | 1 | 348 | 0.0029 | 13 | c.239 others(32): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | TogoVar | ||||||
MAP4K1_chr19_38582641_38622953 | 38590390 | A | ATATATAT others(6): Show |
intron_variant | MODIFIER | NA19077.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0160 | 1 | 348 | 0.0029 | 13 | c.239 others(32): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | TogoVar | ||||||
MAP4K1_chr19_38582641_38622953 | 38608828 | A | AAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG00621.hp2 HG01243.hp2 HG02300.hp2 others(1): Show |
a0001a0006 | a0001c0001a0006c0012 | a0001c0001t0001a0006c0012t0001 | a0001c0001t0001g0202a0001c0001t0001g0205a0001c0001t0001g0331others(1): Show | 4 | 348 | 0.0115 | 13 | c.100 others(30): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 13/30 | chr19 | TogoVar | ||||||
MAP4K3_chr2_39244266_39442285 | 39369193 | G | GTTTTTTT others(6): Show |
intron_variant | MODIFIER | HG02622.hp2 HG02922.hp1 HG03579.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0014a0001c0001t0015 | a0001c0001t0003g0173a0001c0001t0003g0190a0001c0001t0014g0189others(1): Show | 4 | 232 | 0.0172 | 13 | c.154 others(30): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | TogoVar | ||||||
MAP4K3_chr2_39244266_39442285 | 39369205 | G | GTTTTTTG others(6): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00738.hp1 HG01081.hp1 others(17): Show |
a0001a0004 | a0001c0001a0001c0003a0004c0009 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(2): Show | a0001c0001t0002g0052a0001c0001t0002g0053a0001c0001t0002g0054others(17): Show | 20 | 232 | 0.0862 | 13 | c.154 others(30): Show |
MAP4K3 | ENSG00000011566.15 | transcript | ENST00000263881.8 | protein_coding | 2/33 | chr2 | TogoVar |