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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ATP10D_chr4_47480275_47598486 | 47488612 | CAAAA | C | intron_variant | MODIFIER | HG01517.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
a0001a0002a0003others(4): Show | a0001c0003a0001c0031a0002c0002others(5): Show | a0001c0003t0001a0001c0031t0002a0002c0002t0001others(5): Show | a0001c0003t0001g0117a0001c0031t0002g0204a0002c0002t0001g0122others(8): Show | 11 | 332 | 0.0331 | -4 | c.-38 others(21): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ATP10D_chr4_47480275_47598486 | 47509943 | GGTGT | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(128): Show |
a0001a0002a0003others(19): Show | a0001c0001a0001c0003a0001c0016others(25): Show | a0001c0001t0003a0001c0001t0004a0001c0003t0001others(36): Show | a0001c0001t0003g0010a0001c0001t0003g0213a0001c0001t0003g0229others(125): Show | 131 | 332 | 0.3946 | -4 | c.-37 others(21): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ATP10D_chr4_47480275_47598486 | 47514807 | GTTAA | G | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp1 NA18950.hp2 |
a0016 | a0016c0018 | a0016c0018t0010 | a0016c0018t0010g0275a0016c0018t0010g0295a0016c0018t0010g0317 | 3 | 332 | 0.0090 | -4 | c.291 others(19): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ATP10D_chr4_47480275_47598486 | 47528458 | GGTGT | G | intron_variant | MODIFIER | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(57): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0003a0002c0002others(12): Show | a0001c0001t0003a0001c0001t0004a0001c0003t0001others(17): Show | a0001c0001t0003g0010a0001c0001t0003g0213a0001c0001t0003g0238others(56): Show | 60 | 332 | 0.1807 | -4 | c.776 others(21): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ATP10D_chr4_47480275_47598486 | 47530446 | TTTTG | T | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
a0001a0002a0008others(19): Show | a0001c0003a0002c0002a0002c0008others(21): Show | a0001c0003t0001a0002c0002t0001a0002c0002t0002others(28): Show | a0001c0003t0001g0024a0001c0003t0001g0054a0001c0003t0001g0058others(69): Show | 75 | 332 | 0.2259 | -4 | c.776 others(21): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ATP10D_chr4_47480275_47598486 | 47536261 | AAGAG | A | intron_variant | MODIFIER | HG00639.hp1 HG01433.hp1 HG02300.hp2 |
a0001a0002 | a0001c0003a0002c0002 | a0001c0003t0001a0002c0002t0001 | a0001c0003t0001g0034a0002c0002t0001g0031a0002c0002t0001g0032 | 3 | 332 | 0.0090 | -4 | c.101 others(21): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ATP10D_chr4_47480275_47598486 | 47543834 | TGTAC | T | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(83): Show |
a0002a0003a0004others(11): Show | a0002c0002a0003c0004a0004c0005others(13): Show | a0002c0002t0001a0003c0004t0005a0003c0004t0006others(20): Show | a0002c0002t0001g0109a0002c0002t0001g0111a0002c0002t0001g0122others(79): Show | 86 | 332 | 0.2590 | -4 | c.139 others(23): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | chr4 | TogoVar | ||||||
ATP10D_chr4_47480275_47598486 | 47545593 | TAAGA | T | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00438.hp2 others(82): Show |
a0002a0003a0004others(11): Show | a0002c0002a0003c0004a0004c0005others(12): Show | a0002c0002t0001a0003c0004t0005a0003c0004t0006others(19): Show | a0002c0002t0001g0109a0002c0002t0001g0111a0002c0002t0001g0122others(78): Show | 85 | 332 | 0.2560 | -4 | c.139 others(23): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ATP10D_chr4_47480275_47598486 | 47572644 | CGTGT | C | intron_variant | MODIFIER | HG00735.hp1 HG01069.hp2 HG01109.hp2 others(1): Show |
a0002a0004a0014 | a0002c0008a0004c0005a0014c0019 | a0002c0008t0001a0004c0005t0005a0014c0019t0004 | a0002c0008t0001g0198a0004c0005t0005g0140a0014c0019t0004g0029others(1): Show | 4 | 332 | 0.0121 | -4 | c.324 others(21): Show |
ATP10D | ENSG00000145246.14 | transcript | ENST00000273859.8 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112697727 | GTTTT | G | intron_variant | MODIFIER | HG02258.hp2 HG02922.hp1 HG03225.hp1 others(2): Show |
a0001a0004 | a0001c0002a0001c0014a0001c0019others(1): Show | a0001c0002t0015a0001c0002t0032a0001c0014t0003others(2): Show | a0001c0002t0015g0054a0001c0002t0032g0179a0001c0014t0003g0178others(2): Show | 5 | 254 | 0.0197 | -4 | c.39+ others(19): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112740148 | CTATA | C | intron_variant | MODIFIER | HG01106.hp2 HG01934.hp1 HG03130.hp1 others(3): Show |
a0001 | a0001c0001a0001c0004a0001c0005others(2): Show | a0001c0001t0001a0001c0004t0001a0001c0004t0003others(3): Show | a0001c0001t0001g0104a0001c0004t0001g0106a0001c0004t0003g0149others(3): Show | 6 | 254 | 0.0236 | -4 | c.40- others(21): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112755135 | CCAAA | C | intron_variant | MODIFIER | HG01123.hp2 HG01891.hp2 HG02148.hp1 others(2): Show |
a0001a0002 | a0001c0004a0001c0017a0001c0044others(1): Show | a0001c0004t0006a0001c0017t0058a0001c0044t0045others(1): Show | a0001c0004t0006g0058a0001c0004t0006g0061a0001c0017t0058g0053others(2): Show | 5 | 254 | 0.0197 | -4 | c.40- others(21): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112803865 | CCTTG | C | intron_variant | MODIFIER | HG01169.hp1 HG02055.hp2 HG03041.hp2 others(1): Show |
a0001 | a0001c0002a0001c0004a0001c0016 | a0001c0002t0014a0001c0004t0006a0001c0016t0004 | a0001c0002t0014g0213a0001c0004t0006g0203a0001c0016t0004g0214others(1): Show | 4 | 254 | 0.0158 | -4 | c.163 others(21): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112804132 | CCCCA | C | intron_variant | MODIFIER | HG02055.hp2 HG02129.hp1 HG03041.hp2 others(2): Show |
a0001a0002 | a0001c0002a0001c0016a0002c0003others(1): Show | a0001c0002t0014a0001c0016t0004a0002c0003t0002others(1): Show | a0001c0002t0014g0213a0001c0016t0004g0214a0001c0016t0004g0215others(2): Show | 5 | 254 | 0.0197 | -4 | c.163 others(19): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 2/29 | chr13 | TogoVar | ||||||
ATP11A_chr13_112685038_112892168 | 112804207 | TTCCC | T | intron_variant | MODIFIER | HG06807.hp1 NA19064.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0072 | a0001c0001t0001g0012a0001c0001t0072g0006 | 2 | 254 | 0.0079 | -4 | c.163 others(19): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112805698 | AAAAG | A | intron_variant | MODIFIER | HG01261.hp1 HG02280.hp2 HG02886.hp2 others(1): Show |
a0001a0014 | a0001c0002a0001c0044a0001c0045others(1): Show | a0001c0002t0004a0001c0044t0045a0001c0045t0014others(1): Show | a0001c0002t0004g0041a0001c0044t0045g0133a0001c0045t0014g0254others(1): Show | 4 | 254 | 0.0158 | -4 | c.253 others(19): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112806648 | TTTTG | T | intron_variant | MODIFIER | HG01109.hp1 HG02622.hp2 NA19240.hp1 |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0013 | a0001c0002t0001g0032a0001c0002t0013g0111a0001c0002t0013g0211 | 3 | 254 | 0.0118 | -4 | c.333 others(19): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112811161 | AACAC | A | intron_variant | MODIFIER | HG00438.hp2 HG01069.hp1 HG01071.hp1 others(2): Show |
a0001a0002 | a0001c0002a0002c0003 | a0001c0002t0002a0001c0002t0008a0002c0003t0002 | a0001c0002t0002g0021a0001c0002t0002g0190a0001c0002t0008g0066others(2): Show | 5 | 254 | 0.0197 | -4 | c.441 others(19): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112829953 | GCAAA | G | intron_variant | MODIFIER | HG00738.hp1 HG03239.hp2 HG03834.hp1 |
a0001a0003 | a0001c0001a0001c0002a0003c0007 | a0001c0001t0001a0001c0002t0006a0003c0007t0005 | a0001c0001t0001g0244a0001c0002t0006g0014a0003c0007t0005g0177 | 3 | 254 | 0.0118 | -4 | c.122 others(23): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112831959 | ACACT | A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(113): Show |
a0001a0003a0004others(5): Show | a0001c0001a0001c0002a0001c0005others(19): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(55): Show | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(113): Show | 116 | 254 | 0.4567 | -4 | c.139 others(21): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112832089 | TCACA | T | intron_variant | MODIFIER | HG02132.hp1 NA18942.hp1 NA18995.hp1 others(1): Show |
a0001 | a0001c0005 | a0001c0005t0002a0001c0005t0017a0001c0005t0035 | a0001c0005t0002g0127a0001c0005t0017g0080a0001c0005t0017g0099others(1): Show | 4 | 254 | 0.0158 | -4 | c.139 others(21): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112834467 | CTGTT | C | intron_variant | MODIFIER | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(45): Show |
a0001a0003a0005 | a0001c0004a0001c0006a0001c0024others(6): Show | a0001c0004t0001a0001c0004t0002a0001c0004t0003others(16): Show | a0001c0004t0001g0017a0001c0004t0001g0106a0001c0004t0001g0224others(45): Show | 48 | 254 | 0.1890 | -4 | c.156 others(21): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 14/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112845276 | TATTC | T | intron_variant | MODIFIER | HG01891.hp2 HG02055.hp2 HG03453.hp1 others(1): Show |
a0001 | a0001c0016a0001c0017 | a0001c0016t0004a0001c0017t0058a0001c0017t0076 | a0001c0016t0004g0214a0001c0016t0004g0215a0001c0017t0058g0053others(1): Show | 4 | 254 | 0.0158 | -4 | c.180 others(23): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112845401 | TATTC | T | intron_variant | MODIFIER | HG01891.hp2 HG02055.hp2 HG03453.hp1 others(1): Show |
a0001 | a0001c0016a0001c0017 | a0001c0016t0004a0001c0017t0058a0001c0017t0076 | a0001c0016t0004g0214a0001c0016t0004g0215a0001c0017t0058g0053others(1): Show | 4 | 254 | 0.0158 | -4 | c.180 others(23): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112845464 | TATTC | T | intron_variant | MODIFIER | HG01891.hp2 HG02055.hp2 HG03453.hp1 others(1): Show |
a0001 | a0001c0016a0001c0017 | a0001c0016t0004a0001c0017t0058a0001c0017t0076 | a0001c0016t0004g0214a0001c0016t0004g0215a0001c0017t0058g0053others(1): Show | 4 | 254 | 0.0158 | -4 | c.180 others(23): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112845558 | TAACC | T | intron_variant | MODIFIER | HG01243.hp1 HG01891.hp1 HG02559.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0009 | a0001c0001t0001a0001c0002t0003a0001c0002t0013others(6): Show | a0001c0001t0001g0210a0001c0002t0003g0198a0001c0002t0013g0117others(6): Show | 9 | 254 | 0.0354 | -4 | c.180 others(23): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112845622 | TAACC | T | intron_variant | MODIFIER | HG01243.hp1 HG01891.hp1 HG02559.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0009 | a0001c0001t0001a0001c0002t0003a0001c0002t0013others(6): Show | a0001c0001t0001g0210a0001c0002t0003g0198a0001c0002t0013g0117others(6): Show | 9 | 254 | 0.0354 | -4 | c.180 others(23): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112870931 | GTGTC | G | intron_variant | MODIFIER | HG00558.hp2 HG02083.hp1 HG02523.hp2 others(2): Show |
a0001a0002 | a0001c0001a0002c0010 | a0001c0001t0010a0002c0010t0010 | a0001c0001t0010g0002a0001c0001t0010g0004a0001c0001t0010g0095others(2): Show | 5 | 254 | 0.0197 | -4 | c.299 others(21): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 25/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112875492 | GTTTT | G | intron_variant | MODIFIER | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(108): Show |
a0001a0002a0005others(6): Show | a0001c0001a0001c0002a0001c0006others(23): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(51): Show | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0016others(108): Show | 111 | 254 | 0.4370 | -4 | c.316 others(21): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 27/29 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ATP11A_chr13_112685038_112892168 | 112885235 | TACAC | T | 3_prime_UTR_variant | MODIFIER | HG00544.hp1 HG00639.hp1 HG00642.hp1 others(43): Show |
a0001a0002a0003 | a0001c0002a0001c0004a0001c0009others(11): Show | a0001c0002t0003a0001c0002t0006a0001c0002t0008others(22): Show | a0001c0002t0003g0198a0001c0002t0006g0014a0001c0002t0008g0066others(43): Show | 46 | 254 | 0.1811 | -4 | c.*33 others(15): Show |
ATP11A | ENSG00000068650.19 | transcript | ENST00000375645.8 | protein_coding | 30/30 | 6945 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||
ATP11B_chr3_182788504_182926629 | 182811083 | TAATG | T | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(113): Show |
a0001a0005a0007 | a0001c0001a0005c0006a0007c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(5): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 116 | 324 | 0.3580 | -4 | c.28- others(19): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ATP11B_chr3_182788504_182926629 | 182845006 | ATTTT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(26): Show |
a0001 | a0001c0002 | a0001c0002t0004a0001c0002t0009a0001c0002t0010others(2): Show | a0001c0002t0004g0007a0001c0002t0004g0120a0001c0002t0004g0271others(25): Show | 29 | 324 | 0.0895 | -4 | c.705 others(19): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ATP11B_chr3_182788504_182926629 | 182854752 | TACAC | T | intron_variant | MODIFIER | HG01069.hp1 HG03710.hp1 NA18944.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(1): Show | a0001c0001t0002g0122a0001c0001t0002g0164a0001c0001t0003g0182others(6): Show | 9 | 324 | 0.0278 | -4 | c.852 others(21): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ATP11B_chr3_182788504_182926629 | 182910071 | CAGAA | C | intron_variant | MODIFIER | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(58): Show |
a0001a0006a0008 | a0001c0001a0006c0008a0008c0009 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(4): Show | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0123others(58): Show | 61 | 324 | 0.1883 | -4 | c.331 others(23): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 28/29 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ATP11B_chr3_182788504_182926629 | 182922475 | CCTCT | C | downstream_gene_variant | MODIFIER | HG01109.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0016a0002c0003t0002 | a0001c0001t0016g0173a0002c0003t0002g0116a0002c0003t0002g0117others(2): Show | 5 | 324 | 0.0154 | -4 | c.*43 others(15): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 847 | chr3 | TogoVar | ||||||
ATP11B_chr3_182788504_182926629 | 182923516 | ATAGT | A | downstream_gene_variant | MODIFIER | HG00639.hp1 HG01934.hp1 HG01981.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006a0001c0001t0001g0021a0001c0001t0001g0098others(4): Show | 8 | 324 | 0.0247 | -4 | c.*54 others(15): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 1888 | chr3 | TogoVar | ||||||
ATP11B_chr3_182788504_182926629 | 182923827 | CAAAA | C | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(78): Show |
a0001a0003a0006others(1): Show | a0001c0001a0003c0005a0006c0008others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(5): Show | a0001c0001t0002g0121a0001c0001t0002g0122a0001c0001t0002g0123others(78): Show | 81 | 324 | 0.2500 | -4 | c.*57 others(15): Show |
ATP11B | ENSG00000058063.16 | transcript | ENST00000323116.10 | protein_coding | 2199 | chr3 | TogoVar | ||||||
ATP11C_chrX_139721348_139938053 | 139742874 | AAAAT | A | intron_variant | MODIFIER | HG00639.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0017 | 1 | 234 | 0.0043 | -4 | c.303 others(21): Show |
ATP11C | ENSG00000101974.15 | transcript | ENST00000682941.1 | protein_coding | 26/29 | chrX | TogoVar | ||||||
ATP11C_chrX_139721348_139938053 | 139769281 | CATAT | C | intron_variant | MODIFIER | HG02280.hp1 HG02723.hp2 HG02738.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0013a0001c0001t0034 | a0001c0001t0001g0087a0001c0001t0001g0105a0001c0001t0001g0149others(4): Show | 7 | 234 | 0.0299 | -4 | c.221 others(21): Show |
ATP11C | ENSG00000101974.15 | transcript | ENST00000682941.1 | protein_coding | 19/29 | chrX | TogoVar | ||||||
ATP11C_chrX_139721348_139938053 | 139786278 | GTATT | G | intron_variant | MODIFIER | HG00639.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0017 | 1 | 234 | 0.0043 | -4 | c.159 others(21): Show |
ATP11C | ENSG00000101974.15 | transcript | ENST00000682941.1 | protein_coding | 15/29 | chrX | TogoVar | ||||||
ATP11C_chrX_139721348_139938053 | 139790464 | TCACA | T | intron_variant | MODIFIER | HG00639.hp2 HG01109.hp1 HG01167.hp1 others(15): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(1): Show | a0001c0001t0001g0077a0001c0001t0001g0134a0001c0001t0001g0147others(15): Show | 18 | 234 | 0.0769 | -4 | c.120 others(21): Show |
ATP11C | ENSG00000101974.15 | transcript | ENST00000682941.1 | protein_coding | 12/29 | chrX | TogoVar | ||||||
ATP11C_chrX_139721348_139938053 | 139796999 | TTTTC | T | intron_variant | MODIFIER | HG01891.hp2 HG02723.hp1 HG02886.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0021a0001c0001t0003g0022a0001c0001t0003g0023others(1): Show | 4 | 234 | 0.0171 | -4 | c.100 others(21): Show |
ATP11C | ENSG00000101974.15 | transcript | ENST00000682941.1 | protein_coding | 11/29 | chrX | TogoVar | ||||||
ATP11C_chrX_139721348_139938053 | 139814329 | AGTGG | A | intron_variant | MODIFIER | HG02965.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0199 | 1 | 234 | 0.0043 | -4 | c.426 others(19): Show |
ATP11C | ENSG00000101974.15 | transcript | ENST00000682941.1 | protein_coding | 5/29 | chrX | TogoVar | ||||||
ATP11C_chrX_139721348_139938053 | 139841904 | CCTAG | C | intron_variant | MODIFIER | NA18948.hp1 NA19070.hp1 NA19081.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0100a0001c0001t0001g0112a0001c0001t0001g0174 | 3 | 234 | 0.0128 | -4 | c.28- others(21): Show |
ATP11C | ENSG00000101974.15 | transcript | ENST00000682941.1 | protein_coding | 1/29 | chrX | TogoVar | ||||||
ATP11C_chrX_139721348_139938053 | 139852450 | TGCGG | T | intron_variant | MODIFIER | HG01981.hp2 HG02004.hp2 HG02083.hp1 others(7): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0002a0001c0003t0002a0002c0002t0002others(2): Show | a0001c0001t0002g0177a0001c0001t0002g0181a0001c0001t0002g0190others(7): Show | 10 | 234 | 0.0427 | -4 | c.28- others(21): Show |
ATP11C | ENSG00000101974.15 | transcript | ENST00000682941.1 | protein_coding | 1/29 | chrX | TogoVar | ||||||
ATP11C_chrX_139721348_139938053 | 139852452 | CGGGG | C | intron_variant | MODIFIER | HG01358.hp1 HG01433.hp1 HG02015.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0115others(4): Show | 7 | 234 | 0.0299 | -4 | c.28- others(21): Show |
ATP11C | ENSG00000101974.15 | transcript | ENST00000682941.1 | protein_coding | 1/29 | chrX | TogoVar | ||||||
ATP11C_chrX_139721348_139938053 | 139852478 | GGGGA | G | intron_variant | MODIFIER | NA19009.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0049 | 1 | 234 | 0.0043 | -4 | c.28- others(21): Show |
ATP11C | ENSG00000101974.15 | transcript | ENST00000682941.1 | protein_coding | 1/29 | chrX | TogoVar | ||||||
ATP11C_chrX_139721348_139938053 | 139853337 | AAGAC | A | intron_variant | MODIFIER | NA19072.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0114 | 1 | 234 | 0.0043 | -4 | c.28- others(21): Show |
ATP11C | ENSG00000101974.15 | transcript | ENST00000682941.1 | protein_coding | 1/29 | chrX | TogoVar | ||||||
ATP11C_chrX_139721348_139938053 | 139861672 | GGACT | G | intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0209 | 1 | 234 | 0.0043 | -4 | c.28- others(21): Show |
ATP11C | ENSG00000101974.15 | transcript | ENST00000682941.1 | protein_coding | 1/29 | chrX | TogoVar | ||||||
ATP11C_chrX_139721348_139938053 | 139861769 | TACAC | T | intron_variant | MODIFIER | HG01109.hp1 HG01167.hp1 HG01169.hp2 others(18): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(3): Show | a0001c0001t0002g0191a0001c0001t0003g0207a0001c0001t0004g0062others(18): Show | 21 | 234 | 0.0897 | -4 | c.28- others(21): Show |
ATP11C | ENSG00000101974.15 | transcript | ENST00000682941.1 | protein_coding | 1/29 | chrX | TogoVar |