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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ME2_chr18_50874118_50959257 | 50941353 | C | CTTTTTTT others(8): Show |
intron_variant | MODIFIER | HG02572.hp2 NA18522.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0181a0002c0002t0042 | a0001c0001t0181g0197 a0002c0002t0042g0316 |
2 | 342 | 0.0059 | 15 | c.158 others(32): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ME2_chr18_50874118_50959257 | 50959102 | C | CTTTCCTT others(8): Show |
downstream_gene_variant | MODIFIER | NA19089.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0287 | 1 | 342 | 0.0029 | 15 | c.*11 others(28): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4846 | chr18 | TogoVar | |||||||
ME2_chr18_50874118_50959257 | 50959188 | T | TCCCTCCC others(8): Show |
downstream_gene_variant | MODIFIER | HG02056.hp1 NA19067.hp1 |
a0001 | a0001c0001 | a0001c0001t0027a0001c0001t0031 | a0001c0001t0027g0047 a0001c0001t0031g0094 |
2 | 342 | 0.0059 | 15 | c.*12 others(28): Show |
ME2 | ENSG00000082212.13 | transcript | ENST00000321341.11 | protein_coding | 4932 | chr18 | TogoVar | |||||||
ME3_chr11_86436108_86677616 | 86468348 | A | ATCCATCC others(8): Show |
intron_variant | MODIFIER | HG01934.hp1 | a0001 | a0001c0009 | a0001c0009t0001 | a0001c0009t0001g0204 | 1 | 320 | 0.0031 | 15 | c.810 others(32): Show |
ME3 | ENSG00000151376.19 | transcript | ENST00000543262.6 | protein_coding | 7/14 | chr11 | TogoVar | |||||||
ME3_chr11_86436108_86677616 | 86501175 | T | TATAATAA others(8): Show |
intron_variant | MODIFIER | HG02735.hp2 HG03490.hp1 HG04115.hp1 others(4): Show |
a0001a0002 | a0001c0002a0001c0010a0002c0008 | a0001c0002t0001a0001c0010t0001a0001c0010t0006others(1): Show | a0001c0002t0001g0032 a0001c0002t0001g0033 a0001c0010t0001g0083 others(4): Show |
7 | 320 | 0.0219 | 15 | c.544 others(32): Show |
ME3 | ENSG00000151376.19 | transcript | ENST00000543262.6 | protein_coding | 5/14 | chr11 | TogoVar | |||||||
ME3_chr11_86436108_86677616 | 86521425 | A | AAAAAATA others(8): Show |
intron_variant | MODIFIER | HG00323.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0142 | 1 | 320 | 0.0031 | 15 | c.468 others(34): Show |
ME3 | ENSG00000151376.19 | transcript | ENST00000543262.6 | protein_coding | 4/14 | chr11 | TogoVar | |||||||
MEAK7_chr16_84471355_84509659 | 84490653 | G | GTGTGTGT others(8): Show |
intron_variant | MODIFIER | NA19010.hp1 | a0001 | a0001c0005 | a0001c0005t0003 | a0001c0005t0003g0361 | 1 | 468 | 0.0021 | 15 | c.385 others(32): Show |
MEAK7 | ENSG00000140950.16 | transcript | ENST00000343629.11 | protein_coding | 3/7 | chr16 | TogoVar | |||||||
MECOM_chr3_169078507_169668712 | 169097817 | T | TAAAAAAA others(8): Show |
intron_variant | MODIFIER | HG00408.hp1 HG01516.hp1 HG02015.hp2 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0010a0001c0001t0013a0001c0001t0016others(3): Show | a0001c0001t0010g0080 a0001c0001t0013g0050 a0001c0001t0016g0064 others(4): Show |
7 | 160 | 0.0438 | 15 | c.285 others(34): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 12/16 | chr3 | TogoVar | |||||||
MECOM_chr3_169078507_169668712 | 169097817 | T | TATAAAAA others(8): Show |
intron_variant | MODIFIER | HG03492.hp2 HG03834.hp1 |
a0001 | a0001c0007 | a0001c0007t0001a0001c0007t0012 | a0001c0007t0001g0054 a0001c0007t0012g0030 |
2 | 160 | 0.0125 | 15 | c.285 others(34): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 12/16 | chr3 | TogoVar | |||||||
MECOM_chr3_169078507_169668712 | 169097817 | T | TTAAAAAA others(8): Show |
intron_variant | MODIFIER | HG04204.hp1 | a0001 | a0001c0001 | a0001c0001t0031 | a0001c0001t0031g0015 | 1 | 160 | 0.0063 | 15 | c.285 others(34): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 12/16 | chr3 | TogoVar | |||||||
MECOM_chr3_169078507_169668712 | 169191718 | A | AAAGAAAG others(8): Show |
intron_variant | MODIFIER | NA18966.hp2 | a0002 | a0002c0011 | a0002c0011t0011 | a0002c0011t0011g0021 | 1 | 160 | 0.0063 | 15 | c.376 others(34): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 2/16 | chr3 | TogoVar | |||||||
MECOM_chr3_169078507_169668712 | 169382879 | A | AAAAAAAA others(8): Show |
intron_variant | MODIFIER | HG02132.hp1 HG02922.hp1 HG03831.hp1 others(3): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(3): Show | a0001c0001t0002g0092 a0001c0001t0004g0063 a0001c0001t0007g0127 others(3): Show |
6 | 160 | 0.0375 | 15 | c.38- others(30): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 1/16 | chr3 | TogoVar | |||||||
MECOM_chr3_169078507_169668712 | 169433686 | A | AAAGAAAG others(8): Show |
intron_variant | MODIFIER | HG00438.hp2 HG00544.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0052 a0001c0001t0002g0076 |
2 | 160 | 0.0125 | 15 | c.38- others(32): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 1/16 | chr3 | TogoVar | |||||||
MECOM_chr3_169078507_169668712 | 169472464 | G | GAAGGAAA others(8): Show |
intron_variant | MODIFIER | HG03516.hp1 NA18941.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0017 | a0001c0001t0002g0084 a0001c0001t0017g0112 |
2 | 160 | 0.0125 | 15 | c.38- others(32): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 1/16 | chr3 | TogoVar | |||||||
MECOM_chr3_169078507_169668712 | 169472518 | G | GAAAGGAA others(8): Show |
intron_variant | MODIFIER | HG01496.hp1 HG02132.hp2 NA18962.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0010a0001c0001t0016a0002c0002t0004 | a0001c0001t0010g0077 a0001c0001t0016g0066 a0002c0002t0004g0068 |
3 | 160 | 0.0188 | 15 | c.38- others(32): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 1/16 | chr3 | TogoVar | |||||||
MECOM_chr3_169078507_169668712 | 169482328 | C | CTTTTTTT others(8): Show |
intron_variant | MODIFIER | NA19088.hp2 | a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0098 | 1 | 160 | 0.0063 | 15 | c.38- others(34): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 1/16 | chr3 | TogoVar | |||||||
MECOM_chr3_169078507_169668712 | 169507650 | C | CTTTTTTT others(8): Show |
intron_variant | MODIFIER | HG02257.hp1 HG02717.hp2 HG02965.hp2 |
a0001 | a0001c0001a0001c0009 | a0001c0001t0003a0001c0001t0016a0001c0009t0007 | a0001c0001t0003g0032 a0001c0001t0016g0069 a0001c0009t0007g0132 |
3 | 160 | 0.0188 | 15 | c.38- others(34): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 1/16 | chr3 | TogoVar | |||||||
MECOM_chr3_169078507_169668712 | 169533591 | T | TTTTTTTT others(8): Show |
intron_variant | MODIFIER | HG02257.hp1 HG02486.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0003a0001c0004t0001 | a0001c0001t0003g0032 a0001c0004t0001g0059 |
2 | 160 | 0.0125 | 15 | c.37+ others(34): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 1/16 | chr3 | TogoVar | |||||||
MECOM_chr3_169078507_169668712 | 169594170 | A | AAAAAAAA others(8): Show |
intron_variant | MODIFIER | HG03130.hp1 NA19043.hp1 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0014 | a0001c0001t0004g0073 a0001c0001t0014g0146 |
2 | 160 | 0.0125 | 15 | c.37+ others(32): Show |
MECOM | ENSG00000085276.19 | transcript | ENST00000651503.2 | protein_coding | 1/16 | chr3 | TogoVar | |||||||
MED12L_chr3_151080664_151441653 | 151081299 | C | CTCCCTTC others(8): Show |
upstream_gene_variant | MODIFIER | NA18986.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0106 | 1 | 280 | 0.0036 | 15 | c.-47 others(26): Show |
MED12L | ENSG00000144893.13 | transcript | ENST00000687756.1 | protein_coding | 4364 | chr3 | TogoVar | |||||||
MED12L_chr3_151080664_151441653 | 151081375 | T | TCCCTCCC others(8): Show |
upstream_gene_variant | MODIFIER | HG00673.hp1 HG00741.hp2 HG01167.hp2 others(30): Show |
a0001a0002a0009 | a0001c0001a0001c0002a0001c0004others(9): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(19): Show | a0001c0001t0002g0196 a0001c0001t0002g0230 a0001c0001t0003g0251 others(30): Show |
33 | 280 | 0.1179 | 15 | c.-46 others(26): Show |
MED12L | ENSG00000144893.13 | transcript | ENST00000687756.1 | protein_coding | 4288 | chr3 | TogoVar | |||||||
MED12L_chr3_151080664_151441653 | 151151031 | C | CTTTTTTT others(8): Show |
intron_variant | MODIFIER | HG01257.hp1 HG02280.hp2 HG02717.hp2 others(6): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0005others(4): Show | a0001c0001t0002a0001c0001t0003a0001c0002t0002others(6): Show | a0001c0001t0002g0243 a0001c0001t0003g0210 a0001c0002t0002g0112 others(6): Show |
9 | 280 | 0.0321 | 15 | c.557 others(32): Show |
MED12L | ENSG00000144893.13 | transcript | ENST00000687756.1 | protein_coding | 5/44 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
MED12L_chr3_151080664_151441653 | 151152085 | G | GTTTTTTT others(8): Show |
intron_variant | MODIFIER | HG02809.hp1 | a0001 | a0001c0019 | a0001c0019t0002 | a0001c0019t0002g0024 | 1 | 280 | 0.0036 | 15 | c.557 others(32): Show |
MED12L | ENSG00000144893.13 | transcript | ENST00000687756.1 | protein_coding | 5/44 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
MED12L_chr3_151080664_151441653 | 151261685 | G | GTGTTTTG others(8): Show |
intron_variant | MODIFIER | HG02486.hp2 HG03098.hp2 HG03453.hp1 others(2): Show |
a0001a0006 | a0001c0001a0001c0007a0001c0018others(2): Show | a0001c0001t0009a0001c0007t0007a0001c0018t0009others(2): Show | a0001c0001t0009g0081 a0001c0007t0007g0033 a0001c0018t0009g0028 others(2): Show |
5 | 280 | 0.0179 | 15 | c.225 others(36): Show |
MED12L | ENSG00000144893.13 | transcript | ENST00000687756.1 | protein_coding | 16/44 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
MED12L_chr3_151080664_151441653 | 151269441 | A | ACACACAC others(8): Show |
intron_variant | MODIFIER | HG03209.hp1 NA18906.hp1 |
a0001 | a0001c0007 | a0001c0007t0007 | a0001c0007t0007g0034 a0001c0007t0007g0036 |
2 | 280 | 0.0071 | 15 | c.225 others(36): Show |
MED12L | ENSG00000144893.13 | transcript | ENST00000687756.1 | protein_coding | 16/44 | chr3 | TogoVar | |||||||
MED12L_chr3_151080664_151441653 | 151270242 | T | TGTGTGTG others(8): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0111 | 1 | 280 | 0.0036 | 15 | c.225 others(36): Show |
MED12L | ENSG00000144893.13 | transcript | ENST00000687756.1 | protein_coding | 16/44 | chr3 | TogoVar | |||||||
MED12L_chr3_151080664_151441653 | 151299356 | C | CTTTCTTT others(8): Show |
intron_variant | MODIFIER | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(45): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | a0001c0001t0001g0213 a0001c0001t0002g0052 a0001c0001t0002g0241 others(45): Show |
48 | 280 | 0.1714 | 15 | c.225 others(36): Show |
MED12L | ENSG00000144893.13 | transcript | ENST00000687756.1 | protein_coding | 16/44 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
MED12L_chr3_151080664_151441653 | 151299398 | T | TTCTTTTC others(8): Show |
intron_variant | MODIFIER | NA18986.hp1 NA19010.hp2 NA19063.hp1 |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0049 | a0001c0002t0001g0106 a0001c0002t0001g0166 a0001c0002t0049g0123 |
3 | 280 | 0.0107 | 15 | c.225 others(36): Show |
MED12L | ENSG00000144893.13 | transcript | ENST00000687756.1 | protein_coding | 16/44 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
MED12L_chr3_151080664_151441653 | 151317436 | C | CTTTTTTT others(8): Show |
intron_variant | MODIFIER | HG02886.hp1 | a0001 | a0001c0002 | a0001c0002t0027 | a0001c0002t0027g0178 | 1 | 280 | 0.0036 | 15 | c.225 others(36): Show |
MED12L | ENSG00000144893.13 | transcript | ENST00000687756.1 | protein_coding | 16/44 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
MED12L_chr3_151080664_151441653 | 151334192 | C | CTTTTTTT others(8): Show |
intron_variant | MODIFIER | HG02080.hp2 | a0001 | a0001c0026 | a0001c0026t0001 | a0001c0026t0001g0045 | 1 | 280 | 0.0036 | 15 | c.225 others(36): Show |
MED12L | ENSG00000144893.13 | transcript | ENST00000687756.1 | protein_coding | 16/44 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
MED12L_chr3_151080664_151441653 | 151368629 | T | TATTTCAT others(8): Show |
intron_variant | MODIFIER | HG01123.hp2 HG02083.hp1 HG03831.hp2 |
a0001 | a0001c0005a0001c0011 | a0001c0005t0001a0001c0011t0002 | a0001c0005t0001g0167 a0001c0005t0001g0187 a0001c0011t0002g0020 |
3 | 280 | 0.0107 | 15 | c.355 others(32): Show |
MED12L | ENSG00000144893.13 | transcript | ENST00000687756.1 | protein_coding | 25/44 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
MED12_chrX_71113596_71147450 | 71132767 | C | CCTCTTCT others(8): Show |
intron_variant | MODIFIER | HG00423.hp1 HG01109.hp1 HG03195.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0024 a0001c0001t0001g0063 a0001c0001t0001g0088 others(3): Show |
7 | 273 | 0.0256 | 15 | c.441 others(30): Show |
MED12 | ENSG00000184634.17 | transcript | ENST00000374080.8 | protein_coding | 31/44 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
MED13L_chr12_115953576_116282693 | 116024773 | C | CGGGGGGG others(8): Show |
intron_variant | MODIFIER | NA18990.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0108 | 1 | 254 | 0.0039 | 15 | c.480 others(32): Show |
MED13L | ENSG00000123066.9 | transcript | ENST00000281928.9 | protein_coding | 4/30 | chr12 | TogoVar | |||||||
MED13L_chr12_115953576_116282693 | 116031756 | A | AAAGAAGG others(8): Show |
intron_variant | MODIFIER | HG06807.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0180 | 1 | 254 | 0.0039 | 15 | c.480 others(32): Show |
MED13L | ENSG00000123066.9 | transcript | ENST00000281928.9 | protein_coding | 4/30 | chr12 | TogoVar | |||||||
MED13L_chr12_115953576_116282693 | 116031756 | A | AAGGAAGG others(8): Show |
intron_variant | MODIFIER | HG00140.hp1 NA18612.hp1 NA18946.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0104 a0001c0001t0001g0141 a0001c0001t0001g0214 others(1): Show |
4 | 254 | 0.0158 | 15 | c.480 others(32): Show |
MED13L | ENSG00000123066.9 | transcript | ENST00000281928.9 | protein_coding | 4/30 | chr12 | TogoVar | |||||||
MED13L_chr12_115953576_116282693 | 116096354 | C | CAAAAAAA others(8): Show |
intron_variant | MODIFIER | HG00323.hp1 HG01517.hp2 NA18963.hp1 others(3): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0041 a0001c0001t0001g0161 a0001c0001t0001g0214 others(3): Show |
6 | 254 | 0.0236 | 15 | c.479 others(30): Show |
MED13L | ENSG00000123066.9 | transcript | ENST00000281928.9 | protein_coding | 4/30 | chr12 | TogoVar | |||||||
MED13L_chr12_115953576_116282693 | 116148051 | C | CAAAAAAA others(8): Show |
intron_variant | MODIFIER | HG03209.hp2 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0098 | 1 | 254 | 0.0039 | 15 | c.311 others(34): Show |
MED13L | ENSG00000123066.9 | transcript | ENST00000281928.9 | protein_coding | 2/30 | chr12 | TogoVar | |||||||
MED13L_chr12_115953576_116282693 | 116185652 | G | GCTTTTCT others(8): Show |
intron_variant | MODIFIER | HG02486.hp1 HG02895.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0101 a0001c0001t0003g0003 |
2 | 254 | 0.0079 | 15 | c.310 others(34): Show |
MED13L | ENSG00000123066.9 | transcript | ENST00000281928.9 | protein_coding | 2/30 | chr12 | TogoVar | |||||||
MED13_chr17_61937605_62070278 | 62015954 | A | ATATATAT others(8): Show |
intron_variant | MODIFIER | NA18946.hp1 | a0001 | a0001c0002 | a0001c0002t0026 | a0001c0002t0026g0034 | 1 | 326 | 0.0031 | 15 | c.128 others(34): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 8/29 | chr17 | TogoVar | |||||||
MED13_chr17_61937605_62070278 | 62049078 | C | CAAAAAAA others(8): Show |
intron_variant | MODIFIER | HG02559.hp2 HG02896.hp2 HG02970.hp2 others(2): Show |
a0001 | a0001c0002a0001c0003a0001c0009 | a0001c0002t0001a0001c0003t0001a0001c0009t0001 | a0001c0002t0001g0053 a0001c0003t0001g0109 a0001c0003t0001g0110 others(2): Show |
5 | 326 | 0.0153 | 15 | c.470 others(32): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | TogoVar | |||||||
MED13_chr17_61937605_62070278 | 62049930 | C | CAAAAAAA others(8): Show |
intron_variant | MODIFIER | HG02630.hp2 | a0001 | a0001c0017 | a0001c0017t0001 | a0001c0017t0001g0322 | 1 | 326 | 0.0031 | 15 | c.470 others(32): Show |
MED13 | ENSG00000108510.10 | transcript | ENST00000397786.7 | protein_coding | 3/29 | chr17 | TogoVar | |||||||
MED15_chr22_20502610_20592619 | 20505559 | C | CAAAAAAA others(8): Show |
upstream_gene_variant | MODIFIER | HG01106.hp2 HG01167.hp2 HG02970.hp2 others(3): Show |
a0001a0007 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0002t0008a0001c0004t0001others(2): Show | a0001c0001t0001g0280 a0001c0001t0001g0285 a0001c0002t0008g0222 others(3): Show |
6 | 341 | 0.0176 | 15 | c.-21 others(26): Show |
MED15 | ENSG00000099917.17 | transcript | ENST00000263205.11 | protein_coding | 2050 | chr22 | TogoVar | |||||||
MED17_chr11_93779282_93819963 | 93793114 | C | CTTTTTTT others(8): Show |
intron_variant | MODIFIER | HG01255.hp1 HG01978.hp1 HG02004.hp2 others(15): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0001t0016a0001c0001t0023others(4): Show | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0069 others(12): Show |
18 | 320 | 0.0563 | 15 | c.638 others(30): Show |
MED17 | ENSG00000042429.12 | transcript | ENST00000251871.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
MED1_chr17_39399285_39456263 | 39440019 | A | AAGGAAGG others(8): Show |
intron_variant | MODIFIER | HG02129.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0250 | 1 | 280 | 0.0036 | 15 | c.399 others(30): Show |
MED1 | ENSG00000125686.12 | transcript | ENST00000300651.11 | protein_coding | 5/16 | chr17 | TogoVar | |||||||
MED20_chr6_41900354_41926139 | 41916258 | T | TAAATAAA others(8): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0162 | 1 | 444 | 0.0023 | 15 | c.169 others(30): Show |
MED20 | ENSG00000124641.16 | transcript | ENST00000265350.9 | protein_coding | 2/3 | chr6 | TogoVar | |||||||
MED21_chr12_27017558_27035673 | 27022149 | C | CAATAAAT others(8): Show |
upstream_gene_variant | MODIFIER | HG02280.hp1 HG02280.hp2 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0004 | 2 | 426 | 0.0047 | 15 | c.-43 others(24): Show |
MED21 | ENSG00000152944.9 | transcript | ENST00000282892.4 | protein_coding | 408 | chr12 | TogoVar | |||||||
MED25_chr19_49813289_49841979 | 49815352 | C | CAAAAAAA others(8): Show |
upstream_gene_variant | MODIFIER | NA18906.hp2 NA18971.hp1 NA18981.hp2 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0007 a0001c0003t0001g0041 a0001c0003t0001g0044 others(3): Show |
7 | 406 | 0.0172 | 15 | c.-29 others(26): Show |
MED25 | ENSG00000104973.19 | transcript | ENST00000312865.10 | protein_coding | 2936 | chr19 | TogoVar | |||||||
MED26_chr19_16569919_16633204 | 16609336 | A | AAAAAAAA others(8): Show |
intron_variant | MODIFIER | HG00099.hp1 HG01175.hp2 HG01496.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0025 a0001c0001t0001g0079 a0001c0001t0001g0080 others(5): Show |
8 | 268 | 0.0299 | 15 | c.72+ others(32): Show |
MED26 | ENSG00000105085.11 | transcript | ENST00000263390.8 | protein_coding | 1/2 | chr19 | TogoVar | |||||||
MED27_chr9_131855112_132084867 | 131966383 | C | CAAAAAAA others(8): Show |
intron_variant | MODIFIER | HG00738.hp1 HG01255.hp2 HG01258.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0086 others(6): Show |
9 | 274 | 0.0329 | 15 | c.480 others(34): Show |
MED27 | ENSG00000160563.14 | transcript | ENST00000292035.10 | protein_coding | 3/7 | chr9 | TogoVar | |||||||
MED28_chr4_17609641_17639105 | 17613882 | T | TAAAAAAA others(8): Show |
upstream_gene_variant | MODIFIER | HG01109.hp1 HG02630.hp2 HG02896.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0009a0001c0001t0032a0001c0001t0033others(1): Show | a0001c0001t0009g0003 a0001c0001t0032g0015 a0001c0001t0033g0015 others(1): Show |
4 | 328 | 0.0122 | 15 | c.-77 others(24): Show |
MED28 | ENSG00000118579.13 | transcript | ENST00000237380.12 | protein_coding | 758 | chr4 | TogoVar |