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 | 50810463 | G | A | intron_variant | MODIFIER | HG02683.hp2 HG04204.hp2 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0143a0001c0001t0005g0144 | 2 | 338 | 0.0059 | 0 | c.146 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50810481 | G | T | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0020others(15): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(95): Show | 115 | 338 | 0.3402 | 0 | c.146 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50810503 | A | G | intron_variant | MODIFIER | HG01069.hp2 HG03516.hp2 |
a0001 | a0001c0001a0001c0007 | a0001c0001t0028a0001c0007t0033 | a0001c0001t0028g0052a0001c0007t0033g0245 | 2 | 338 | 0.0059 | 0 | c.146 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50810578 | G | A | intron_variant | MODIFIER | HG03516.hp2 | a0001 | a0001c0007 | a0001c0007t0033 | a0001c0007t0033g0245 | 1 | 338 | 0.0030 | 0 | c.146 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50810620 | G | A | intron_variant | MODIFIER | HG02055.hp1 NA18945.hp1 NA18987.hp1 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0004a0001c0003t0001 | a0001c0002t0004g0160a0001c0003t0001g0109a0001c0003t0001g0222 | 3 | 338 | 0.0089 | 0 | c.146 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50810881 | C | T | intron_variant | MODIFIER | HG01243.hp1 HG02723.hp2 |
a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0241a0001c0001t0019g0242 | 2 | 338 | 0.0059 | 0 | c.146 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50810983 | T | G | intron_variant | MODIFIER | HG00639.hp1 HG02055.hp2 HG02145.hp1 others(5): Show |
a0002 | a0002c0004a0002c0006 | a0002c0004t0006a0002c0006t0006 | a0002c0004t0006g0032a0002c0004t0006g0212a0002c0004t0006g0226others(4): Show | 8 | 338 | 0.0237 | 0 | c.146 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 11/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50811287 | C | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(55): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(283): Show | 337 | 338 | 0.9970 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50811298 | A | G | intron_variant | MODIFIER | HG00673.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0135 | 1 | 338 | 0.0030 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50811304 | T | A | intron_variant | MODIFIER | HG00738.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0149 | 1 | 338 | 0.0030 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50811405 | T | C | intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0271 | 1 | 338 | 0.0030 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50811485 | A | G | 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.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50811532 | C | T | intron_variant | MODIFIER | HG02886.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0205 | 1 | 338 | 0.0030 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50811600 | C | T | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp2 HG02559.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0009a0001c0001t0015a0001c0001t0043 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(3): Show | 7 | 338 | 0.0207 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50811613 | A | T | intron_variant | MODIFIER | HG01167.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0130 | 1 | 338 | 0.0030 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50811668 | G | C | intron_variant | MODIFIER | NA20129.hp1 | a0002 | a0002c0004 | a0002c0004t0044 | a0002c0004t0044g0049 | 1 | 338 | 0.0030 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50811742 | C | G | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(51): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(255): Show | 303 | 338 | 0.8965 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50811909 | T | G | intron_variant | MODIFIER | HG01981.hp2 | a0001 | a0001c0001 | a0001c0001t0041 | a0001c0001t0041g0037 | 1 | 338 | 0.0030 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50811941 | A | G | intron_variant | MODIFIER | HG03491.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0131 | 1 | 338 | 0.0030 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50811954 | G | A | intron_variant | MODIFIER | NA19070.hp1 | a0001 | a0001c0003 | a0001c0003t0007 | a0001c0003t0007g0232 | 1 | 338 | 0.0030 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50811969 | T | C | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp2 HG02559.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0009a0001c0001t0015a0001c0001t0043 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(3): Show | 7 | 338 | 0.0207 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50812043 | A | G | intron_variant | MODIFIER | HG01943.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0236 | 1 | 338 | 0.0030 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50812164 | T | C | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(106): Show |
a0001 | a0001c0001a0001c0011 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0113a0001c0001t0002g0001a0001c0001t0002g0007others(87): Show | 109 | 338 | 0.3225 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50812251 | G | A | intron_variant | MODIFIER | HG00423.hp1 | a0001 | a0001c0001 | a0001c0001t0032 | a0001c0001t0032g0058 | 1 | 338 | 0.0030 | 0 | c.132 others(9): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50812341 | C | T | intron_variant | MODIFIER | HG02735.hp1 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0081 | 1 | 338 | 0.0030 | 0 | c.132 others(9): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50812359 | G | A | intron_variant | MODIFIER | NA19090.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0183 | 1 | 338 | 0.0030 | 0 | c.132 others(9): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50812526 | C | T | intron_variant | MODIFIER | HG01981.hp2 HG02257.hp1 HG02922.hp2 others(3): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0017a0001c0001t0037a0001c0001t0039others(3): Show | a0001c0001t0017g0266a0001c0001t0037g0050a0001c0001t0039g0038others(3): Show | 6 | 338 | 0.0178 | 0 | c.132 others(9): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50812613 | T | C | intron_variant | MODIFIER | HG01891.hp2 | a0001 | a0001c0001 | a0001c0001t0043 | a0001c0001t0043g0094 | 1 | 338 | 0.0030 | 0 | c.132 others(9): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50812749 | C | T | intron_variant | MODIFIER | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(34): Show |
a0001 | a0001c0002a0001c0009 | a0001c0002t0004a0001c0002t0013a0001c0009t0004 | a0001c0002t0004g0002a0001c0002t0004g0019a0001c0002t0004g0036others(29): Show | 37 | 338 | 0.1095 | 0 | c.132 others(9): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50812880 | T | A | intron_variant | MODIFIER | HG02257.hp1 HG03471.hp1 HG04184.hp1 others(1): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0001a0001c0001t0017a0001c0001t0040others(1): Show | a0001c0001t0001g0090a0001c0001t0017g0266a0001c0001t0040g0047others(1): Show | 4 | 338 | 0.0118 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50812893 | G | 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.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50812964 | A | C | intron_variant | MODIFIER | HG02451.hp1 HG02572.hp2 |
a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0075a0001c0001t0012g0223 | 2 | 338 | 0.0059 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50812976 | C | T | intron_variant | MODIFIER | HG02886.hp2 HG03540.hp2 |
a0002 | a0002c0004 | a0002c0004t0018 | a0002c0004t0018g0034a0002c0004t0018g0153 | 2 | 338 | 0.0059 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50812981 | A | G | intron_variant | MODIFIER | HG02886.hp2 HG03540.hp2 |
a0002 | a0002c0004 | a0002c0004t0018 | a0002c0004t0018g0034a0002c0004t0018g0153 | 2 | 338 | 0.0059 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50813273 | A | C | intron_variant | MODIFIER | NA18947.hp2 NA18962.hp1 NA18986.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0024a0001c0001t0001g0099a0001c0001t0001g0147others(2): Show | 6 | 338 | 0.0178 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50813499 | C | A | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0009a0001c0001t0015a0001c0001t0016others(1): Show | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(5): Show | 9 | 338 | 0.0266 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50813654 | A | T | intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0012 | a0001c0012t0034 | a0001c0012t0034g0154 | 1 | 338 | 0.0030 | 0 | c.132 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 10/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50814086 | A | G | intron_variant | MODIFIER | HG03041.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0272 | 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 | 50814156 | T | C | intron_variant | MODIFIER | HG02148.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0215 | 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 | 50814208 | C | T | intron_variant | MODIFIER | HG01884.hp2 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0158 | 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 | 50814276 | C | T | intron_variant | MODIFIER | NA19003.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0137 | 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 | 50814313 | C | G | 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.114 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50814344 | A | G | intron_variant | MODIFIER | HG00438.hp2 HG00558.hp1 HG02027.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0049 | a0001c0001t0002g0170a0001c0001t0002g0172a0001c0001t0002g0175others(10): Show | 13 | 338 | 0.0385 | 0 | c.114 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50814707 | A | G | intron_variant | MODIFIER | HG00423.hp1 | a0001 | a0001c0001 | a0001c0001t0032 | a0001c0001t0032g0058 | 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 | 50814885 | A | G | intron_variant | MODIFIER | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(61): Show |
a0001 | a0001c0001a0001c0011 | a0001c0001t0002a0001c0001t0003a0001c0001t0030others(4): Show | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0027others(50): Show | 64 | 338 | 0.1894 | 0 | c.114 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50815113 | G | T | intron_variant | MODIFIER | HG03688.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0270 | 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 | 50815133 | C | T | intron_variant | MODIFIER | HG02257.hp1 HG03471.hp1 NA18906.hp1 |
a0001 | a0001c0001a0001c0008 | a0001c0001t0017a0001c0001t0040a0001c0008t0017 | a0001c0001t0017g0266a0001c0001t0040g0047a0001c0008t0017g0042 | 3 | 338 | 0.0089 | 0 | c.114 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50815394 | T | C | intron_variant | MODIFIER | HG02683.hp2 HG04204.hp2 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0143a0001c0001t0005g0144 | 2 | 338 | 0.0059 | 0 | c.114 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50815521 | T | A | intron_variant | MODIFIER | HG01071.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0128 | 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 | 50815728 | T | C | intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0012 | a0001c0012t0034 | a0001c0012t0034g0154 | 1 | 338 | 0.0030 | 0 | c.114 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 9/12 | chr10 | TogoVar |