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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
MAOB_chrX_43761610_43887450 | 43857112 | TATATAGA others(19): Show |
T | intron_variant | MODIFIER | HG00735.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0067 | 1 | 234 | 0.0043 | -26 | c.47- others(43): Show |
MAOB | ENSG00000069535.14 | transcript | ENST00000378069.5 | protein_coding | 1/14 | chrX | TogoVar | ||||||
MAP1B_chr5_72102475_72214565 | 72178725 | GGTGTGTG others(19): Show |
G | intron_variant | MODIFIER | HG03041.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0337 | 1 | 342 | 0.0029 | -26 | c.287 others(43): Show |
MAP1B | ENSG00000131711.15 | transcript | ENST00000296755.12 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
MAP1LC3B2_chr12_116554381_116581606 | 116560188 | CTATATAT others(19): Show |
C | intron_variant | MODIFIER | HG02155.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0391 | 1 | 446 | 0.0022 | -26 | c.-10 others(43): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
MAP1LC3B2_chr12_116554381_116581606 | 116566930 | CAAAAAAA others(19): Show |
C | intron_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0351 | 1 | 446 | 0.0022 | -26 | c.-10 others(45): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
MAP2K1_chr15_66381912_66496544 | 66421083 | TACACACA others(19): Show |
T | intron_variant | MODIFIER | HG02615.hp1 NA19240.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0339a0001c0001t0001g0340 | 2 | 372 | 0.0054 | -26 | c.81- others(43): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
MAP2K2_chr19_4085321_4129122 | 4123546 | TCCGAGGG others(19): Show |
T | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(59): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0048a0001c0001t0001g0051a0001c0001t0001g0054others(58): Show | 62 | 330 | 0.1879 | -26 | c.92+ others(39): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | TogoVar | ||||||
MAP2K4_chr17_12015877_12148828 | 12069890 | CATATATA others(19): Show |
C | intron_variant | MODIFIER | HG00280.hp2 HG01081.hp1 HG02071.hp2 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(11): Show | 14 | 322 | 0.0435 | -26 | c.219 others(45): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
MAP2K4_chr17_12015877_12148828 | 12088542 | TTATATCT others(19): Show |
T | intron_variant | MODIFIER | homoSapiens_chm13v2.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0205 | 1 | 322 | 0.0031 | -26 | c.393 others(43): Show |
MAP2K4 | ENSG00000065559.15 | transcript | ENST00000353533.10 | protein_coding | 3/10 | chr17 | TogoVar | ||||||
MAP2K5_chr15_67537703_67812114 | 67634367 | CAAAAAAA others(19): Show |
C | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(42): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0174a0001c0001t0001g0196a0001c0001t0001g0198others(42): Show | 45 | 278 | 0.1619 | -26 | c.585 others(43): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
MAP2K5_chr15_67537703_67812114 | 67714413 | GGAAAAAA others(19): Show |
G | intron_variant | MODIFIER | HG02559.hp1 HG02717.hp2 HG02976.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(1): Show | 4 | 278 | 0.0144 | -26 | c.104 others(47): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 16/21 | chr15 | TogoVar | ||||||
MAP2K5_chr15_67537703_67812114 | 67739440 | ATATATAT others(19): Show |
A | intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0087 | 1 | 278 | 0.0036 | -26 | c.107 others(45): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
MAP2K5_chr15_67537703_67812114 | 67739442 | ATATATAT others(19): Show |
A | intron_variant | MODIFIER | HG02027.hp2 HG02698.hp2 NA18965.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0006 | a0001c0001t0003g0031a0001c0001t0003g0035a0001c0001t0006g0277 | 3 | 278 | 0.0108 | -26 | c.107 others(45): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
MAP2K5_chr15_67537703_67812114 | 67739444 | ATATATAT others(19): Show |
A | intron_variant | MODIFIER | HG00323.hp1 HG00558.hp2 HG01123.hp1 others(32): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(1): Show | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0146others(32): Show | 35 | 278 | 0.1259 | -26 | c.107 others(45): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
MAP2K5_chr15_67537703_67812114 | 67739446 | ATATATAT others(19): Show |
A | intron_variant | MODIFIER | HG00597.hp1 HG00621.hp1 HG01884.hp1 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0196a0001c0001t0001g0198a0001c0001t0002g0141others(12): Show | 15 | 278 | 0.0540 | -26 | c.107 others(45): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
MAP2K5_chr15_67537703_67812114 | 67739448 | ATATATAT others(19): Show |
A | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp1 HG02622.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0004 | a0001c0001t0002g0144a0001c0001t0002g0149a0001c0001t0002g0150others(5): Show | 8 | 278 | 0.0288 | -26 | c.107 others(45): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
MAP2K5_chr15_67537703_67812114 | 67739450 | ATATATAT others(19): Show |
A | intron_variant | MODIFIER | HG02258.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0148 | 1 | 278 | 0.0036 | -26 | c.107 others(45): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
MAP2K5_chr15_67537703_67812114 | 67739452 | ATATATAT others(19): Show |
A | intron_variant | MODIFIER | HG04228.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0202 | 1 | 278 | 0.0036 | -26 | c.107 others(45): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
MAP2K5_chr15_67537703_67812114 | 67739454 | ATATATAT others(19): Show |
A | intron_variant | MODIFIER | NA18967.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0204 | 1 | 278 | 0.0036 | -26 | c.107 others(45): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
MAP2K5_chr15_67537703_67812114 | 67739456 | ATATATAT others(19): Show |
A | intron_variant | MODIFIER | NA18973.hp1 NA18991.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0177a0001c0001t0001g0179 | 2 | 278 | 0.0072 | -26 | c.107 others(45): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
MAP2K5_chr15_67537703_67812114 | 67739458 | ATATATTT others(19): Show |
A | intron_variant | MODIFIER | HG02572.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0200 | 1 | 278 | 0.0036 | -26 | c.107 others(45): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
MAP2K6_chr17_69409697_69558865 | 69449545 | CTTTCTTT others(19): Show |
C | intron_variant | MODIFIER | HG02258.hp2 | a0001 | a0001c0001 | a0001c0001t0028 | a0001c0001t0028g0112 | 1 | 260 | 0.0039 | -26 | c.16+ others(43): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
MAP2K6_chr17_69409697_69558865 | 69498001 | TGCTTGTA others(19): Show |
T | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(40): Show | a0001c0001t0001g0186a0001c0001t0001g0195a0001c0001t0001g0217others(107): Show | 110 | 260 | 0.4231 | -26 | c.17- others(41): Show |
MAP2K6 | ENSG00000108984.16 | transcript | ENST00000590474.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
MAP2_chr2_209419047_209739112 | 209528771 | TATGTACA others(19): Show |
T | intron_variant | MODIFIER | HG01243.hp2 HG02451.hp2 |
a0004 | a0004c0007 | a0004c0007t0017 | a0004c0007t0017g0058a0004c0007t0017g0147 | 2 | 148 | 0.0135 | -26 | c.-17 others(47): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MAP2_chr2_209419047_209739112 | 209528797 | CATGTACA others(19): Show |
C | intron_variant | MODIFIER | HG00597.hp2 | a0001 | a0001c0017 | a0001c0017t0007 | a0001c0017t0007g0036 | 1 | 148 | 0.0068 | -26 | c.-17 others(47): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MAP2_chr2_209419047_209739112 | 209676720 | CATATATA others(19): Show |
C | intron_variant | MODIFIER | HG00140.hp2 HG00408.hp2 HG01109.hp1 others(24): Show |
a0001a0006a0009others(1): Show | a0001c0001a0006c0018a0009c0019others(1): Show | a0001c0001t0001a0001c0001t0002a0006c0018t0001others(2): Show | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0012others(24): Show | 27 | 148 | 0.1824 | -26 | c.263 others(43): Show |
MAP2 | ENSG00000078018.22 | transcript | ENST00000682079.1 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MAP3K12_chr12_53474669_53504458 | 53498908 | CTGTGTGT others(19): Show |
C | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG01070.hp1 others(13): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(3): Show | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0075others(11): Show | 16 | 328 | 0.0488 | -26 | c.-38 others(41): Show |
MAP3K12 | ENSG00000139625.13 | transcript | ENST00000547488.6 | protein_coding | 1/13 | chr12 | TogoVar | ||||||
MAP3K13_chr3_185358136_185494094 | 185453958 | GATATATA others(19): Show |
G | intron_variant | MODIFIER | HG01081.hp2 HG01981.hp1 HG02074.hp1 others(19): Show |
a0001a0002a0009 | a0001c0001a0002c0005a0009c0017 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(5): Show | a0001c0001t0001g0251a0001c0001t0002g0018a0001c0001t0002g0019others(19): Show | 22 | 278 | 0.0791 | -26 | c.127 others(45): Show |
MAP3K13 | ENSG00000073803.14 | transcript | ENST00000265026.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
MAP3K15_chrX_19355059_19520508 | 19429760 | AAGAGAGA others(19): Show |
A | intron_variant | MODIFIER | HG02258.hp1 HG02630.hp1 HG03453.hp1 |
a0002 | a0002c0002 | a0002c0002t0003a0002c0002t0005 | a0002c0002t0003g0136a0002c0002t0003g0137a0002c0002t0005g0019 | 3 | 163 | 0.0184 | -26 | c.116 others(45): Show |
MAP3K15 | ENSG00000180815.15 | transcript | ENST00000338883.9 | protein_coding | 7/28 | chrX | TogoVar | ||||||
MAP3K15_chrX_19355059_19520508 | 19476716 | CGGTGCCA others(19): Show |
C | intron_variant | MODIFIER | HG02897.hp1 | a0005 | a0005c0007 | a0005c0007t0003 | a0005c0007t0003g0129 | 1 | 163 | 0.0061 | -26 | c.525 others(43): Show |
MAP3K15 | ENSG00000180815.15 | transcript | ENST00000338883.9 | protein_coding | 3/28 | chrX | TogoVar | ||||||
MAP3K20_chr2_173070846_173273015 | 173110219 | ATATATAT others(19): Show |
A | intron_variant | MODIFIER | NA18948.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0273 | 1 | 334 | 0.0030 | -26 | c.159 others(45): Show |
MAP3K20 | ENSG00000091436.17 | transcript | ENST00000375213.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MAP3K20_chr2_173070846_173273015 | 173168072 | ATTATTTC others(19): Show |
A | intron_variant | MODIFIER | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(57): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0007a0001c0019others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(9): Show | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0225others(57): Show | 60 | 334 | 0.1796 | -26 | c.160 others(43): Show |
MAP3K20 | ENSG00000091436.17 | transcript | ENST00000375213.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
MAP3K2_chr2_127293668_127392975 | 127378869 | CAATCCTC others(19): Show |
C | intron_variant | MODIFIER | NA19082.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0250 | 1 | 320 | 0.0031 | -26 | c.-66 others(43): Show |
MAP3K2 | ENSG00000169967.17 | transcript | ENST00000682094.1 | protein_coding | 1/16 | chr2 | TogoVar | ||||||
MAP4K1_chr19_38582641_38622953 | 38590388 | AAAAAAAA others(19): Show |
A | intron_variant | MODIFIER | HG01358.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0157 | 1 | 348 | 0.0029 | -26 | c.239 others(45): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 30/30 | chr19 | TogoVar | ||||||
MAP4K1_chr19_38582641_38622953 | 38602680 | ATATACAT others(19): Show |
A | intron_variant | MODIFIER | HG02145.hp1 HG02886.hp1 HG02895.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0152 | 3 | 348 | 0.0086 | -26 | c.144 others(45): Show |
MAP4K1 | ENSG00000104814.13 | transcript | ENST00000396857.7 | protein_coding | 19/30 | chr19 | TogoVar | ||||||
MAP4K2_chr11_64779918_64808214 | 64795839 | TCTTGAAA others(19): Show |
T | intron_variant | MODIFIER | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0166a0001c0001t0004g0032a0001c0001t0004g0112 | 4 | 368 | 0.0109 | -26 | c.175 others(43): Show |
MAP4K2 | ENSG00000168067.12 | transcript | ENST00000294066.7 | protein_coding | 24/31 | chr11 | TogoVar | ||||||
MAP4K5_chr14_50413521_50537569 | 50441743 | TACACACA others(19): Show |
T | intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0151 | 1 | 240 | 0.0042 | -26 | c.156 others(43): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | TogoVar | ||||||
MAP4K5_chr14_50413521_50537569 | 50441773 | CACACACA others(19): Show |
C | intron_variant | MODIFIER | HG02258.hp1 HG02572.hp2 HG02647.hp1 others(1): Show |
a0001 | a0001c0006 | a0001c0006t0001a0001c0006t0010 | a0001c0006t0001g0231a0001c0006t0001g0232a0001c0006t0001g0233others(1): Show | 4 | 240 | 0.0167 | -26 | c.156 others(43): Show |
MAP4K5 | ENSG00000012983.12 | transcript | ENST00000682126.1 | protein_coding | 21/32 | chr14 | TogoVar | ||||||
MAP4_chr3_47845695_48021416 | 47854720 | AGCCCTGC others(19): Show |
A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(123): Show |
a0002a0003a0004others(18): Show | a0002c0002a0002c0011a0002c0020others(20): Show | a0002c0002t0002a0002c0002t0004a0002c0002t0006others(30): Show | a0002c0002t0002g0001a0002c0002t0002g0004a0002c0002t0002g0005others(122): Show | 126 | 232 | 0.5431 | -26 | c.669 others(43): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 19/20 | chr3 | TogoVar | ||||||
MAP4_chr3_47845695_48021416 | 47881446 | CTATATAT others(19): Show |
C | intron_variant | MODIFIER | HG02922.hp2 | a0012 | a0012c0013 | a0012c0013t0011 | a0012c0013t0011g0222 | 1 | 232 | 0.0043 | -26 | c.543 others(45): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 10/20 | chr3 | TogoVar | ||||||
MAP4_chr3_47845695_48021416 | 47966228 | CTTTTTTT others(19): Show |
C | intron_variant | MODIFIER | HG02735.hp2 | a0016 | a0016c0029 | a0016c0029t0016 | a0016c0029t0016g0155 | 1 | 232 | 0.0043 | -26 | c.292 others(45): Show |
MAP4 | ENSG00000047849.22 | transcript | ENST00000683076.1 | protein_coding | 3/20 | chr3 | TogoVar | ||||||
MAP6D1_chr3_183810922_183830577 | 183822240 | AACACACA others(19): Show |
A | intron_variant | MODIFIER | HG01243.hp1 HG01978.hp2 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004 | a0001c0001t0003g0130a0001c0001t0004g0131 | 2 | 462 | 0.0043 | -26 | c.401 others(43): Show |
MAP6D1 | ENSG00000180834.8 | transcript | ENST00000318631.8 | protein_coding | 1/2 | chr3 | TogoVar | ||||||
MAP7D1_chr1_36151160_36185849 | 36175087 | ACCAGGTC others(19): Show |
A | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp2 HG00673.hp1 others(75): Show |
a0001a0005a0006others(3): Show | a0001c0001a0001c0024a0005c0007others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(9): Show | a0001c0001t0001g0047a0001c0001t0002g0001a0001c0001t0002g0006others(50): Show | 78 | 378 | 0.2064 | -26 | c.850 others(40): Show |
MAP7D1 | ENSG00000116871.16 | transcript | ENST00000474796.2 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
MAP7_chr6_136337734_136555422 | 136505267 | GTGTGTGT others(19): Show |
G | intron_variant | MODIFIER | HG02965.hp2 NA21309.hp1 |
a0008 | a0008c0008 | a0008c0008t0006 | a0008c0008t0006g0026a0008c0008t0006g0027 | 2 | 248 | 0.0081 | -26 | c.67+ others(43): Show |
MAP7 | ENSG00000135525.19 | transcript | ENST00000354570.8 | protein_coding | 1/17 | chr6 | TogoVar | ||||||
MAPK1_chr22_21754657_21872645 | 21814805 | TGGGCGAC others(19): Show |
T | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp2 HG02970.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0027 | a0001c0001t0001g0265a0001c0001t0001g0267a0001c0001t0001g0271others(1): Show | 4 | 348 | 0.0115 | -26 | c.120 others(43): Show |
MAPK1 | ENSG00000100030.15 | transcript | ENST00000215832.11 | protein_coding | 1/8 | chr22 | TogoVar | ||||||
MAPK1_chr22_21754657_21872645 | 21814854 | CAGAGAGA others(19): Show |
C | intron_variant | MODIFIER | HG02109.hp1 HG02145.hp2 HG02622.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0056 | a0001c0001t0008g0025a0001c0001t0008g0026a0001c0001t0008g0030others(5): Show | 8 | 348 | 0.0230 | -26 | c.120 others(43): Show |
MAPK1 | ENSG00000100030.15 | transcript | ENST00000215832.11 | protein_coding | 1/8 | chr22 | TogoVar | ||||||
MAPK6_chr15_52014219_52072375 | 52053626 | GGTTGATT others(19): Show |
G | intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0001 | a0001c0001t0041 | a0001c0001t0041g0262 | 1 | 356 | 0.0028 | -26 | c.700 others(43): Show |
MAPK6 | ENSG00000069956.14 | transcript | ENST00000261845.7 | protein_coding | 3/5 | chr15 | TogoVar | ||||||
MAPKAPK5_chr12_111837228_111907222 | 111906406 | GCCAAAGG others(19): Show |
G | downstream_gene_variant | MODIFIER | HG02965.hp1 | a0001 | a0001c0001 | a0001c0001t0018 | a0001c0001t0018g0141 | 1 | 352 | 0.0028 | -26 | c.*13 others(39): Show |
MAPKAPK5 | ENSG00000089022.15 | transcript | ENST00000550735.7 | protein_coding | 4185 | chr12 | TogoVar | ||||||
MAPT_chr17_45889554_46033334 | 45904222 | ATATATAT others(19): Show |
A | intron_variant | MODIFIER | HG01167.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0193 | 1 | 253 | 0.0040 | -26 | c.-18 others(43): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
MAPT_chr17_45889554_46033334 | 45956548 | TTATATAT others(19): Show |
T | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp2 HG00642.hp1 others(23): Show |
a0001a0002a0004others(5): Show | a0001c0001a0002c0003a0004c0005others(5): Show | a0001c0001t0002a0001c0001t0007a0001c0001t0010others(9): Show | a0001c0001t0002g0031a0001c0001t0002g0046a0001c0001t0002g0047others(23): Show | 26 | 253 | 0.1028 | -26 | c.-17 others(43): Show |
MAPT | ENSG00000186868.18 | transcript | ENST00000262410.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
MARCHF1_chr4_163519718_164389019 | 163847549 | CTTTTTTT others(19): Show |
C | intron_variant | MODIFIER | HG02055.hp2 NA18972.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0005a0001c0002t0002 | a0001c0001t0005g0029a0001c0002t0002g0097 | 2 | 102 | 0.0196 | -26 | c.111 others(43): Show |
MARCHF1 | ENSG00000145416.14 | transcript | ENST00000514618.6 | protein_coding | 4/9 | chr4 | TogoVar |