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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
MAN1C1_chr1_25611791_25789450 | 25644518 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG01071.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0231 | 1 | 250 | 0.0040 | 30 | c.540 others(49): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
MAN1C1_chr1_25611791_25789450 | 25644518 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG02895.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0232 | 1 | 250 | 0.0040 | 30 | c.540 others(49): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
MAN1C1_chr1_25611791_25789450 | 25656095 | C | CTTTTTTT others(23): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0229 | 1 | 250 | 0.0040 | 30 | c.541 others(49): Show |
MAN1C1 | ENSG00000117643.16 | transcript | ENST00000374332.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
MAN2A1_chr5_109684927_109874625 | 109708509 | G | GACACACA others(23): Show |
intron_variant | MODIFIER | HG00733.hp2 HG01981.hp1 HG02074.hp1 others(5): Show |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0009 | a0002c0002t0002g0178 a0002c0002t0002g0229 a0002c0002t0002g0241 others(5): Show |
8 | 296 | 0.0270 | 30 | c.136 others(47): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
MAN2A1_chr5_109684927_109874625 | 109817172 | A | ATATATGT others(23): Show |
intron_variant | MODIFIER | HG01192.hp1 HG04228.hp2 |
a0001 | a0001c0004 | a0001c0004t0013 | a0001c0004t0013g0214 a0001c0004t0013g0282 |
2 | 296 | 0.0068 | 30 | c.194 others(45): Show |
MAN2A1 | ENSG00000112893.10 | transcript | ENST00000261483.5 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
MAN2B2_chr4_6570189_6628362 | 6579289 | T | TCACCACC others(23): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0002 | a0002c0030 | a0002c0030t0013 | a0002c0030t0013g0136 | 1 | 362 | 0.0028 | 30 | c.391 others(45): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
MAN2B2_chr4_6570189_6628362 | 6579307 | C | CCACCACC others(23): Show |
intron_variant | MODIFIER | HG02976.hp1 | a0002 | a0002c0002 | a0002c0002t0009 | a0002c0002t0009g0025 | 1 | 362 | 0.0028 | 30 | c.391 others(45): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
MANBA_chr4_102625770_102765968 | 102625838 | A | AATTTTAT others(23): Show |
downstream_gene_variant | MODIFIER | HG03486.hp1 HG03516.hp1 |
a0003 | a0003c0005 | a0003c0005t0021 | a0003c0005t0021g0251 a0003c0005t0021g0252 |
2 | 280 | 0.0071 | 30 | c.*62 others(41): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 4931 | chr4 | TogoVar | |||||||
MANBA_chr4_102625770_102765968 | 102747158 | G | GATATATA others(23): Show |
intron_variant | MODIFIER | HG02615.hp1 HG02965.hp1 HG03471.hp1 |
a0001a0009 | a0001c0004a0001c0009a0009c0011 | a0001c0004t0012a0001c0009t0034a0009c0011t0029 | a0001c0004t0012g0253 a0001c0009t0034g0016 a0009c0011t0029g0018 |
3 | 280 | 0.0107 | 30 | c.177 others(49): Show |
MANBA | ENSG00000109323.11 | transcript | ENST00000647097.2 | protein_coding | 1/16 | chr4 | TogoVar | |||||||
MAOA_chrX_43651299_43751817 | 43655100 | C | CACCGGCA others(23): Show |
upstream_gene_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(106): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0005others(8): Show | a0001c0001t0001g0156 a0001c0001t0001g0159 a0001c0001t0001g0247 others(102): Show |
109 | 283 | 0.3852 | 30 | c.-12 others(41): Show |
MAOA | ENSG00000189221.11 | transcript | ENST00000338702.4 | protein_coding | 1198 | chrX | TogoVar | |||||||
MAOA_chrX_43651299_43751817 | 43655140 | G | GGCACCAG others(23): Show |
upstream_gene_variant | MODIFIER | HG02735.hp1 HG03704.hp1 homoSapiens_chm13v2.hp1 |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0006 | a0001c0002t0002g0168 a0001c0002t0002g0172 a0001c0002t0006g0165 |
3 | 283 | 0.0106 | 30 | c.-12 others(41): Show |
MAOA | ENSG00000189221.11 | transcript | ENST00000338702.4 | protein_coding | 1158 | chrX | TogoVar | |||||||
MAOA_chrX_43651299_43751817 | 43655177 | G | GTACCCGC others(23): Show |
upstream_gene_variant | MODIFIER | HG01891.hp2 HG03195.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0002 | a0001c0001t0001g0243 a0001c0003t0002g0238 |
2 | 283 | 0.0071 | 30 | c.-11 others(41): Show |
MAOA | ENSG00000189221.11 | transcript | ENST00000338702.4 | protein_coding | 1121 | chrX | TogoVar | |||||||
MAP1LC3B2_chr12_116554381_116581606 | 116560228 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG02559.hp1 NA20300.hp1 |
a0002 | a0002c0002 | a0002c0002t0016 | a0002c0002t0016g0037 a0002c0002t0016g0038 |
2 | 446 | 0.0045 | 30 | c.-10 others(47): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
MAP2K1_chr15_66381912_66496544 | 66416181 | T | TAGGGAGT others(23): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0216 | 1 | 372 | 0.0027 | 30 | c.81- others(47): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MAP2K1_chr15_66381912_66496544 | 66420721 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG01891.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0361 | 1 | 372 | 0.0027 | 30 | c.81- others(47): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MAP2K1_chr15_66381912_66496544 | 66420721 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG01109.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0359 | 1 | 372 | 0.0027 | 30 | c.81- others(47): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MAP2K1_chr15_66381912_66496544 | 66420721 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG02559.hp2 NA18906.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0364 a0001c0001t0001g0370 |
2 | 372 | 0.0054 | 30 | c.81- others(47): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MAP2K1_chr15_66381912_66496544 | 66420721 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0342 | 1 | 372 | 0.0027 | 30 | c.81- others(47): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MAP2K1_chr15_66381912_66496544 | 66420779 | G | GTATATAT others(23): Show |
intron_variant | MODIFIER | HG02615.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0339 | 1 | 372 | 0.0027 | 30 | c.81- others(47): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MAP2K1_chr15_66381912_66496544 | 66469693 | G | GACACACA others(23): Show |
intron_variant | MODIFIER | HG01934.hp1 HG02258.hp1 NA18941.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0103 a0001c0001t0001g0112 a0001c0001t0001g0133 others(1): Show |
4 | 372 | 0.0108 | 30 | c.569 others(49): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MAP2K1_chr15_66381912_66496544 | 66469723 | C | CACACACA others(23): Show |
intron_variant | MODIFIER | HG03669.hp1 NA18949.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0005 | a0001c0001t0002g0060 a0001c0001t0005g0158 |
2 | 372 | 0.0054 | 30 | c.569 others(49): Show |
MAP2K1 | ENSG00000169032.11 | transcript | ENST00000307102.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MAP2K2_chr19_4085321_4129122 | 4085812 | A | ATAATGGC others(23): Show |
downstream_gene_variant | MODIFIER | HG02738.hp2 | a0001 | a0001c0005 | a0001c0005t0003 | a0001c0005t0003g0081 | 1 | 330 | 0.0030 | 30 | c.*47 others(41): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4508 | chr19 | TogoVar | |||||||
MAP2K2_chr19_4085321_4129122 | 4085812 | A | ATATTGGC others(23): Show |
downstream_gene_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(257): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0028 others(243): Show |
260 | 330 | 0.7879 | 30 | c.*47 others(41): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4508 | chr19 | TogoVar | |||||||
MAP2K2_chr19_4085321_4129122 | 4085833 | C | CGTCTCCT others(23): Show |
downstream_gene_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0280 | 1 | 330 | 0.0030 | 30 | c.*47 others(41): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 4487 | chr19 | TogoVar | |||||||
MAP2K2_chr19_4085321_4129122 | 4122277 | G | GACCCTCC others(23): Show |
intron_variant | MODIFIER | HG01433.hp1 HG02165.hp2 NA18943.hp2 others(5): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0008 | a0001c0001t0002a0001c0002t0001a0002c0008t0001 | a0001c0001t0002g0222 a0001c0002t0001g0194 a0001c0002t0001g0204 others(5): Show |
8 | 330 | 0.0242 | 30 | c.92+ others(45): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | TogoVar | |||||||
MAP2K2_chr19_4085321_4129122 | 4122333 | T | TAGGGACC others(23): Show |
intron_variant | MODIFIER | HG00408.hp2 HG00639.hp1 HG01070.hp1 others(14): Show |
a0001a0003 | a0001c0005a0001c0006a0001c0011others(1): Show | a0001c0005t0001a0001c0005t0003a0001c0006t0001others(2): Show | a0001c0005t0001g0145 a0001c0005t0003g0001 a0001c0005t0003g0076 others(11): Show |
17 | 330 | 0.0515 | 30 | c.92+ others(45): Show |
MAP2K2 | ENSG00000126934.15 | transcript | ENST00000262948.10 | protein_coding | 1/10 | chr19 | TogoVar | |||||||
MAP2K3_chr17_21279711_21320232 | 21291262 | T | TCAATACA others(23): Show |
intron_variant | MODIFIER | HG00597.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0115 | 1 | 366 | 0.0027 | 30 | c.49+ others(45): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
MAP2K3_chr17_21279711_21320232 | 21291341 | T | TACAACAC others(23): Show |
intron_variant | MODIFIER | HG02647.hp2 NA18906.hp2 |
a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0251 a0001c0004t0001g0252 |
2 | 366 | 0.0055 | 30 | c.49+ others(45): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
MAP2K3_chr17_21279711_21320232 | 21291346 | T | TACAACAC others(23): Show |
intron_variant | MODIFIER | HG02723.hp2 | a0002 | a0002c0007 | a0002c0007t0009 | a0002c0007t0009g0256 | 1 | 366 | 0.0027 | 30 | c.49+ others(45): Show |
MAP2K3 | ENSG00000034152.20 | transcript | ENST00000342679.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
MAP2K5_chr15_67537703_67812114 | 67590468 | T | TCTCTCTC others(23): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00558.hp1 HG01109.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004 | a0001c0001t0001g0160 a0001c0001t0001g0169 a0001c0001t0001g0172 others(11): Show |
14 | 278 | 0.0504 | 30 | c.432 others(47): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MAP2K5_chr15_67537703_67812114 | 67609414 | A | ATAGACCT others(23): Show |
intron_variant | MODIFIER | HG02559.hp1 HG02647.hp1 HG02717.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(2): Show |
5 | 278 | 0.0180 | 30 | c.545 others(47): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MAP2K5_chr15_67537703_67812114 | 67609465 | A | ATAGATTC others(23): Show |
intron_variant | MODIFIER | HG02055.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0138 | 1 | 278 | 0.0036 | 30 | c.545 others(47): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MAP2K5_chr15_67537703_67812114 | 67609530 | T | TTCTGTAG others(23): Show |
intron_variant | MODIFIER | NA19087.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0094 | 1 | 278 | 0.0036 | 30 | c.545 others(47): Show |
MAP2K5 | ENSG00000137764.20 | transcript | ENST00000178640.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
MAP3K12_chr12_53474669_53504458 | 53498908 | C | CTGTGTGT others(23): Show |
intron_variant | MODIFIER | HG02965.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0056 | 1 | 328 | 0.0031 | 30 | c.-38 others(45): Show |
MAP3K12 | ENSG00000139625.13 | transcript | ENST00000547488.6 | protein_coding | 1/13 | chr12 | TogoVar | |||||||
MAP3K13_chr3_185358136_185494094 | 185454465 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | HG01515.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0258 | 1 | 278 | 0.0036 | 30 | c.127 others(49): Show |
MAP3K13 | ENSG00000073803.14 | transcript | ENST00000265026.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
MAP3K13_chr3_185358136_185494094 | 185483711 | C | CTTTTTTT others(23): Show |
3_prime_UTR_variant | MODIFIER | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(158): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(41): Show | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0038 others(158): Show |
161 | 278 | 0.5791 | 30 | c.*12 others(41): Show |
MAP3K13 | ENSG00000073803.14 | transcript | ENST00000265026.8 | protein_coding | 14/14 | 1271 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
MAP3K13_chr3_185358136_185494094 | 185483712 | T | TTTTTTTT others(23): Show |
3_prime_UTR_variant | MODIFIER | HG03491.hp1 HG03492.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0017a0001c0002t0017 | a0001c0001t0017g0112 a0001c0002t0017g0132 |
2 | 278 | 0.0072 | 30 | c.*12 others(41): Show |
MAP3K13 | ENSG00000073803.14 | transcript | ENST00000265026.8 | protein_coding | 14/14 | 1272 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
MAP3K13_chr3_185358136_185494094 | 185483713 | T | TTTTTTTT others(23): Show |
3_prime_UTR_variant | MODIFIER | HG02559.hp2 HG02976.hp2 |
a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0105 a0001c0001t0016g0212 |
2 | 278 | 0.0072 | 30 | c.*12 others(41): Show |
MAP3K13 | ENSG00000073803.14 | transcript | ENST00000265026.8 | protein_coding | 14/14 | 1271 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
MAP3K15_chrX_19355059_19520508 | 19477964 | A | AGGGAGAG others(23): Show |
intron_variant | MODIFIER | HG02486.hp1 | a0002 | a0002c0003 | a0002c0003t0003 | a0002c0003t0003g0128 | 1 | 163 | 0.0061 | 30 | c.525 others(47): Show |
MAP3K15 | ENSG00000180815.15 | transcript | ENST00000338883.9 | protein_coding | 3/28 | chrX | TogoVar | |||||||
MAP3K15_chrX_19355059_19520508 | 19478090 | G | GGGGGAGA others(23): Show |
intron_variant | MODIFIER | HG00673.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0056 | 1 | 163 | 0.0061 | 30 | c.525 others(47): Show |
MAP3K15 | ENSG00000180815.15 | transcript | ENST00000338883.9 | protein_coding | 3/28 | chrX | TogoVar | |||||||
MAP3K15_chrX_19355059_19520508 | 19478121 | G | GGAGAGGG others(23): Show |
intron_variant | MODIFIER | HG03486.hp1 | a0002 | a0002c0002 | a0002c0002t0021 | a0002c0002t0021g0162 | 1 | 163 | 0.0061 | 30 | c.525 others(47): Show |
MAP3K15 | ENSG00000180815.15 | transcript | ENST00000338883.9 | protein_coding | 3/28 | chrX | TogoVar | |||||||
MAP3K19_chr2_134959491_135052447 | 134997817 | C | CAAAAAAA others(23): Show |
intron_variant | MODIFIER | HG01978.hp1 HG02071.hp1 HG02738.hp1 others(2): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0002a0001c0002t0012 | a0001c0002t0001g0021 a0001c0002t0001g0121 a0001c0002t0001g0324 others(2): Show |
5 | 334 | 0.0150 | 30 | c.574 others(45): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 8/12 | chr2 | TogoVar | |||||||
MAP3K19_chr2_134959491_135052447 | 135048373 | A | ACACACTC others(23): Show |
upstream_gene_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0009 | a0001c0009t0002 | a0001c0009t0002g0133 | 1 | 334 | 0.0030 | 30 | c.-16 others(41): Show |
MAP3K19 | ENSG00000176601.14 | transcript | ENST00000392915.7 | protein_coding | 927 | chr2 | TogoVar | |||||||
MAP3K20_chr2_173070846_173273015 | 173134428 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG02004.hp1 NA18982.hp1 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0143 a0001c0001t0004g0177 |
2 | 334 | 0.0060 | 30 | c.160 others(49): Show |
MAP3K20 | ENSG00000091436.17 | transcript | ENST00000375213.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
MAP3K20_chr2_173070846_173273015 | 173134428 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG01261.hp1 HG01952.hp1 HG02148.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0009 | a0001c0001t0001g0006 a0001c0001t0004g0166 a0001c0001t0009g0155 |
3 | 334 | 0.0090 | 30 | c.160 others(49): Show |
MAP3K20 | ENSG00000091436.17 | transcript | ENST00000375213.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
MAP3K20_chr2_173070846_173273015 | 173134428 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG04228.hp2 | a0002 | a0002c0003 | a0002c0003t0003 | a0002c0003t0003g0173 | 1 | 334 | 0.0030 | 30 | c.160 others(49): Show |
MAP3K20 | ENSG00000091436.17 | transcript | ENST00000375213.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
MAP3K20_chr2_173070846_173273015 | 173134428 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG00735.hp1 HG03225.hp1 NA18980.hp1 |
a0001a0003 | a0001c0001a0003c0009 | a0001c0001t0001a0001c0001t0002a0003c0009t0005 | a0001c0001t0001g0057 a0001c0001t0002g0047 a0003c0009t0005g0091 |
3 | 334 | 0.0090 | 30 | c.160 others(49): Show |
MAP3K20 | ENSG00000091436.17 | transcript | ENST00000375213.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
MAP3K20_chr2_173070846_173273015 | 173134428 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG02895.hp1 HG03516.hp2 |
a0001 | a0001c0004 | a0001c0004t0002a0001c0004t0004 | a0001c0004t0002g0069 a0001c0004t0004g0066 |
2 | 334 | 0.0060 | 30 | c.160 others(49): 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(23): Show |
intron_variant | MODIFIER | NA19004.hp2 | a0003 | a0003c0005 | a0003c0005t0005 | a0003c0005t0005g0053 | 1 | 334 | 0.0030 | 30 | c.160 others(49): Show |
MAP3K20 | ENSG00000091436.17 | transcript | ENST00000375213.8 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
MAP3K2_chr2_127293668_127392975 | 127342388 | G | GGGGTGTG others(23): Show |
intron_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0001 | a0001c0001t0054 | a0001c0001t0054g0135 | 1 | 320 | 0.0031 | 30 | c.4+7 others(41): Show |
MAP3K2 | ENSG00000169967.17 | transcript | ENST00000682094.1 | protein_coding | 2/16 | chr2 | TogoVar |