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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ABCC1_chr16_15944616_16148053 | 16139611 | C | CAA | intron_variant | MODIFIER | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(28): Show |
a0001a0002a0010others(1): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0003a0001c0001t0012a0001c0002t0003others(9): Show | a0001c0001t0003g0008a0001c0001t0003g0011a0001c0001t0003g0031others(28): Show | 31 | 249 | 0.1245 | 2 | c.448 others(21): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 30/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ABCC2_chr10_99777640_99857594 | 99778420 | T | TTA | upstream_gene_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(41): Show |
a0001a0004a0018 | a0001c0001a0001c0030a0004c0029others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(3): Show | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0221others(39): Show | 44 | 336 | 0.1310 | 2 | c.-44 others(13): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 4219 | chr10 | TogoVar | ||||||
ABCC2_chr10_99777640_99857594 | 99779377 | C | CTT | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(107): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0001c0005others(11): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0003others(15): Show | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0012others(105): Show | 110 | 336 | 0.3274 | 2 | c.-34 others(13): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 3262 | chr10 | TogoVar | ||||||
ABCC2_chr10_99777640_99857594 | 99781071 | G | GTT | upstream_gene_variant | MODIFIER | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(13): Show |
a0001a0023 | a0001c0002a0023c0034 | a0001c0002t0002a0001c0002t0003a0023c0034t0002 | a0001c0002t0002g0032a0001c0002t0002g0035a0001c0002t0002g0037others(13): Show | 16 | 336 | 0.0476 | 2 | c.-17 others(13): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 1568 | chr10 | TogoVar | ||||||
ABCC2_chr10_99777640_99857594 | 99787155 | C | CAA | intron_variant | MODIFIER | HG00323.hp1 HG00735.hp2 HG01070.hp2 others(5): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0038a0002c0003others(3): Show | a0001c0001t0001a0001c0038t0001a0002c0003t0001others(3): Show | a0001c0001t0001g0262a0001c0038t0001g0139a0002c0003t0001g0326others(5): Show | 8 | 336 | 0.0238 | 2 | c.207 others(19): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ABCC2_chr10_99777640_99857594 | 99789709 | C | CAA | intron_variant | MODIFIER | HG02818.hp1 HG02886.hp2 HG03486.hp1 others(8): Show |
a0001a0026 | a0001c0001a0001c0002a0001c0014others(1): Show | a0001c0001t0001a0001c0002t0007a0001c0014t0001others(1): Show | a0001c0001t0001g0002a0001c0001t0001g0221a0001c0001t0001g0265others(7): Show | 11 | 336 | 0.0327 | 2 | c.208 others(19): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ABCC2_chr10_99777640_99857594 | 99793061 | G | GCA | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
a0001a0002a0003others(24): Show | a0001c0001a0001c0002a0001c0005others(37): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(47): Show | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(325): Show | 333 | 336 | 0.9911 | 2 | c.334 others(17): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ABCC2_chr10_99777640_99857594 | 99814088 | T | TAC | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
a0001a0002a0005others(10): Show | a0001c0001a0001c0030a0002c0003others(12): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(17): Show | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0132others(116): Show | 122 | 336 | 0.3631 | 2 | c.209 others(19): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ABCC2_chr10_99777640_99857594 | 99814162 | C | CAT | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(117): Show |
a0001a0002a0008others(8): Show | a0001c0001a0001c0030a0002c0003others(10): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(15): Show | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0132others(114): Show | 120 | 336 | 0.3571 | 2 | c.209 others(21): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | TogoVar | ||||||
ABCC2_chr10_99777640_99857594 | 99814176 | C | CAT | intron_variant | MODIFIER | HG01884.hp2 HG03130.hp2 NA18522.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0159 | 3 | 336 | 0.0089 | 2 | c.209 others(21): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ABCC2_chr10_99777640_99857594 | 99814256 | T | TAC | intron_variant | MODIFIER | HG01109.hp1 HG01884.hp2 HG03490.hp2 others(2): Show |
a0001a0006 | a0001c0001a0006c0009 | a0001c0001t0001a0006c0009t0001 | a0001c0001t0001g0157a0001c0001t0001g0159a0001c0001t0001g0172others(2): Show | 5 | 336 | 0.0149 | 2 | c.209 others(21): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ABCC2_chr10_99777640_99857594 | 99814270 | T | TAC | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(55): Show |
a0001a0002a0003others(6): Show | a0001c0001a0002c0003a0002c0021others(7): Show | a0001c0001t0001a0002c0003t0001a0002c0003t0004others(9): Show | a0001c0001t0001g0142a0001c0001t0001g0146a0001c0001t0001g0147others(54): Show | 58 | 336 | 0.1726 | 2 | c.209 others(21): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ABCC2_chr10_99777640_99857594 | 99814276 | C | CAT | intron_variant | MODIFIER | HG01167.hp1 HG01169.hp2 HG02818.hp1 others(5): Show |
a0001a0026 | a0001c0002a0001c0014a0026c0032 | a0001c0002t0003a0001c0002t0007a0001c0014t0001others(1): Show | a0001c0002t0003g0130a0001c0002t0003g0131a0001c0002t0003g0224others(5): Show | 8 | 336 | 0.0238 | 2 | c.209 others(21): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | TogoVar | ||||||
ABCC2_chr10_99777640_99857594 | 99814309 | G | GTA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
a0001a0002a0003others(20): Show | a0001c0001a0001c0002a0001c0005others(29): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(35): Show | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(209): Show | 217 | 336 | 0.6458 | 2 | c.209 others(21): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ABCC2_chr10_99777640_99857594 | 99814507 | G | GTA | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(57): Show |
a0001a0008a0018others(1): Show | a0001c0001a0001c0030a0008c0011others(2): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0010others(4): Show | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0132others(55): Show | 60 | 336 | 0.1786 | 2 | c.209 others(21): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ABCC2_chr10_99777640_99857594 | 99814602 | C | CAT | intron_variant | MODIFIER | HG00639.hp2 HG02451.hp2 HG03471.hp1 |
a0001a0019a0020 | a0001c0001a0019c0023a0020c0024 | a0001c0001t0001a0019c0023t0001a0020c0024t0001 | a0001c0001t0001g0114a0019c0023t0001g0219a0020c0024t0001g0013 | 3 | 336 | 0.0089 | 2 | c.209 others(21): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ABCC2_chr10_99777640_99857594 | 99814622 | T | TAC | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(153): Show |
a0001a0002a0003others(13): Show | a0001c0001a0001c0002a0001c0005others(19): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(24): Show | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0137others(150): Show | 156 | 336 | 0.4643 | 2 | c.209 others(21): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ABCC2_chr10_99777640_99857594 | 99814628 | C | CAT | intron_variant | MODIFIER | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(40): Show |
a0001a0004a0008others(3): Show | a0001c0001a0004c0029a0008c0011others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(6): Show | a0001c0001t0001g0004a0001c0001t0001g0132a0001c0001t0001g0133others(39): Show | 43 | 336 | 0.1280 | 2 | c.209 others(21): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ABCC2_chr10_99777640_99857594 | 99814795 | A | ATG | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(129): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0002a0001c0005others(16): Show | a0001c0001t0001a0001c0002t0003a0001c0005t0001others(18): Show | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0137others(126): Show | 132 | 336 | 0.3929 | 2 | c.209 others(21): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ABCC2_chr10_99777640_99857594 | 99815502 | G | GAT | intron_variant | MODIFIER | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(2): Show |
a0005a0007 | a0005c0008a0007c0010 | a0005c0008t0001a0007c0010t0001 | a0005c0008t0001g0028a0005c0008t0001g0045a0005c0008t0001g0075others(2): Show | 5 | 336 | 0.0149 | 2 | c.209 others(21): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | TogoVar | ||||||
ABCC2_chr10_99777640_99857594 | 99837137 | C | CTT | intron_variant | MODIFIER | HG00423.hp1 HG00609.hp2 HG00621.hp2 others(30): Show |
a0001a0002a0016others(2): Show | a0001c0001a0001c0002a0002c0003others(4): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(8): Show | a0001c0001t0001g0114a0001c0001t0001g0147a0001c0001t0001g0271others(30): Show | 33 | 336 | 0.0982 | 2 | c.361 others(19): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 25/31 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
ABCC3_chr17_50629881_50697253 | 50635663 | C | CAG | intron_variant | MODIFIER | HG02886.hp1 HG02976.hp2 HG03098.hp2 others(2): Show |
a0001a0005 | a0001c0001a0001c0002a0005c0008 | a0001c0001t0001a0001c0002t0001a0005c0008t0001 | a0001c0001t0001g0031a0001c0002t0001g0032a0005c0008t0001g0028others(2): Show | 5 | 342 | 0.0146 | 2 | c.45+ others(15): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ABCC3_chr17_50629881_50697253 | 50644310 | C | CAA | intron_variant | MODIFIER | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(17): Show | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0024others(81): Show | 84 | 342 | 0.2456 | 2 | c.45+ others(17): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ABCC3_chr17_50629881_50697253 | 50645371 | C | CAA | intron_variant | MODIFIER | HG01361.hp2 HG02040.hp2 HG02109.hp1 others(7): Show |
a0001a0002a0007 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(3): Show | a0001c0001t0001g0043a0001c0002t0001g0032a0001c0002t0001g0294others(7): Show | 10 | 342 | 0.0292 | 2 | c.45+ others(19): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ABCC3_chr17_50629881_50697253 | 50653758 | G | GAA | intron_variant | MODIFIER | HG01192.hp1 HG02148.hp1 HG02717.hp1 others(3): Show |
a0001a0003a0013 | a0001c0001a0003c0005a0013c0034 | a0001c0001t0001a0003c0005t0002a0013c0034t0001 | a0001c0001t0001g0084a0001c0001t0001g0305a0001c0001t0001g0306others(3): Show | 6 | 342 | 0.0175 | 2 | c.46- others(17): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ABCC3_chr17_50629881_50697253 | 50655404 | C | CAA | intron_variant | MODIFIER | HG00639.hp2 HG00733.hp2 HG01106.hp2 others(12): Show |
a0001a0003a0018 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0002t0001a0001c0003t0001others(4): Show | a0001c0001t0001g0072a0001c0001t0001g0077a0001c0001t0001g0108others(12): Show | 15 | 342 | 0.0439 | 2 | c.46- others(15): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ABCC3_chr17_50629881_50697253 | 50662637 | C | CAA | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(66): Show |
a0001a0002a0004others(7): Show | a0001c0001a0001c0002a0001c0004others(13): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(16): Show | a0001c0001t0001g0014a0001c0001t0001g0031a0001c0001t0001g0041others(66): Show | 69 | 342 | 0.2018 | 2 | c.999 others(19): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 8/30 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ABCC3_chr17_50629881_50697253 | 50671702 | C | CTT | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(56): Show |
a0001a0007a0017others(2): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(11): Show | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0019others(56): Show | 59 | 342 | 0.1725 | 2 | c.224 others(21): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 17/30 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ABCC3_chr17_50629881_50697253 | 50673980 | C | CTT | intron_variant | MODIFIER | HG00438.hp2 HG00738.hp1 HG02080.hp1 others(5): Show |
a0001a0018 | a0001c0001a0001c0002a0018c0031 | a0001c0001t0001a0001c0002t0001a0018c0031t0005 | a0001c0001t0001g0014a0001c0001t0001g0068a0001c0001t0001g0149others(5): Show | 8 | 342 | 0.0234 | 2 | c.259 others(19): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ABCC3_chr17_50629881_50697253 | 50673982 | C | CCT | intron_variant | MODIFIER | HG00099.hp2 HG02622.hp1 HG02622.hp2 others(6): Show |
a0001a0008 | a0001c0001a0001c0017a0008c0016 | a0001c0001t0001a0001c0001t0002a0001c0017t0001others(1): Show | a0001c0001t0001g0034a0001c0001t0001g0120a0001c0001t0001g0136others(6): Show | 9 | 342 | 0.0263 | 2 | c.259 others(19): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | chr17 | TogoVar | ||||||
ABCC3_chr17_50629881_50697253 | 50674798 | A | ATT | intron_variant | MODIFIER | HG00408.hp2 HG00738.hp2 HG02080.hp1 others(15): Show |
a0001a0005a0009 | a0001c0001a0001c0004a0005c0008others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0004t0001others(2): Show | a0001c0001t0001g0014a0001c0001t0001g0036a0001c0001t0001g0048others(15): Show | 18 | 342 | 0.0526 | 2 | c.260 others(19): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 19/30 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ABCC3_chr17_50629881_50697253 | 50696756 | C | CAA | downstream_gene_variant | MODIFIER | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(55): Show |
a0001a0002a0004others(6): Show | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0006others(15): Show | a0001c0001t0001g0114a0001c0001t0001g0136a0001c0001t0001g0137others(55): Show | 58 | 342 | 0.1696 | 2 | c.*55 others(13): Show |
ABCC3 | ENSG00000108846.16 | transcript | ENST00000285238.13 | protein_coding | 4504 | chr17 | TogoVar | ||||||
ABCC4_chr13_95014835_95306451 | 95016387 | C | CTT | downstream_gene_variant | MODIFIER | HG00642.hp1 HG00738.hp2 HG01099.hp2 others(6): Show |
a0001a0002 | a0001c0010a0001c0014a0001c0022others(2): Show | a0001c0010t0007a0001c0014t0007a0001c0022t0022others(2): Show | a0001c0010t0007g0143a0001c0010t0007g0167a0001c0010t0007g0180others(6): Show | 9 | 248 | 0.0363 | 2 | c.*51 others(13): Show |
ABCC4 | ENSG00000125257.16 | transcript | ENST00000645237.2 | protein_coding | 3447 | chr13 | TogoVar | ||||||
ABCC4_chr13_95014835_95306451 | 95017022 | C | CAA | downstream_gene_variant | MODIFIER | HG01243.hp1 HG01243.hp2 HG01975.hp2 others(5): Show |
a0001a0002a0007others(1): Show | a0001c0003a0001c0009a0001c0010others(5): Show | a0001c0003t0001a0001c0009t0023a0001c0010t0024others(5): Show | a0001c0003t0001g0020a0001c0009t0023g0034a0001c0010t0024g0024others(5): Show | 8 | 248 | 0.0323 | 2 | c.*45 others(13): Show |
ABCC4 | ENSG00000125257.16 | transcript | ENST00000645237.2 | protein_coding | 2812 | chr13 | TogoVar | ||||||
ABCC4_chr13_95014835_95306451 | 95024209 | A | AAC | intron_variant | MODIFIER | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(21): Show |
a0001a0002a0007 | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0005others(13): Show | a0001c0001t0001g0173a0001c0001t0005g0044a0001c0002t0005g0027others(21): Show | 24 | 248 | 0.0968 | 2 | c.387 others(21): Show |
ABCC4 | ENSG00000125257.16 | transcript | ENST00000645237.2 | protein_coding | 30/30 | chr13 | TogoVar | ||||||
ABCC4_chr13_95014835_95306451 | 95025393 | C | CCA | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(89): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0002a0001c0003others(31): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0001others(40): Show | a0001c0001t0001g0046a0001c0001t0001g0063a0001c0001t0001g0064others(89): Show | 92 | 248 | 0.3710 | 2 | c.387 others(21): Show |
ABCC4 | ENSG00000125257.16 | transcript | ENST00000645237.2 | protein_coding | 30/30 | chr13 | TogoVar | ||||||
ABCC4_chr13_95014835_95306451 | 95037084 | C | CAA | intron_variant | MODIFIER | HG00642.hp2 HG01169.hp2 HG02148.hp2 others(3): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0005others(2): Show | a0001c0001t0001g0083a0001c0001t0001g0171a0001c0001t0002g0160others(3): Show | 6 | 248 | 0.0242 | 2 | c.373 others(21): Show |
ABCC4 | ENSG00000125257.16 | transcript | ENST00000645237.2 | protein_coding | 29/30 | chr13 | TogoVar | ||||||
ABCC4_chr13_95014835_95306451 | 95038374 | C | CAA | intron_variant | MODIFIER | HG00558.hp1 HG00609.hp2 HG00642.hp1 others(59): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0003others(28): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(41): Show | a0001c0001t0001g0084a0001c0001t0001g0154a0001c0001t0001g0206others(59): Show | 62 | 248 | 0.2500 | 2 | c.373 others(21): Show |
ABCC4 | ENSG00000125257.16 | transcript | ENST00000645237.2 | protein_coding | 29/30 | chr13 | TogoVar | ||||||
ABCC4_chr13_95014835_95306451 | 95047476 | C | CTT | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0002a0001c0003others(39): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(63): Show | a0001c0001t0001g0046a0001c0001t0001g0083a0001c0001t0001g0103others(122): Show | 125 | 248 | 0.5040 | 2 | c.345 others(21): Show |
ABCC4 | ENSG00000125257.16 | transcript | ENST00000645237.2 | protein_coding | 27/30 | chr13 | TogoVar | ||||||
ABCC4_chr13_95014835_95306451 | 95053977 | C | CAA | intron_variant | MODIFIER | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(35): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0009others(17): Show | a0001c0001t0001a0001c0001t0006a0001c0003t0001others(23): Show | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0169others(35): Show | 38 | 248 | 0.1532 | 2 | c.336 others(19): Show |
ABCC4 | ENSG00000125257.16 | transcript | ENST00000645237.2 | protein_coding | 26/30 | chr13 | TogoVar | ||||||
ABCC4_chr13_95014835_95306451 | 95054021 | C | CTT | intron_variant | MODIFIER | HG02145.hp1 HG02647.hp2 HG03017.hp2 others(6): Show |
a0001a0002a0005others(1): Show | a0001c0007a0001c0025a0001c0041others(3): Show | a0001c0007t0002a0001c0025t0009a0001c0041t0009others(4): Show | a0001c0007t0002g0107a0001c0025t0009g0121a0001c0041t0009g0127others(6): Show | 9 | 248 | 0.0363 | 2 | c.336 others(19): Show |
ABCC4 | ENSG00000125257.16 | transcript | ENST00000645237.2 | protein_coding | 26/30 | chr13 | TogoVar | ||||||
ABCC4_chr13_95014835_95306451 | 95058588 | A | AAG | intron_variant | MODIFIER | HG01891.hp2 HG02083.hp1 HG02523.hp2 others(5): Show |
a0001a0002 | a0001c0001a0001c0009a0001c0045others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0009t0005others(4): Show | a0001c0001t0001g0211a0001c0001t0002g0201a0001c0001t0002g0209others(5): Show | 8 | 248 | 0.0323 | 2 | c.336 others(21): Show |
ABCC4 | ENSG00000125257.16 | transcript | ENST00000645237.2 | protein_coding | 26/30 | chr13 | TogoVar | ||||||
ABCC4_chr13_95014835_95306451 | 95061594 | T | TTG | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG01099.hp2 others(19): Show |
a0001a0002a0003others(3): Show | a0001c0002a0001c0003a0001c0007others(9): Show | a0001c0002t0001a0001c0003t0001a0001c0007t0001others(13): Show | a0001c0002t0001g0177a0001c0003t0001g0020a0001c0003t0001g0216others(19): Show | 22 | 248 | 0.0887 | 2 | c.336 others(21): Show |
ABCC4 | ENSG00000125257.16 | transcript | ENST00000645237.2 | protein_coding | 26/30 | chr13 | TogoVar | ||||||
ABCC4_chr13_95014835_95306451 | 95062486 | T | TCA | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(31): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(16): Show | a0001c0001t0001g0154a0001c0001t0001g0173a0001c0001t0001g0198others(31): Show | 34 | 248 | 0.1371 | 2 | c.336 others(19): Show |
ABCC4 | ENSG00000125257.16 | transcript | ENST00000645237.2 | protein_coding | 26/30 | chr13 | TogoVar | ||||||
ABCC4_chr13_95014835_95306451 | 95064260 | G | GTA | intron_variant | MODIFIER | HG00323.hp2 HG00438.hp1 HG02155.hp2 others(7): Show |
a0001a0002 | a0001c0007a0001c0011a0001c0017others(3): Show | a0001c0007t0001a0001c0011t0008a0001c0017t0002others(3): Show | a0001c0007t0001g0237a0001c0011t0008g0244a0001c0017t0002g0086others(7): Show | 10 | 248 | 0.0403 | 2 | c.321 others(21): Show |
ABCC4 | ENSG00000125257.16 | transcript | ENST00000645237.2 | protein_coding | 25/30 | chr13 | TogoVar | ||||||
ABCC4_chr13_95014835_95306451 | 95064486 | T | TAC | intron_variant | MODIFIER | HG01981.hp1 HG02622.hp2 HG03579.hp1 others(1): Show |
a0001a0002 | a0001c0040a0001c0054a0001c0066others(1): Show | a0001c0040t0003a0001c0054t0003a0001c0066t0003others(1): Show | a0001c0040t0003g0124a0001c0054t0003g0131a0001c0066t0003g0035others(1): Show | 4 | 248 | 0.0161 | 2 | c.321 others(21): Show |
ABCC4 | ENSG00000125257.16 | transcript | ENST00000645237.2 | protein_coding | 25/30 | chr13 | TogoVar | ||||||
ABCC4_chr13_95014835_95306451 | 95064498 | C | CAG | intron_variant | MODIFIER | HG02976.hp1 HG03209.hp2 HG03471.hp1 |
a0001 | a0001c0001a0001c0012a0001c0036 | a0001c0001t0006a0001c0012t0006a0001c0036t0001 | a0001c0001t0006g0028a0001c0012t0006g0053a0001c0036t0001g0164 | 3 | 248 | 0.0121 | 2 | c.321 others(21): Show |
ABCC4 | ENSG00000125257.16 | transcript | ENST00000645237.2 | protein_coding | 25/30 | chr13 | TogoVar | ||||||
ABCC4_chr13_95014835_95306451 | 95064513 | A | ATG | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(31): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(18): Show | a0001c0001t0001g0154a0001c0001t0001g0173a0001c0001t0001g0198others(31): Show | 34 | 248 | 0.1371 | 2 | c.321 others(21): Show |
ABCC4 | ENSG00000125257.16 | transcript | ENST00000645237.2 | protein_coding | 25/30 | chr13 | TogoVar | ||||||
ABCC4_chr13_95014835_95306451 | 95071080 | A | ACT | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0002a0001c0003others(47): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(86): Show | a0001c0001t0001g0046a0001c0001t0001g0063a0001c0001t0001g0064others(187): Show | 190 | 248 | 0.7661 | 2 | c.321 others(19): Show |
ABCC4 | ENSG00000125257.16 | transcript | ENST00000645237.2 | protein_coding | 25/30 | chr13 | TogoVar | ||||||
ABCC4_chr13_95014835_95306451 | 95083530 | C | CTT | intron_variant | MODIFIER | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(4): Show |
a0001a0002 | a0001c0013a0001c0024a0002c0015others(1): Show | a0001c0013t0001a0001c0013t0004a0001c0013t0006others(3): Show | a0001c0013t0001g0037a0001c0013t0004g0012a0001c0013t0004g0042others(4): Show | 7 | 248 | 0.0282 | 2 | c.253 others(19): Show |
ABCC4 | ENSG00000125257.16 | transcript | ENST00000645237.2 | protein_coding | 20/30 | chr13 | TogoVar |