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 | 50855510 | C | G | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(99): Show |
a0001 | a0001c0001a0001c0003a0001c0011 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0169others(78): Show | 102 | 338 | 0.3018 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50855671 | C | A | intron_variant | MODIFIER | HG01243.hp1 HG02723.hp2 |
a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0241a0001c0001t0019g0242 | 2 | 338 | 0.0059 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50855911 | C | G | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0008others(1): Show | a0001c0001t0008a0001c0001t0009a0001c0001t0015others(6): Show | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(12): Show | 18 | 338 | 0.0533 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50856273 | G | A | intron_variant | MODIFIER | HG01243.hp1 HG02723.hp2 |
a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0241a0001c0001t0019g0242 | 2 | 338 | 0.0059 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50856287 | A | C | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(100): Show |
a0001 | a0001c0001a0001c0003a0001c0011 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0169others(79): Show | 103 | 338 | 0.3047 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50856307 | C | T | intron_variant | MODIFIER | HG01981.hp2 HG03139.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0041a0001c0002t0004 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | 338 | 0.0059 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50856463 | C | T | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(114): Show | 134 | 338 | 0.3965 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50856509 | G | T | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | a0001c0001t0001g0003a0001c0001t0001g0020a0001c0001t0001g0021others(111): Show | 131 | 338 | 0.3876 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50856558 | T | C | intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0249 | 1 | 338 | 0.0030 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50856582 | A | G | intron_variant | MODIFIER | NA18977.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0108 | 1 | 338 | 0.0030 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50856722 | G | A | intron_variant | MODIFIER | HG01981.hp2 HG03139.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0041a0001c0002t0004 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | 338 | 0.0059 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50856823 | G | A | intron_variant | MODIFIER | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0037 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | 338 | 0.0148 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50856951 | C | T | intron_variant | MODIFIER | NA18986.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0099 | 1 | 338 | 0.0030 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50856976 | C | T | intron_variant | MODIFIER | HG02897.hp2 | a0001 | a0001c0008 | a0001c0008t0001 | a0001c0008t0001g0039 | 1 | 338 | 0.0030 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50857083 | T | C | intron_variant | MODIFIER | HG02683.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0143 | 1 | 338 | 0.0030 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50857162 | C | T | intron_variant | MODIFIER | HG02280.hp1 HG03654.hp1 HG03710.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0014others(1): Show | a0001c0001t0001g0020a0001c0001t0005g0277a0001c0001t0005g0278others(5): Show | 9 | 338 | 0.0266 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50857187 | C | T | intron_variant | MODIFIER | HG02083.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0064 | 1 | 338 | 0.0030 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50857237 | G | A | intron_variant | MODIFIER | HG03225.hp2 NA20905.hp2 |
a0001 | a0001c0002a0001c0012 | a0001c0002t0004a0001c0012t0034 | a0001c0002t0004g0087a0001c0012t0034g0154 | 2 | 338 | 0.0059 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50857646 | C | G | intron_variant | MODIFIER | HG01257.hp2 HG01258.hp2 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0016 | 2 | 338 | 0.0059 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50857778 | T | C | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp2 HG01981.hp2 others(17): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0008others(1): Show | a0001c0001t0008a0001c0001t0009a0001c0001t0015others(7): Show | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(14): Show | 20 | 338 | 0.0592 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50857815 | G | A | intron_variant | MODIFIER | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0006a0001c0001t0008g0098 | 4 | 338 | 0.0118 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50857975 | A | T | intron_variant | MODIFIER | HG00735.hp2 HG03225.hp1 NA19240.hp1 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0010 | 3 | 338 | 0.0089 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50857985 | C | T | intron_variant | MODIFIER | NA18948.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0286 | 1 | 338 | 0.0030 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50858603 | G | C | intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0223 | 1 | 338 | 0.0030 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50858615 | T | C | intron_variant | MODIFIER | HG02280.hp2 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0258 | 1 | 338 | 0.0030 | 0 | c.99+ others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50858935 | G | A | intron_variant | MODIFIER | HG00621.hp1 NA19011.hp1 NA19060.hp2 |
a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0019a0001c0002t0004g0105 | 3 | 338 | 0.0089 | 0 | c.99+ others(6): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50859031 | G | T | intron_variant | MODIFIER | HG03942.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0107 | 1 | 338 | 0.0030 | 0 | c.99+ others(6): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50859037 | C | T | intron_variant | MODIFIER | HG01123.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0115 | 1 | 338 | 0.0030 | 0 | c.99+ others(6): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50859049 | T | C | intron_variant | MODIFIER | NA18954.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0140 | 1 | 338 | 0.0030 | 0 | c.99+ others(6): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50859268 | A | G | intron_variant | MODIFIER | HG01069.hp2 HG02615.hp1 |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0028a0002c0004t0045 | a0001c0001t0028g0052a0002c0004t0045g0200 | 2 | 338 | 0.0059 | 0 | c.99+ others(6): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50859414 | C | T | intron_variant | MODIFIER | HG00741.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0265 | 1 | 338 | 0.0030 | 0 | c.99+ others(6): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50859464 | G | C | intron_variant | MODIFIER | HG01981.hp2 HG03139.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0041a0001c0002t0004 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | 338 | 0.0059 | 0 | c.99+ others(6): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50859527 | C | T | intron_variant | MODIFIER | HG03453.hp2 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0207 | 1 | 338 | 0.0030 | 0 | c.99+ others(6): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50859675 | T | C | intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0271 | 1 | 338 | 0.0030 | 0 | c.99+ others(6): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50859814 | A | G | intron_variant | MODIFIER | HG02258.hp2 HG03516.hp2 |
a0001 | a0001c0007 | a0001c0007t0005a0001c0007t0033 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | 338 | 0.0059 | 0 | c.99+ others(5): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50859911 | T | G | synonymous_variant | LOW | HG03225.hp2 | a0001 | a0001c0012 | a0001c0012t0034 | a0001c0012t0034g0154 | 1 | 338 | 0.0030 | 0 | c.30A others(2): Show |
p.Gly others(5): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 3/13 | 170/9221 | 30/1761 | 10/586 | chr10 | TogoVar | ||
A1CF_chr10_50794409_50890627 | 50860152 | A | G | intron_variant | MODIFIER | HG01257.hp1 | a0001 | a0001c0001 | a0001c0001t0021 | a0001c0001t0021g0110 | 1 | 338 | 0.0030 | 0 | c.-45 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50860196 | A | C | intron_variant | MODIFIER | HG03669.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0234 | 1 | 338 | 0.0030 | 0 | c.-45 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50860449 | G | C | intron_variant | MODIFIER | HG02132.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0089 | 1 | 338 | 0.0030 | 0 | c.-45 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50860683 | G | A | intron_variant | MODIFIER | HG04204.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0144 | 1 | 338 | 0.0030 | 0 | c.-45 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50860705 | G | A | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(48): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(265): Show | 318 | 338 | 0.9408 | 0 | c.-45 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50860930 | T | C | intron_variant | MODIFIER | HG01981.hp2 HG03139.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0041a0001c0002t0004 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | 338 | 0.0059 | 0 | c.-45 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50861038 | T | C | intron_variant | MODIFIER | HG02559.hp1 HG02717.hp1 HG03453.hp2 |
a0001 | a0001c0005 | a0001c0005t0001a0001c0005t0024a0001c0005t0048 | a0001c0005t0001g0207a0001c0005t0024g0208a0001c0005t0048g0209 | 3 | 338 | 0.0089 | 0 | c.-45 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50861051 | G | C | intron_variant | MODIFIER | HG01243.hp1 HG02723.hp2 |
a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0241a0001c0001t0019g0242 | 2 | 338 | 0.0059 | 0 | c.-45 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50861060 | G | A | intron_variant | MODIFIER | HG02922.hp2 | a0001 | a0001c0001 | a0001c0001t0037 | a0001c0001t0037g0050 | 1 | 338 | 0.0030 | 0 | c.-45 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50861440 | A | G | intron_variant | MODIFIER | HG03710.hp2 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0082 | 1 | 338 | 0.0030 | 0 | c.-45 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50861502 | G | C | intron_variant | MODIFIER | HG02922.hp2 | a0001 | a0001c0001 | a0001c0001t0037 | a0001c0001t0037g0050 | 1 | 338 | 0.0030 | 0 | c.-45 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50861513 | T | C | intron_variant | MODIFIER | HG02723.hp2 | a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0242 | 1 | 338 | 0.0030 | 0 | c.-45 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50861771 | A | G | intron_variant | MODIFIER | HG01361.hp2 | a0001 | a0001c0001 | a0001c0001t0023 | a0001c0001t0023g0114 | 1 | 338 | 0.0030 | 0 | c.-45 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50861784 | A | G | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0007others(2): Show | a0001c0001t0008a0001c0001t0009a0001c0001t0015others(8): Show | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(14): Show | 20 | 338 | 0.0592 | 0 | c.-45 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 2/12 | chr10 | TogoVar |