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 | 50815888 | A | G | intron_variant | MODIFIER | NA19076.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0218 | 1 | 338 | 0.0030 | 0 | c.114 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50815930 | A | G | intron_variant | MODIFIER | HG00741.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0125 | 1 | 338 | 0.0030 | 0 | c.114 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50816307 | C | T | intron_variant | MODIFIER | HG04184.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0281 | 1 | 338 | 0.0030 | 0 | c.868 others(6): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50816308 | G | A | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(45): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(244): Show | 292 | 338 | 0.8639 | 0 | c.868 others(6): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50816354 | T | C | intron_variant | MODIFIER | HG00544.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0195 | 1 | 338 | 0.0030 | 0 | c.868 others(6): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50816459 | G | A | intron_variant | MODIFIER | HG01069.hp2 | a0001 | a0001c0001 | a0001c0001t0028 | a0001c0001t0028g0052 | 1 | 338 | 0.0030 | 0 | c.868 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50816670 | A | G | intron_variant | MODIFIER | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(40): Show |
a0001 | a0001c0001a0001c0002a0001c0009others(1): Show | a0001c0001t0005a0001c0001t0016a0001c0002t0004others(3): Show | a0001c0001t0005g0010a0001c0001t0016g0040a0001c0001t0016g0041others(33): Show | 43 | 338 | 0.1272 | 0 | c.868 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50816728 | T | A | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0020others(15): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(96): Show | 116 | 338 | 0.3432 | 0 | c.868 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50816782 | C | T | intron_variant | MODIFIER | HG00438.hp1 HG02602.hp1 HG03942.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0107a0001c0001t0005g0262a0001c0001t0005g0273others(1): Show | 4 | 338 | 0.0118 | 0 | c.868 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50816830 | T | C | intron_variant | MODIFIER | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0004others(1): Show | a0001c0001t0017a0001c0008t0017a0002c0004t0006others(4): Show | a0001c0001t0017g0266a0001c0008t0017g0042a0002c0004t0006g0032others(10): Show | 14 | 338 | 0.0414 | 0 | c.868 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50817113 | G | A | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(109): Show |
a0001 | a0001c0001a0001c0007a0001c0011 | a0001c0001t0002a0001c0001t0003a0001c0001t0011others(11): Show | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0027others(90): Show | 112 | 338 | 0.3314 | 0 | c.868 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50817296 | A | C | intron_variant | MODIFIER | NA18966.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0177 | 1 | 338 | 0.0030 | 0 | c.868 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50817493 | G | A | intron_variant | MODIFIER | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0004others(1): Show | a0001c0001t0017a0001c0008t0017a0002c0004t0006others(4): Show | a0001c0001t0017g0266a0001c0008t0017g0042a0002c0004t0006g0032others(10): Show | 14 | 338 | 0.0414 | 0 | c.868 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50817596 | G | A | intron_variant | MODIFIER | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
a0002 | a0002c0004a0002c0006 | a0002c0004t0006a0002c0004t0044a0002c0006t0006 | a0002c0004t0006g0032a0002c0004t0006g0212a0002c0004t0006g0226others(5): Show | 9 | 338 | 0.0266 | 0 | c.868 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50818055 | C | T | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(111): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0020others(15): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(94): Show | 114 | 338 | 0.3373 | 0 | c.868 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50818191 | C | T | intron_variant | MODIFIER | HG02145.hp2 HG03486.hp1 |
a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0040a0001c0001t0016g0041 | 2 | 338 | 0.0059 | 0 | c.868 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50818220 | G | C | intron_variant | MODIFIER | HG03516.hp2 | a0001 | a0001c0007 | a0001c0007t0033 | a0001c0007t0033g0245 | 1 | 338 | 0.0030 | 0 | c.868 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50818352 | T | A | intron_variant | MODIFIER | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(109): Show |
a0001 | a0001c0001a0001c0007a0001c0011 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0113a0001c0001t0002g0001a0001c0001t0002g0007others(90): Show | 112 | 338 | 0.3314 | 0 | c.868 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50818440 | A | G | intron_variant | MODIFIER | HG03471.hp1 | a0001 | a0001c0001 | a0001c0001t0040 | a0001c0001t0040g0047 | 1 | 338 | 0.0030 | 0 | c.867 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50818518 | C | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(51): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(274): Show | 327 | 338 | 0.9675 | 0 | c.867 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50818612 | C | A | intron_variant | MODIFIER | NA18987.hp2 NA19058.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0139a0001c0001t0001g0216 | 2 | 338 | 0.0059 | 0 | c.867 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50818711 | G | T | intron_variant | MODIFIER | NA19030.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0225 | 1 | 338 | 0.0030 | 0 | c.867 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50818804 | C | T | intron_variant | MODIFIER | HG02735.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0263 | 1 | 338 | 0.0030 | 0 | c.867 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50818956 | C | G | intron_variant | MODIFIER | HG01069.hp2 HG03516.hp2 |
a0001 | a0001c0001a0001c0007 | a0001c0001t0028a0001c0007t0033 | a0001c0001t0028g0052a0001c0007t0033g0245 | 2 | 338 | 0.0059 | 0 | c.867 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50818978 | A | G | intron_variant | MODIFIER | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(74): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0007others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0140a0001c0001t0002g0051a0001c0001t0002g0162others(63): Show | 77 | 338 | 0.2278 | 0 | c.867 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50819061 | G | C | intron_variant | MODIFIER | HG01243.hp1 HG01981.hp2 HG02723.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0019a0001c0001t0041a0001c0002t0004 | a0001c0001t0019g0241a0001c0001t0019g0242a0001c0001t0041g0037others(1): Show | 4 | 338 | 0.0118 | 0 | c.867 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50819137 | T | A | intron_variant | MODIFIER | HG01981.hp2 HG03139.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0041a0001c0002t0004 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | 338 | 0.0059 | 0 | c.867 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50819158 | C | G | intron_variant | MODIFIER | HG01167.hp2 HG02109.hp2 HG03491.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0103a0001c0001t0001g0122a0001c0001t0001g0130others(1): Show | 4 | 338 | 0.0118 | 0 | c.867 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50819250 | G | A | intron_variant | MODIFIER | HG01981.hp2 HG03139.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0041a0001c0002t0004 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | 338 | 0.0059 | 0 | c.867 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50819291 | C | T | intron_variant | MODIFIER | HG03471.hp1 | a0001 | a0001c0001 | a0001c0001t0040 | a0001c0001t0040g0047 | 1 | 338 | 0.0030 | 0 | c.867 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50819292 | G | A | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(66): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0010 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(57): Show | 69 | 338 | 0.2041 | 0 | c.867 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50819457 | C | T | intron_variant | MODIFIER | HG01981.hp2 HG03139.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0041a0001c0002t0004 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | 338 | 0.0059 | 0 | c.867 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50819491 | C | T | intron_variant | MODIFIER | HG02559.hp2 HG03540.hp1 |
a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0095a0001c0001t0015g0096 | 2 | 338 | 0.0059 | 0 | c.867 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50819494 | T | A | intron_variant | MODIFIER | HG02145.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0006 | a0001c0001t0001g0029a0001c0001t0001g0210a0001c0001t0001g0213others(2): Show | 6 | 338 | 0.0178 | 0 | c.867 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50819551 | C | T | intron_variant | MODIFIER | HG01243.hp1 HG02723.hp2 |
a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0241a0001c0001t0019g0242 | 2 | 338 | 0.0059 | 0 | c.867 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50819566 | G | A | intron_variant | MODIFIER | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0006a0001c0001t0008g0098 | 4 | 338 | 0.0118 | 0 | c.867 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50819654 | A | G | intron_variant | MODIFIER | HG00140.hp2 HG03669.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0027 | a0001c0001t0001g0133a0001c0001t0027g0084 | 2 | 338 | 0.0059 | 0 | c.867 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50819781 | G | C | intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0008 | a0001c0008t0017 | a0001c0008t0017g0042 | 1 | 338 | 0.0030 | 0 | c.867 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50819835 | T | C | 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.867 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50819943 | C | A | 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.867 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50819990 | T | A | intron_variant | MODIFIER | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0037 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | 338 | 0.0148 | 0 | c.867 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50820208 | C | T | intron_variant | MODIFIER | NA19240.hp2 | a0002 | a0002c0006 | a0002c0006t0006 | a0002c0006t0006g0045 | 1 | 338 | 0.0030 | 0 | c.867 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50820453 | G | A | intron_variant | MODIFIER | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(2): Show |
a0001a0002 | a0001c0008a0002c0004a0002c0006 | a0001c0008t0001a0002c0004t0044a0002c0006t0006 | a0001c0008t0001g0039a0002c0004t0044g0049a0002c0006t0006g0044others(2): Show | 5 | 338 | 0.0148 | 0 | c.867 others(6): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 8/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50820692 | G | A | intron_variant | MODIFIER | NA19081.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0148 | 1 | 338 | 0.0030 | 0 | c.770 others(6): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50820797 | A | G | 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.770 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50820889 | G | A | intron_variant | MODIFIER | HG02148.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0104 | 1 | 338 | 0.0030 | 0 | c.770 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50820933 | T | C | intron_variant | MODIFIER | HG01981.hp2 HG03139.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0041a0001c0002t0004 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | 338 | 0.0059 | 0 | c.770 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50821359 | C | T | 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.770 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50821442 | A | G | intron_variant | MODIFIER | HG02976.hp1 | a0001 | a0001c0001 | a0001c0001t0039 | a0001c0001t0039g0038 | 1 | 338 | 0.0030 | 0 | c.770 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50821535 | A | C | intron_variant | MODIFIER | NA19079.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0176 | 1 | 338 | 0.0030 | 0 | c.770 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar |