| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| A1CF_chr10_50794409_50890627 | 50832047 | G | A | intron_variant | MODIFIER | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0037 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | 338 | 0.0148 | 0 | c.605 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50832114 | C | T | intron_variant | MODIFIER | NA18954.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0230 | 1 | 338 | 0.0030 | 0 | c.605 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50832185 | T | C | intron_variant | MODIFIER | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
a0001a0002 | a0001c0008a0002c0006 | a0001c0008t0001a0001c0008t0017a0002c0006t0006 | a0001c0008t0001g0039a0001c0008t0017g0042a0002c0006t0006g0044others(2): Show | 5 | 338 | 0.0148 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50832227 | G | T | intron_variant | MODIFIER | HG00621.hp2 NA19065.hp1 NA19077.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0035 | a0001c0001t0002g0027a0001c0001t0035g0155 | 3 | 338 | 0.0089 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50832253 | G | A | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0009a0001c0001t0015a0001c0001t0043others(1): Show | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(4): Show | 8 | 338 | 0.0237 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50832390 | A | C | intron_variant | MODIFIER | HG02258.hp2 HG03516.hp2 |
a0001 | a0001c0007 | a0001c0007t0005a0001c0007t0033 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | 338 | 0.0059 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50832494 | C | T | intron_variant | MODIFIER | HG00423.hp2 HG00597.hp2 HG01109.hp2 others(33): Show |
a0001 | a0001c0001a0001c0002a0001c0009 | a0001c0001t0001a0001c0001t0005a0001c0001t0012others(4): Show | a0001c0001t0001g0074a0001c0001t0005g0251a0001c0001t0005g0253others(29): Show | 36 | 338 | 0.1065 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50832505 | A | G | intron_variant | MODIFIER | NA18906.hp2 | a0002 | a0002c0006 | a0002c0006t0006 | a0002c0006t0006g0044 | 1 | 338 | 0.0030 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50832569 | T | A | intron_variant | MODIFIER | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0037 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | 338 | 0.0148 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50832606 | T | G | intron_variant | MODIFIER | HG02015.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0186 | 1 | 338 | 0.0030 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50832700 | A | T | intron_variant | MODIFIER | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
a0001a0002 | a0001c0008a0002c0006 | a0001c0008t0001a0001c0008t0017a0002c0006t0006 | a0001c0008t0001g0039a0001c0008t0017g0042a0002c0006t0006g0044others(2): Show | 5 | 338 | 0.0148 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50832839 | C | A | intron_variant | MODIFIER | HG02258.hp2 HG03516.hp2 |
a0001 | a0001c0007 | a0001c0007t0005a0001c0007t0033 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | 338 | 0.0059 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50832867 | GT | G | intron_variant | MODIFIER | HG01069.hp2 HG01884.hp2 HG01891.hp2 others(16): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0003a0001c0001t0008a0001c0001t0009others(7): Show | a0001c0001t0003g0014a0001c0001t0008g0006a0001c0001t0008g0098others(12): Show | 19 | 338 | 0.0562 | -1 | c.604 others(9): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50832873 | T | G | intron_variant | MODIFIER | HG02258.hp2 HG03516.hp2 |
a0001 | a0001c0007 | a0001c0007t0005a0001c0007t0033 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | 338 | 0.0059 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50832918 | T | C | intron_variant | MODIFIER | HG00544.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0119 | 1 | 338 | 0.0030 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50833143 | A | T | intron_variant | MODIFIER | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0037 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | 338 | 0.0148 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50833298 | G | A | intron_variant | MODIFIER | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0037 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | 338 | 0.0148 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50833477 | G | C | intron_variant | MODIFIER | HG02735.hp1 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0081 | 1 | 338 | 0.0030 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50833661 | G | T | intron_variant | MODIFIER | HG00438.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0192 | 1 | 338 | 0.0030 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50834010 | T | C | intron_variant | MODIFIER | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(75): Show |
a0001 | a0001c0001a0001c0003a0001c0011 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0004a0001c0001t0001g0169a0001c0001t0001g0189others(61): Show | 78 | 338 | 0.2308 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50834107 | C | T | intron_variant | MODIFIER | HG02886.hp2 HG03540.hp2 |
a0002 | a0002c0004 | a0002c0004t0018 | a0002c0004t0018g0034a0002c0004t0018g0153 | 2 | 338 | 0.0059 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50834266 | A | G | intron_variant | MODIFIER | HG02258.hp2 HG03516.hp2 |
a0001 | a0001c0007 | a0001c0007t0005a0001c0007t0033 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | 338 | 0.0059 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50834479 | G | T | intron_variant | MODIFIER | HG02258.hp2 HG03516.hp2 |
a0001 | a0001c0007 | a0001c0007t0005a0001c0007t0033 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | 338 | 0.0059 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50834503 | G | C | intron_variant | MODIFIER | NA20129.hp1 | a0002 | a0002c0004 | a0002c0004t0044 | a0002c0004t0044g0049 | 1 | 338 | 0.0030 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50834592 | G | C | intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0223 | 1 | 338 | 0.0030 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50834629 | A | G | intron_variant | MODIFIER | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
a0001a0002 | a0001c0008a0002c0006 | a0001c0008t0001a0001c0008t0017a0002c0006t0006 | a0001c0008t0001g0039a0001c0008t0017g0042a0002c0006t0006g0044others(2): Show | 5 | 338 | 0.0148 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50834680 | C | T | intron_variant | MODIFIER | NA19083.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0138 | 1 | 338 | 0.0030 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50834690 | G | A | intron_variant | MODIFIER | HG02258.hp2 HG03516.hp2 |
a0001 | a0001c0007 | a0001c0007t0005a0001c0007t0033 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | 338 | 0.0059 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50834755 | T | C | intron_variant | MODIFIER | HG02015.hp1 NA18977.hp2 NA19004.hp2 others(1): Show |
a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0071a0001c0002t0004g0076a0001c0002t0004g0077others(1): Show | 4 | 338 | 0.0118 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50834768 | G | T | intron_variant | MODIFIER | HG01981.hp2 HG03139.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0041a0001c0002t0004 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | 338 | 0.0059 | 0 | c.604 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50835087 | A | G | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp1 HG00735.hp1 others(23): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0011a0001c0001t0002g0056a0001c0001t0003g0012others(16): Show | 26 | 338 | 0.0769 | 0 | c.604 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50835111 | A | G | intron_variant | MODIFIER | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
a0001a0002 | a0001c0008a0002c0006 | a0001c0008t0001a0001c0008t0017a0002c0006t0006 | a0001c0008t0001g0039a0001c0008t0017g0042a0002c0006t0006g0044others(2): Show | 5 | 338 | 0.0148 | 0 | c.604 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50835133 | A | G | intron_variant | MODIFIER | HG01884.hp2 NA19043.hp1 |
a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0158a0001c0001t0009g0159 | 2 | 338 | 0.0059 | 0 | c.604 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50835230 | A | G | intron_variant | MODIFIER | homoSapiens_chm13v2.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0117 | 1 | 338 | 0.0030 | 0 | c.604 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50835355 | G | A | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(69): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0010 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 72 | 338 | 0.2130 | 0 | c.604 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50835494 | G | A | intron_variant | MODIFIER | HG02258.hp2 HG03516.hp2 |
a0001 | a0001c0007 | a0001c0007t0005a0001c0007t0033 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | 338 | 0.0059 | 0 | c.604 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50835805 | CTCTT | C | intron_variant | MODIFIER | HG02451.hp2 HG02897.hp2 NA18906.hp1 others(2): Show |
a0001a0002 | a0001c0008a0002c0006 | a0001c0008t0001a0001c0008t0017a0002c0006t0006 | a0001c0008t0001g0039a0001c0008t0017g0042a0002c0006t0006g0044others(2): Show | 5 | 338 | 0.0148 | -4 | c.604 others(19): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50835884 | T | A | intron_variant | MODIFIER | HG02015.hp1 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0080 | 1 | 338 | 0.0030 | 0 | c.604 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50835886 | A | T | intron_variant | MODIFIER | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0037 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | 338 | 0.0148 | 0 | c.604 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50835970 | A | G | intron_variant | MODIFIER | HG02132.hp1 NA19079.hp2 NA19087.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0175a0001c0001t0002g0176a0001c0001t0002g0224 | 3 | 338 | 0.0089 | 0 | c.604 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50835988 | CA | C | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(19): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0007others(2): Show | a0001c0001t0008a0001c0001t0009a0001c0001t0015others(9): Show | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(16): Show | 22 | 338 | 0.0651 | -1 | c.604 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50836380 | G | C | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0009a0001c0001t0015a0001c0001t0041others(2): Show | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(6): Show | 10 | 338 | 0.0296 | 0 | c.366 others(6): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50836539 | T | A | intron_variant | MODIFIER | HG02257.hp1 | a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0266 | 1 | 338 | 0.0030 | 0 | c.366 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50836590 | G | A | intron_variant | MODIFIER | NA19002.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0113 | 1 | 338 | 0.0030 | 0 | c.366 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50836721 | A | G | intron_variant | MODIFIER | HG03486.hp1 | a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0041 | 1 | 338 | 0.0030 | 0 | c.366 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50836795 | T | C | intron_variant | MODIFIER | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(52): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(8): Show | a0001c0001t0001g0225a0001c0001t0001g0276a0001c0001t0003g0018others(43): Show | 55 | 338 | 0.1627 | 0 | c.366 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50837015 | T | C | intron_variant | MODIFIER | HG03195.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0066 | 1 | 338 | 0.0030 | 0 | c.366 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50837021 | C | T | intron_variant | MODIFIER | HG02258.hp2 HG03516.hp2 |
a0001 | a0001c0007 | a0001c0007t0005a0001c0007t0033 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | 338 | 0.0059 | 0 | c.366 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50837297 | C | T | intron_variant | MODIFIER | NA19081.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0148 | 1 | 338 | 0.0030 | 0 | c.366 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | TogoVar | ||||||
| A1CF_chr10_50794409_50890627 | 50837406 | T | C | intron_variant | MODIFIER | HG03831.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0282 | 1 | 338 | 0.0030 | 0 | c.366 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 5/12 | chr10 | TogoVar |