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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ABCC1_chr16_15944616_16148053 | 15944717 | GTA | G | upstream_gene_variant | MODIFIER | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(12): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(7): Show | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0160 others(12): Show |
15 | 117 | 0.1282 | -2 | c.-50 others(13): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 4898 | chr16 | TogoVar | |||||||
ABCC1_chr16_15944616_16148053 | 15952716 | TAA | T | intron_variant | MODIFIER | HG00280.hp2 HG00597.hp1 HG00639.hp2 others(34): Show |
a0001a0002a0006others(1): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(26): Show | a0001c0001t0001g0037 a0001c0001t0001g0086 a0001c0001t0004g0118 others(34): Show |
37 | 46 | 0.8043 | -2 | c.48+ others(17): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 15961023 | TTA | T | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(35): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(25): Show | a0001c0001t0001g0017 a0001c0001t0001g0037 a0001c0001t0001g0084 others(35): Show |
38 | 248 | 0.1532 | -2 | c.48+ others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 1/30 | chr16 | TogoVar | |||||||
ABCC1_chr16_15944616_16148053 | 15965464 | TTG | T | intron_variant | MODIFIER | HG01884.hp2 HG02257.hp2 HG02622.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0007others(1): Show | a0001c0001t0001a0001c0001t0017a0001c0002t0001others(4): Show | a0001c0001t0001g0017 a0001c0001t0017g0023 a0001c0002t0001g0028 others(4): Show |
7 | 248 | 0.0282 | -2 | c.48+ others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 15967758 | CAA | C | intron_variant | MODIFIER | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(18): Show |
a0001a0010 | a0001c0001a0001c0002a0001c0005others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(10): Show | a0001c0001t0001g0084 a0001c0001t0003g0008 a0001c0001t0004g0106 others(18): Show |
21 | 72 | 0.2917 | -2 | c.48+ others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 15972787 | CTT | C | intron_variant | MODIFIER | HG01109.hp2 HG02630.hp2 HG02895.hp2 others(5): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0005a0001c0001t0006a0001c0001t0010others(2): Show | a0001c0001t0005g0104 a0001c0001t0006g0093 a0001c0001t0006g0096 others(5): Show |
8 | 71 | 0.1127 | -2 | c.48+ others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 15981881 | GCT | G | intron_variant | MODIFIER | HG01884.hp2 HG02257.hp2 HG02622.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0007others(1): Show | a0001c0001t0017a0001c0002t0001a0001c0007t0001others(2): Show | a0001c0001t0017g0023 a0001c0002t0001g0028 a0001c0007t0001g0026 others(2): Show |
5 | 248 | 0.0202 | -2 | c.49- others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 1/30 | chr16 | TogoVar | |||||||
ABCC1_chr16_15944616_16148053 | 15989068 | CAA | C | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(103): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(18): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(48): Show | a0001c0001t0001g0037 a0001c0001t0001g0138 a0001c0001t0001g0160 others(103): Show |
106 | 121 | 0.8760 | -2 | c.49- others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 15990816 | ATT | A | intron_variant | MODIFIER | HG00673.hp1 HG01081.hp1 NA18953.hp1 others(2): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0018a0001c0004t0002 | a0001c0001t0001g0160 a0001c0001t0018g0168 a0001c0004t0002g0158 others(2): Show |
5 | 97 | 0.0515 | -2 | c.49- others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 15999850 | CTT | C | intron_variant | MODIFIER | HG02886.hp2 HG03130.hp2 NA19043.hp1 |
a0001 | a0001c0007a0001c0022 | a0001c0007t0001a0001c0007t0005a0001c0022t0009 | a0001c0007t0001g0026 a0001c0007t0005g0113 a0001c0022t0009g0006 |
3 | 247 | 0.0121 | -2 | c.49- others(17): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16005349 | ATT | A | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(73): Show |
a0001a0004a0005 | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0014a0001c0001t0018others(31): Show | a0001c0001t0001g0071 a0001c0001t0001g0160 a0001c0001t0001g0213 others(73): Show |
76 | 213 | 0.3568 | -2 | c.49- others(17): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16007214 | TTG | T | intron_variant | MODIFIER | HG02257.hp2 HG02572.hp1 HG02735.hp2 others(1): Show |
a0001 | a0001c0001a0001c0003a0001c0007 | a0001c0001t0012a0001c0003t0001a0001c0003t0005others(1): Show | a0001c0001t0012g0044 a0001c0003t0001g0036 a0001c0003t0005g0046 others(1): Show |
4 | 150 | 0.0267 | -2 | c.49- others(15): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 1/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16010037 | CTT | C | intron_variant | MODIFIER | HG00642.hp1 HG01175.hp1 HG02145.hp2 others(4): Show |
a0001a0004 | a0001c0002a0001c0003a0001c0032others(2): Show | a0001c0002t0006a0001c0002t0008a0001c0002t0018others(4): Show | a0001c0002t0006g0108 a0001c0002t0008g0043 a0001c0002t0018g0039 others(4): Show |
7 | 40 | 0.1750 | -2 | c.351 others(17): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 3/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16012700 | TCC | T | intron_variant | MODIFIER | HG00597.hp2 HG00621.hp2 HG00639.hp1 others(35): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(27): Show | a0001c0001t0001g0084 a0001c0001t0003g0008 a0001c0001t0004g0118 others(35): Show |
38 | 248 | 0.1532 | -2 | c.352 others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 3/30 | chr16 | TogoVar | |||||||
ABCC1_chr16_15944616_16148053 | 16016984 | TAA | T | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(130): Show |
a0001a0003a0004others(4): Show | a0001c0001a0001c0002a0001c0003others(23): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(60): Show | a0001c0001t0001g0084 a0001c0001t0003g0008 a0001c0001t0003g0061 others(130): Show |
133 | 248 | 0.5363 | -2 | c.615 others(17): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 5/30 | chr16 | TogoVar | |||||||
ABCC1_chr16_15944616_16148053 | 16017082 | CCT | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(65): Show |
a0001a0004a0008others(1): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(30): Show | a0001c0001t0003g0061 a0001c0001t0004g0106 a0001c0001t0004g0170 others(65): Show |
68 | 248 | 0.2742 | -2 | c.615 others(17): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 5/30 | chr16 | TogoVar | |||||||
ABCC1_chr16_15944616_16148053 | 16022917 | GTT | G | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(60): Show |
a0001a0004a0008others(1): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0003a0001c0001t0004a0001c0001t0006others(28): Show | a0001c0001t0003g0061 a0001c0001t0004g0170 a0001c0001t0004g0240 others(60): Show |
63 | 248 | 0.2540 | -2 | c.615 others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16026465 | CTT | C | intron_variant | MODIFIER | HG02257.hp1 HG02486.hp1 HG02976.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0005a0001c0001t0012 | a0001c0001t0004g0106 a0001c0001t0005g0024 a0001c0001t0005g0025 others(3): Show |
6 | 119 | 0.0504 | -2 | c.616 others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 5/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16034023 | CTT | C | intron_variant | MODIFIER | HG00099.hp2 HG01109.hp2 HG01261.hp2 others(19): Show |
a0001a0007a0010 | a0001c0001a0001c0005a0001c0006others(6): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(14): Show | a0001c0001t0005g0099 a0001c0001t0005g0101 a0001c0001t0006g0093 others(19): Show |
22 | 67 | 0.3284 | -2 | c.677 others(17): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 6/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16039209 | TTG | T | intron_variant | MODIFIER | HG01109.hp2 HG02145.hp1 HG02257.hp1 others(10): Show |
a0001a0003 | a0001c0001a0001c0008a0001c0040others(1): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(5): Show | a0001c0001t0004g0106 a0001c0001t0005g0094 a0001c0001t0005g0104 others(10): Show |
13 | 226 | 0.0575 | -2 | c.809 others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16039233 | GTA | G | intron_variant | MODIFIER | HG02055.hp2 HG02622.hp1 HG02818.hp2 others(7): Show |
a0001a0004a0009 | a0001c0001a0001c0007a0001c0008others(4): Show | a0001c0001t0008a0001c0001t0016a0001c0001t0017others(6): Show | a0001c0001t0008g0002 a0001c0001t0016g0018 a0001c0001t0016g0019 others(7): Show |
10 | 248 | 0.0403 | -2 | c.809 others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16039239 | ATG | A | intron_variant | MODIFIER | HG00408.hp1 HG01109.hp2 HG02109.hp1 others(14): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(9): Show | a0001c0001t0004g0106 a0001c0001t0005g0094 a0001c0001t0005g0104 others(14): Show |
17 | 138 | 0.1232 | -2 | c.809 others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16042173 | GTT | G | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(93): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0005a0001c0006others(18): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(41): Show | a0001c0001t0001g0017 a0001c0001t0001g0031 a0001c0001t0001g0037 others(93): Show |
96 | 206 | 0.4660 | -2 | c.810 others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 7/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16049564 | AAC | A | intron_variant | MODIFIER | HG02257.hp1 HG02486.hp1 HG02486.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0012 | a0001c0001t0005g0094 a0001c0001t0005g0104 a0001c0001t0005g0107 others(1): Show |
4 | 248 | 0.0161 | -2 | c.138 others(21): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 10/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16053774 | CAA | C | intron_variant | MODIFIER | HG00099.hp2 HG00639.hp1 HG01884.hp2 others(12): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(9): Show | a0001c0001t0001g0084 a0001c0001t0004g0170 a0001c0001t0006g0166 others(12): Show |
15 | 47 | 0.3191 | -2 | c.147 others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 11/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16061772 | CTT | C | intron_variant | MODIFIER | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(39): Show |
a0001a0008 | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(19): Show | a0001c0001t0001g0037 a0001c0001t0001g0071 a0001c0001t0001g0083 others(39): Show |
42 | 181 | 0.2320 | -2 | c.167 others(21): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 12/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16074947 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
a0001a0003a0004others(4): Show | a0001c0001a0001c0002a0001c0003others(28): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(61): Show | a0001c0001t0001g0017 a0001c0001t0001g0031 a0001c0001t0001g0037 others(164): Show |
167 | 219 | 0.7626 | -2 | c.191 others(21): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 14/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16087658 | CAT | C | intron_variant | MODIFIER | HG00609.hp1 HG00642.hp1 HG01981.hp1 others(8): Show |
a0001a0002a0006 | a0001c0001a0001c0033a0002c0010others(2): Show | a0001c0001t0008a0001c0033t0015a0002c0010t0002others(3): Show | a0001c0001t0008g0181 a0001c0033t0015g0098 a0002c0010t0002g0076 others(8): Show |
11 | 248 | 0.0444 | -2 | c.246 others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 18/30 | chr16 | TogoVar | |||||||
ABCC1_chr16_15944616_16148053 | 16088124 | CGT | C | intron_variant | MODIFIER | HG00609.hp1 HG00642.hp1 HG01981.hp1 others(11): Show |
a0001a0002a0006 | a0001c0001a0001c0002a0001c0033others(3): Show | a0001c0001t0005a0001c0001t0008a0001c0001t0011others(6): Show | a0001c0001t0005g0094 a0001c0001t0008g0181 a0001c0001t0011g0097 others(11): Show |
14 | 185 | 0.0757 | -2 | c.246 others(21): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 18/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16090365 | CAT | C | intron_variant | MODIFIER | HG00609.hp1 HG00642.hp1 HG01981.hp1 others(8): Show |
a0001a0002a0006 | a0001c0001a0001c0033a0002c0010others(2): Show | a0001c0001t0008a0001c0033t0015a0002c0010t0002others(3): Show | a0001c0001t0008g0181 a0001c0033t0015g0098 a0002c0010t0002g0076 others(8): Show |
11 | 248 | 0.0444 | -2 | c.246 others(17): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 18/30 | chr16 | TogoVar | |||||||
ABCC1_chr16_15944616_16148053 | 16100482 | CAT | C | intron_variant | MODIFIER | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(50): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0004others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(28): Show | a0001c0001t0001g0037 a0001c0001t0001g0071 a0001c0001t0001g0083 others(50): Show |
53 | 248 | 0.2137 | -2 | c.264 others(21): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 19/30 | chr16 | TogoVar | |||||||
ABCC1_chr16_15944616_16148053 | 16106416 | GAA | G | intron_variant | MODIFIER | HG02258.hp1 HG02723.hp1 HG02895.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0007 | a0001c0001t0001a0001c0001t0008a0001c0001t0016others(2): Show | a0001c0001t0001g0017 a0001c0001t0008g0181 a0001c0001t0016g0019 others(2): Show |
5 | 13 | 0.3846 | -2 | c.273 others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 20/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16108273 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(41): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(19): Show | a0001c0001t0001g0068 a0001c0001t0001g0134 a0001c0001t0003g0011 others(41): Show |
44 | 97 | 0.4536 | -2 | c.287 others(21): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 21/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16112374 | CAA | C | intron_variant | MODIFIER | HG01496.hp1 HG01884.hp2 HG02145.hp1 others(3): Show |
a0001a0003 | a0001c0002a0001c0012a0003c0026others(2): Show | a0001c0002t0001a0001c0002t0010a0001c0012t0002others(3): Show | a0001c0002t0001g0028 a0001c0002t0010g0085 a0001c0012t0002g0155 others(3): Show |
6 | 213 | 0.0282 | -2 | c.307 others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 22/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16115377 | CAG | C | intron_variant | MODIFIER | HG01884.hp2 HG03540.hp1 NA19240.hp2 others(1): Show |
a0001 | a0001c0002a0001c0012 | a0001c0002t0001a0001c0002t0002a0001c0002t0010others(1): Show | a0001c0002t0001g0028 a0001c0002t0002g0150 a0001c0002t0010g0085 others(1): Show |
4 | 248 | 0.0161 | -2 | c.339 others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 23/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16118883 | TAA | T | intron_variant | MODIFIER | HG00558.hp1 HG00639.hp1 HG01175.hp1 others(13): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(11): Show | a0001c0001t0001g0138 a0001c0001t0001g0219 a0001c0001t0001g0220 others(13): Show |
16 | 126 | 0.1270 | -2 | c.339 others(21): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 23/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16119843 | AAG | A | intron_variant | MODIFIER | HG02723.hp1 HG02896.hp2 HG02922.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0006a0001c0002t0001 | a0001c0001t0001g0017 a0001c0001t0006g0166 a0001c0001t0006g0171 others(1): Show |
4 | 248 | 0.0161 | -2 | c.339 others(21): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 23/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16122711 | TAA | T | intron_variant | MODIFIER | HG02257.hp1 HG02486.hp1 HG02717.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003a0001c0006 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(4): Show | a0001c0001t0001g0084 a0001c0001t0003g0141 a0001c0001t0005g0107 others(4): Show |
7 | 115 | 0.0609 | -2 | c.359 others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 24/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16124377 | CTG | C | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp2 HG00738.hp2 others(34): Show |
a0001a0005a0008others(1): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(21): Show | a0001c0001t0001g0086 a0001c0001t0001g0125 a0001c0001t0003g0008 others(34): Show |
37 | 226 | 0.1637 | -2 | c.359 others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 24/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16132510 | GTT | G | intron_variant | MODIFIER | HG00639.hp1 HG01261.hp1 HG01517.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0008a0001c0002t0008a0001c0003t0001others(4): Show | a0001c0001t0008g0246 a0001c0002t0008g0162 a0001c0003t0001g0205 others(6): Show |
9 | 121 | 0.0744 | -2 | c.396 others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 27/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16134625 | CTT | C | intron_variant | MODIFIER | HG00642.hp1 HG00738.hp2 HG01496.hp2 others(14): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0006a0001c0001t0008a0001c0001t0017others(12): Show | a0001c0001t0006g0045 a0001c0001t0006g0171 a0001c0001t0008g0057 others(14): Show |
17 | 41 | 0.4146 | -2 | c.412 others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 28/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16136013 | CTT | C | intron_variant | MODIFIER | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(34): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0012others(13): Show | a0001c0001t0001g0031 a0001c0001t0003g0008 a0001c0001t0003g0011 others(34): Show |
37 | 78 | 0.4744 | -2 | c.412 others(19): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 28/30 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | ||||||
ABCC1_chr16_15944616_16148053 | 16147235 | TTG | T | downstream_gene_variant | MODIFIER | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(14): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0005a0001c0002t0005a0001c0003t0005others(2): Show | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0094 others(14): Show |
17 | 248 | 0.0685 | -2 | c.*59 others(13): Show |
ABCC1 | ENSG00000103222.20 | transcript | ENST00000399410.8 | protein_coding | 4183 | chr16 | TogoVar | |||||||
ABCC2_chr10_99777640_99857594 | 99780094 | CTT | C | upstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(85): Show |
a0001a0002a0004others(6): Show | a0001c0001a0001c0002a0001c0014others(10): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(14): Show | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0058 others(85): Show |
88 | 174 | 0.5057 | -2 | c.-27 others(13): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 2545 | chr10 | TogoVar | |||||||
ABCC2_chr10_99777640_99857594 | 99788066 | CAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(213): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0002a0001c0005others(24): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(30): Show | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(206): Show |
216 | 329 | 0.6565 | -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 | 99806077 | CTG | C | intron_variant | MODIFIER | HG01884.hp2 HG02683.hp2 HG02896.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0005a0001c0002t0003 | a0001c0001t0001g0161 a0001c0001t0001g0205 a0001c0001t0001g0206 others(8): Show |
11 | 22 | 0.5000 | -2 | c.153 others(19): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
ABCC2_chr10_99777640_99857594 | 99814177 | ATG | A | intron_variant | MODIFIER | HG02055.hp2 HG03942.hp1 NA18940.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0001a0001c0002t0003a0001c0005t0001 | a0001c0001t0001g0008 a0001c0001t0001g0205 a0001c0001t0001g0206 others(7): Show |
11 | 326 | 0.0337 | -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 | 99814192 | CAT | C | intron_variant | MODIFIER | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(3): Show |
a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0006 a0002c0003t0001g0289 a0002c0003t0001g0311 others(2): Show |
6 | 327 | 0.0183 | -2 | c.209 others(21): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | chr10 | TogoVar | |||||||
ABCC2_chr10_99777640_99857594 | 99814193 | ATG | A | intron_variant | MODIFIER | HG00140.hp2 HG01074.hp1 HG02300.hp2 others(3): Show |
a0001a0005a0006 | a0001c0001a0005c0008a0006c0010 | a0001c0001t0001a0005c0008t0001a0006c0010t0001 | a0001c0001t0001g0118 a0005c0008t0001g0030 a0005c0008t0001g0047 others(3): Show |
6 | 333 | 0.0180 | -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 | 99814211 | ATG | A | intron_variant | MODIFIER | HG00140.hp2 HG01074.hp1 HG02809.hp2 others(1): Show |
a0005a0006 | a0005c0008a0006c0010 | a0005c0008t0001a0006c0010t0001 | a0005c0008t0001g0030 a0005c0008t0001g0047 a0006c0010t0001g0010 others(1): Show |
4 | 332 | 0.0120 | -2 | c.209 others(21): Show |
ABCC2 | ENSG00000023839.12 | transcript | ENST00000647814.1 | protein_coding | 16/31 | INFO_REALIGN_3_PRIME | chr10 | TogoVar |