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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ACP3_chr3_132312407_132363841 | 132324626 | AATT | A | intron_variant | MODIFIER | HG01884.hp2 HG02258.hp1 HG02572.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0009a0001c0002t0003a0001c0002t0004others(1): Show | a0001c0001t0009g0010a0001c0002t0003g0065a0001c0002t0003g0116others(4): Show | 9 | 368 | 0.0245 | -3 | c.121 others(20): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP3_chr3_132312407_132363841 | 132350184 | CAAG | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(114): Show |
a0001a0003 | a0001c0002a0001c0003a0003c0006 | a0001c0002t0003a0001c0002t0004a0001c0002t0011others(9): Show | a0001c0002t0003g0011a0001c0002t0003g0039a0001c0002t0003g0051others(107): Show | 117 | 368 | 0.3179 | -3 | c.864 others(18): Show |
ACP3 | ENSG00000014257.17 | transcript | ENST00000336375.10 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ACP4_chr19_50785415_50800219 | 50790456 | CCTG | C | conservative_inframe_deletion | MODERATE | HG01884.hp1 HG02647.hp1 HG02809.hp2 |
a0004 | a0004c0006 | a0004c0006t0001 | a0004c0006t0001g0023a0004c0006t0001g0049 | 3 | 380 | 0.0079 | -3 | c.58_ others(8): Show |
p.Leu others(5): Show |
ACP4 | ENSG00000142513.6 | transcript | ENST00000270593.2 | protein_coding | 1/11 | 58/1342 | 58/1281 | 20/426 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |
ACP4_chr19_50785415_50800219 | 50793523 | AAAC | A | intron_variant | MODIFIER | HG02145.hp2 HG02486.hp1 HG02970.hp2 others(2): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0001 | a0001c0001t0001g0033a0001c0005t0001g0015 | 5 | 380 | 0.0132 | -3 | c.646 others(18): Show |
ACP4 | ENSG00000142513.6 | transcript | ENST00000270593.2 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACP5_chr19_11569660_11582645 | 11579309 | TCTC | T | upstream_gene_variant | MODIFIER | HG00323.hp2 HG01168.hp1 HG01358.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0017a0001c0001t0001g0066a0001c0001t0001g0067 | 4 | 444 | 0.0090 | -3 | c.-17 others(14): Show |
ACP5 | ENSG00000102575.14 | transcript | ENST00000648477.1 | protein_coding | 1665 | chr19 | TogoVar | ||||||
ACP5_chr19_11569660_11582645 | 11580738 | CAAA | C | upstream_gene_variant | MODIFIER | HG00438.hp1 HG00544.hp1 HG01175.hp2 others(27): Show |
a0001a0004a0010 | a0001c0001a0001c0004a0004c0006others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0004t0001others(2): Show | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0010others(16): Show | 30 | 444 | 0.0676 | -3 | c.-31 others(14): Show |
ACP5 | ENSG00000102575.14 | transcript | ENST00000648477.1 | protein_coding | 3094 | chr19 | TogoVar | ||||||
ACP6_chr1_147637230_147675524 | 147642918 | GAAA | G | 3_prime_UTR_variant | MODIFIER | HG02630.hp1 HG02723.hp1 HG02976.hp2 others(2): Show |
a0001 | a0001c0003 | a0001c0003t0018a0001c0003t0039a0001c0003t0040 | a0001c0003t0018g0046a0001c0003t0018g0182a0001c0003t0039g0097others(1): Show | 5 | 404 | 0.0124 | -3 | c.*45 others(14): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 10/10 | 4502 | chr1 | TogoVar | |||||
ACP6_chr1_147637230_147675524 | 147659547 | AAAG | A | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(23): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0011a0001c0001t0034a0001c0002t0029others(8): Show | a0001c0001t0011g0018a0001c0001t0011g0056a0001c0001t0034g0049others(14): Show | 26 | 404 | 0.0644 | -3 | c.349 others(16): Show |
ACP6 | ENSG00000162836.12 | transcript | ENST00000583509.7 | protein_coding | 2/9 | chr1 | TogoVar | ||||||
ACP7_chr19_39079368_39116493 | 39098253 | CAAA | C | intron_variant | MODIFIER | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(108): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0005others(6): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(18): Show | a0001c0001t0001g0339a0001c0001t0006g0136a0001c0001t0014g0137others(108): Show | 111 | 402 | 0.2761 | -3 | c.122 others(18): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACP7_chr19_39079368_39116493 | 39103441 | GTTT | G | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(92): Show |
a0001 | a0001c0001a0001c0002a0001c0009others(2): Show | a0001c0001t0001a0001c0001t0011a0001c0002t0002others(13): Show | a0001c0001t0001g0378a0001c0001t0001g0398a0001c0001t0011g0183others(92): Show | 95 | 402 | 0.2363 | -3 | c.111 others(22): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACP7_chr19_39079368_39116493 | 39108139 | ATTT | A | intron_variant | MODIFIER | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
a0001a0002a0004 | a0001c0001a0001c0004a0001c0006others(5): Show | a0001c0001t0004a0001c0004t0004a0001c0004t0009others(9): Show | a0001c0001t0004g0327a0001c0001t0004g0374a0001c0004t0004g0033others(60): Show | 63 | 402 | 0.1567 | -3 | c.125 others(22): Show |
ACP7 | ENSG00000183760.11 | transcript | ENST00000331256.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACRBP_chr12_6633075_6652432 | 6645960 | CTGT | C | intron_variant | MODIFIER | HG01255.hp2 NA19011.hp1 NA19072.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0028a0001c0001t0002g0042 | 3 | 422 | 0.0071 | -3 | c.357 others(18): Show |
ACRBP | ENSG00000111644.8 | transcript | ENST00000229243.7 | protein_coding | 3/9 | chr12 | TogoVar | ||||||
ACR_chr22_50733204_50750339 | 50742543 | CAAA | C | intron_variant | MODIFIER | HG00280.hp1 HG00733.hp1 HG01346.hp1 others(25): Show |
a0001a0002a0009 | a0001c0001a0002c0002a0009c0010 | a0001c0001t0001a0002c0002t0001a0009c0010t0001 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0030others(12): Show | 28 | 464 | 0.0603 | -3 | c.566 others(20): Show |
ACR | ENSG00000100312.11 | transcript | ENST00000216139.10 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ACSBG1_chr15_78162468_78239565 | 78235935 | AAAC | A | upstream_gene_variant | MODIFIER | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(90): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0006a0001c0008others(12): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0013others(26): Show | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0067others(89): Show | 93 | 350 | 0.2657 | -3 | c.-14 others(14): Show |
ACSBG1 | ENSG00000103740.10 | transcript | ENST00000258873.9 | protein_coding | 1371 | chr15 | TogoVar | ||||||
ACSBG1_chr15_78162468_78239565 | 78238217 | GCCT | G | upstream_gene_variant | MODIFIER | HG01255.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0003others(1): Show | a0001c0001t0001a0002c0002t0004a0002c0003t0015others(1): Show | a0001c0001t0001g0050a0002c0002t0004g0053a0002c0002t0004g0054others(7): Show | 10 | 350 | 0.0286 | -3 | c.-37 others(14): Show |
ACSBG1 | ENSG00000103740.10 | transcript | ENST00000258873.9 | protein_coding | 3653 | chr15 | TogoVar | ||||||
ACSBG2_chr19_6130667_6198091 | 6137209 | TGGG | T | intron_variant | MODIFIER | HG01934.hp1 HG02129.hp1 HG02145.hp1 others(21): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0011others(2): Show | a0001c0001t0001a0001c0001t0003a0002c0002t0001others(3): Show | a0001c0001t0001g0015a0001c0001t0001g0139a0001c0001t0001g0140others(21): Show | 24 | 262 | 0.0916 | -3 | c.-32 others(20): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6138553 | GGAA | G | intron_variant | MODIFIER | HG01934.hp1 HG02145.hp1 HG02647.hp2 others(12): Show |
a0002a0005 | a0002c0002a0005c0006 | a0002c0002t0001a0005c0006t0001 | a0002c0002t0001g0019a0002c0002t0001g0020a0002c0002t0001g0021others(12): Show | 15 | 262 | 0.0573 | -3 | c.-32 others(20): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6143972 | TTTG | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
a0001a0003a0004others(4): Show | a0001c0001a0001c0017a0001c0020others(9): Show | a0001c0001t0001a0001c0017t0001a0001c0020t0001others(9): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(134): Show | 138 | 262 | 0.5267 | -3 | c.67+ others(18): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6149504 | CTTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
a0001a0003a0014others(1): Show | a0001c0001a0001c0017a0001c0024others(3): Show | a0001c0001t0001a0001c0017t0001a0001c0024t0001others(3): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(112): Show | 115 | 262 | 0.4389 | -3 | c.297 others(20): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6155789 | CAAA | C | intron_variant | MODIFIER | HG01433.hp1 NA18973.hp2 NA18975.hp2 others(4): Show |
a0003 | a0003c0005 | a0003c0005t0001 | a0003c0005t0001g0001a0003c0005t0001g0133a0003c0005t0001g0241others(3): Show | 7 | 262 | 0.0267 | -3 | c.387 others(18): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6162566 | CAAA | C | intron_variant | MODIFIER | HG01071.hp2 HG02055.hp2 HG02080.hp1 others(16): Show |
a0001a0003a0004others(3): Show | a0001c0020a0003c0004a0003c0012others(5): Show | a0001c0020t0001a0003c0004t0002a0003c0012t0002others(5): Show | a0001c0020t0001g0051a0003c0004t0002g0006a0003c0004t0002g0007others(16): Show | 19 | 262 | 0.0725 | -3 | c.588 others(20): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6163121 | AAAT | A | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(104): Show |
a0001a0002a0003others(6): Show | a0001c0001a0002c0002a0003c0004others(8): Show | a0001c0001t0001a0002c0002t0001a0003c0004t0002others(8): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 107 | 262 | 0.4084 | -3 | c.588 others(20): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6163783 | CAAA | C | intron_variant | MODIFIER | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
a0001a0003a0004others(5): Show | a0001c0001a0001c0020a0003c0005others(8): Show | a0001c0001t0001a0001c0020t0001a0003c0005t0001others(8): Show | a0001c0001t0001g0015a0001c0020t0001g0051a0003c0005t0001g0001others(19): Show | 23 | 262 | 0.0878 | -3 | c.589 others(20): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6166328 | GTGT | G | intron_variant | MODIFIER | HG01433.hp2 HG01496.hp1 HG02602.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004a0001c0001t0001g0038a0001c0001t0001g0179others(1): Show | 4 | 262 | 0.0153 | -3 | c.738 others(18): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6171824 | TTTC | T | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
a0003a0004a0007others(3): Show | a0003c0011a0004c0003a0007c0008others(3): Show | a0003c0011t0001a0004c0003t0002a0007c0008t0002others(3): Show | a0003c0011t0001g0144a0003c0011t0001g0160a0004c0003t0002g0134others(12): Show | 15 | 262 | 0.0573 | -3 | c.739 others(20): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6174810 | CTCA | C | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(12): Show |
a0003a0004a0007others(3): Show | a0003c0011a0004c0003a0007c0008others(3): Show | a0003c0011t0001a0004c0003t0002a0007c0008t0002others(3): Show | a0003c0011t0001g0144a0003c0011t0001g0160a0004c0003t0002g0134others(12): Show | 15 | 262 | 0.0573 | -3 | c.739 others(20): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6177739 | CTTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
a0001a0002a0018 | a0001c0001a0001c0024a0002c0002others(1): Show | a0001c0001t0001a0001c0024t0001a0002c0002t0001others(1): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(102): Show | 105 | 262 | 0.4008 | -3 | c.906 others(18): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6178373 | CATT | C | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp2 HG01433.hp1 others(37): Show |
a0003a0004a0007others(3): Show | a0003c0004a0003c0005a0003c0011others(7): Show | a0003c0004t0002a0003c0005t0001a0003c0011t0001others(8): Show | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(36): Show | 40 | 262 | 0.1527 | -3 | c.906 others(19): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6179293 | ATTT | A | intron_variant | MODIFIER | HG01433.hp1 HG02055.hp2 HG02109.hp1 others(16): Show |
a0003a0009 | a0003c0004a0003c0005a0003c0012others(1): Show | a0003c0004t0002a0003c0005t0001a0003c0012t0002others(1): Show | a0003c0004t0002g0006a0003c0004t0002g0007a0003c0004t0002g0008others(15): Show | 19 | 262 | 0.0725 | -3 | c.906 others(20): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6184832 | GAAA | G | intron_variant | MODIFIER | HG01074.hp1 HG01168.hp1 HG01891.hp2 others(3): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0007 | a0001c0001t0001a0001c0001t0003a0002c0002t0001others(1): Show | a0001c0001t0001g0016a0001c0001t0001g0182a0001c0001t0003g0141others(3): Show | 6 | 262 | 0.0229 | -3 | c.132 others(20): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ACSBG2_chr19_6130667_6198091 | 6197275 | CAAA | C | downstream_gene_variant | MODIFIER | HG02145.hp1 HG02615.hp1 HG02886.hp2 others(2): Show |
a0001a0005 | a0001c0001a0005c0006 | a0001c0001t0003a0005c0006t0001 | a0001c0001t0003g0141a0001c0001t0003g0143a0001c0001t0003g0146others(2): Show | 5 | 262 | 0.0191 | -3 | c.*46 others(14): Show |
ACSBG2 | ENSG00000130377.14 | transcript | ENST00000588485.6 | protein_coding | 4185 | chr19 | TogoVar | ||||||
ACSF3_chr16_89088852_89161233 | 89131124 | TTTC | T | intron_variant | MODIFIER | HG02300.hp1 HG02683.hp2 HG03654.hp1 others(7): Show |
a0002a0003a0006others(1): Show | a0002c0002a0003c0006a0003c0010others(2): Show | a0002c0002t0004a0002c0002t0006a0002c0002t0014others(4): Show | a0002c0002t0004g0225a0002c0002t0006g0065a0002c0002t0006g0134others(7): Show | 10 | 368 | 0.0272 | -3 | c.124 others(22): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ACSF3_chr16_89088852_89161233 | 89131127 | CTTT | C | intron_variant | MODIFIER | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(29): Show |
a0002a0005 | a0002c0002a0002c0003a0005c0009 | a0002c0002t0004a0002c0003t0005a0002c0003t0021others(5): Show | a0002c0002t0004g0126a0002c0003t0005g0015a0002c0003t0005g0016others(29): Show | 32 | 368 | 0.0870 | -3 | c.124 others(22): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ACSF3_chr16_89088852_89161233 | 89145922 | GTTC | G | intron_variant | MODIFIER | HG00621.hp1 NA18995.hp2 NA19003.hp1 others(2): Show |
a0002 | a0002c0002 | a0002c0002t0006 | a0002c0002t0006g0108a0002c0002t0006g0135a0002c0002t0006g0142others(2): Show | 5 | 368 | 0.0136 | -3 | c.150 others(17): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ACSF3_chr16_89088852_89161233 | 89149513 | CTGG | C | intron_variant | MODIFIER | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(66): Show |
a0001a0002a0005others(2): Show | a0001c0001a0002c0002a0002c0003others(4): Show | a0001c0001t0001a0001c0001t0015a0002c0002t0004others(17): Show | a0001c0001t0001g0098a0001c0001t0015g0100a0002c0002t0004g0118others(66): Show | 69 | 368 | 0.1875 | -3 | c.161 others(22): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | chr16 | TogoVar | ||||||
ACSF3_chr16_89088852_89161233 | 89151609 | ATAT | A | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(29): Show |
a0002a0004 | a0002c0003a0004c0004 | a0002c0003t0040a0004c0004t0003a0004c0004t0022others(3): Show | a0002c0003t0040g0060a0004c0004t0003g0005a0004c0004t0003g0014others(28): Show | 32 | 368 | 0.0870 | -3 | c.161 others(22): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |||||
ACSF3_chr16_89088852_89161233 | 89158506 | ACAC | A | downstream_gene_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(25): Show |
a0002a0003a0008 | a0002c0002a0003c0006a0003c0007others(2): Show | a0002c0002t0007a0003c0006t0007a0003c0006t0048others(4): Show | a0002c0002t0007g0109a0003c0006t0007g0001a0003c0006t0007g0017others(24): Show | 28 | 368 | 0.0761 | -3 | c.*43 others(14): Show |
ACSF3 | ENSG00000176715.17 | transcript | ENST00000614302.5 | protein_coding | 2274 | chr16 | TogoVar | ||||||
ACSL1_chr4_184750595_184830968 | 184752197 | ATGT | A | downstream_gene_variant | MODIFIER | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(162): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(8): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(152): Show | 165 | 392 | 0.4209 | -3 | c.*49 others(14): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 3397 | chr4 | TogoVar | ||||||
ACSL1_chr4_184750595_184830968 | 184781229 | CAAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(12): Show | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0047others(137): Show | 147 | 392 | 0.3750 | -3 | c.376 others(18): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 4/20 | chr4 | TogoVar | ||||||
ACSL1_chr4_184750595_184830968 | 184814290 | CAAA | C | intron_variant | MODIFIER | HG01891.hp1 HG02486.hp1 HG02809.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0002t0002others(1): Show | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0354others(5): Show | 8 | 392 | 0.0204 | -3 | c.-32 others(22): Show |
ACSL1 | ENSG00000151726.16 | transcript | ENST00000281455.7 | protein_coding | 1/20 | chr4 | TogoVar | ||||||
ACSL3_chr2_222856036_222949639 | 222866753 | GCCC | G | intron_variant | MODIFIER | HG00639.hp2 HG01168.hp1 HG01256.hp2 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0003a0001c0001t0001g0031a0001c0001t0001g0032others(14): Show | 18 | 252 | 0.0714 | -3 | c.-20 others(22): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACSL3_chr2_222856036_222949639 | 222878752 | GTTC | G | intron_variant | MODIFIER | HG00423.hp1 HG01358.hp1 HG02155.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0015 | a0001c0001t0002g0161a0001c0001t0002g0218a0001c0001t0002g0219others(4): Show | 7 | 252 | 0.0278 | -3 | c.-20 others(22): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACSL3_chr2_222856036_222949639 | 222886163 | CCAT | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(231): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0006others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 234 | 252 | 0.9286 | -3 | c.-20 others(22): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACSL3_chr2_222856036_222949639 | 222895470 | CTTT | C | intron_variant | MODIFIER | HG00280.hp2 HG01346.hp2 HG01433.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0019 | a0001c0001t0006g0130a0001c0001t0006g0133a0001c0001t0006g0134others(3): Show | 6 | 252 | 0.0238 | -3 | c.-14 others(22): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACSL3_chr2_222856036_222949639 | 222900231 | GAAT | G | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0017a0001c0001t0024others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(79): Show | 85 | 252 | 0.3373 | -3 | c.-14 others(20): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACSL3_chr2_222856036_222949639 | 222929923 | CTTT | C | intron_variant | MODIFIER | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(5): Show |
a0001 | a0001c0002 | a0001c0002t0005 | a0001c0002t0005g0121a0001c0002t0005g0122a0001c0002t0005g0123others(5): Show | 8 | 252 | 0.0318 | -3 | c.154 others(20): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACSL3_chr2_222856036_222949639 | 222937200 | ATTG | A | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(223): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0006others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(220): Show | 226 | 252 | 0.8968 | -3 | c.200 others(22): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACSL3_chr2_222856036_222949639 | 222937514 | TATC | T | intron_variant | MODIFIER | HG00323.hp1 HG01256.hp1 HG01258.hp1 others(4): Show |
a0001 | a0001c0002 | a0001c0002t0005 | a0001c0002t0005g0121a0001c0002t0005g0122a0001c0002t0005g0123others(4): Show | 7 | 252 | 0.0278 | -3 | c.200 others(22): Show |
ACSL3 | ENSG00000123983.15 | transcript | ENST00000357430.8 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACSL4_chrX_109636335_109738257 | 109666386 | TAAG | T | intron_variant | MODIFIER | HG02559.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0203 | 1 | 222 | 0.0045 | -3 | c.131 others(20): Show |
ACSL4 | ENSG00000068366.21 | transcript | ENST00000672401.1 | protein_coding | 11/15 | chrX | TogoVar | ||||||
ACSL4_chrX_109636335_109738257 | 109685088 | CTTT | C | intron_variant | MODIFIER | HG02647.hp1 HG02886.hp2 HG03225.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0189a0001c0001t0003g0190a0001c0001t0003g0191others(2): Show | 5 | 222 | 0.0225 | -3 | c.-12 others(20): Show |
ACSL4 | ENSG00000068366.21 | transcript | ENST00000672401.1 | protein_coding | 2/15 | chrX | TogoVar |