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 | 50824153 | G | A | intron_variant | MODIFIER | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0028a0002c0004t0044a0002c0004t0045 | a0001c0001t0028g0052a0002c0004t0044g0049a0002c0004t0045g0200 | 3 | 338 | 0.0089 | 0 | c.770 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50824284 | C | T | intron_variant | MODIFIER | HG00423.hp1 | a0001 | a0001c0001 | a0001c0001t0032 | a0001c0001t0032g0058 | 1 | 338 | 0.0030 | 0 | c.770 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50824285 | G | A | intron_variant | MODIFIER | HG02258.hp2 HG03516.hp2 |
a0001 | a0001c0007 | a0001c0007t0005a0001c0007t0033 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | 338 | 0.0059 | 0 | c.770 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50824350 | T | C | intron_variant | MODIFIER | HG00438.hp1 HG00639.hp1 HG00735.hp2 others(57): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(7): Show | a0001c0001t0001g0276a0001c0001t0003g0008a0001c0001t0003g0018others(46): Show | 60 | 338 | 0.1775 | 0 | c.770 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50824412 | G | T | intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0096 | 1 | 338 | 0.0030 | 0 | c.769 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50824709 | C | T | intron_variant | MODIFIER | NA19003.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0137 | 1 | 338 | 0.0030 | 0 | c.769 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50824917 | C | T | intron_variant | MODIFIER | HG02258.hp1 HG02922.hp2 HG03139.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0037 | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0037g0050 | 5 | 338 | 0.0148 | 0 | c.769 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50824949 | C | A | intron_variant | MODIFIER | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0006a0001c0001t0008g0098 | 4 | 338 | 0.0118 | 0 | c.769 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50825233 | C | T | intron_variant | MODIFIER | HG01978.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0121 | 1 | 338 | 0.0030 | 0 | c.769 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50825450 | T | A | intron_variant | MODIFIER | NA18945.hp2 NA19080.hp2 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0013 | 2 | 338 | 0.0059 | 0 | c.769 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50825453 | G | A | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0009a0001c0001t0043a0001c0002t0004 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(2): Show | 6 | 338 | 0.0178 | 0 | c.769 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50825479 | A | G | intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0223 | 1 | 338 | 0.0030 | 0 | c.769 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50826129 | T | C | intron_variant | MODIFIER | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
a0001a0002 | a0001c0008a0002c0006 | a0001c0008t0001a0002c0006t0006 | a0001c0008t0001g0039a0002c0006t0006g0044a0002c0006t0006g0045others(1): Show | 4 | 338 | 0.0118 | 0 | c.769 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50826428 | A | G | intron_variant | MODIFIER | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0028a0002c0004t0044a0002c0004t0045 | a0001c0001t0028g0052a0002c0004t0044g0049a0002c0004t0045g0200 | 3 | 338 | 0.0089 | 0 | c.769 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50826446 | G | A | intron_variant | MODIFIER | HG01981.hp2 HG03139.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0041a0001c0002t0004 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | 338 | 0.0059 | 0 | c.769 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50826480 | C | T | intron_variant | MODIFIER | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
a0001a0002 | a0001c0008a0002c0006 | a0001c0008t0001a0002c0006t0006 | a0001c0008t0001g0039a0002c0006t0006g0044a0002c0006t0006g0045others(1): Show | 4 | 338 | 0.0118 | 0 | c.769 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50826533 | G | 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.769 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50826560 | A | G | intron_variant | MODIFIER | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0028a0002c0004t0044a0002c0004t0045 | a0001c0001t0028g0052a0002c0004t0044g0049a0002c0004t0045g0200 | 3 | 338 | 0.0089 | 0 | c.769 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50826579 | T | G | intron_variant | MODIFIER | NA20129.hp1 | a0002 | a0002c0004 | a0002c0004t0044 | a0002c0004t0044g0049 | 1 | 338 | 0.0030 | 0 | c.769 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50826860 | T | C | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(49): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(276): Show | 330 | 338 | 0.9763 | 0 | c.769 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50826869 | C | T | intron_variant | MODIFIER | NA18955.hp1 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0078 | 1 | 338 | 0.0030 | 0 | c.769 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50826910 | T | C | intron_variant | MODIFIER | HG03704.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0264 | 1 | 338 | 0.0030 | 0 | c.769 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50827088 | C | A | intron_variant | MODIFIER | NA18964.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0185 | 1 | 338 | 0.0030 | 0 | c.769 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50827313 | A | G | intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0012 | a0001c0012t0034 | a0001c0012t0034g0154 | 1 | 338 | 0.0030 | 0 | c.769 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50827410 | G | T | intron_variant | MODIFIER | NA19060.hp2 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0105 | 1 | 338 | 0.0030 | 0 | c.769 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50827485 | C | A | intron_variant | MODIFIER | HG01069.hp2 HG01884.hp2 HG01891.hp2 others(21): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0007others(3): Show | a0001c0001t0008a0001c0001t0009a0001c0001t0015others(11): Show | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(18): Show | 24 | 338 | 0.0710 | 0 | c.769 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50827506 | A | T | intron_variant | MODIFIER | HG02074.hp2 NA19081.hp1 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0059a0001c0001t0003g0061 | 2 | 338 | 0.0059 | 0 | c.769 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50827812 | G | T | intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0012 | a0001c0012t0034 | a0001c0012t0034g0154 | 1 | 338 | 0.0030 | 0 | c.769 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50827870 | A | G | intron_variant | MODIFIER | HG02015.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0186 | 1 | 338 | 0.0030 | 0 | c.769 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50827932 | A | G | intron_variant | MODIFIER | HG01069.hp2 HG01884.hp2 HG01891.hp2 others(10): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0009a0001c0001t0015a0001c0001t0028others(5): Show | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(9): Show | 13 | 338 | 0.0385 | 0 | c.769 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50827955 | T | C | intron_variant | MODIFIER | HG01243.hp1 HG02723.hp2 |
a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0241a0001c0001t0019g0242 | 2 | 338 | 0.0059 | 0 | c.769 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50827989 | G | A | intron_variant | MODIFIER | HG00621.hp1 NA19011.hp1 NA19060.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0020a0001c0002t0004 | a0001c0001t0020g0112a0001c0002t0004g0019a0001c0002t0004g0105 | 4 | 338 | 0.0118 | 0 | c.769 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50828002 | A | G | intron_variant | MODIFIER | HG02132.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0175 | 1 | 338 | 0.0030 | 0 | c.769 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 7/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50828803 | G | C | intron_variant | MODIFIER | HG02258.hp2 HG03516.hp2 |
a0001 | a0001c0007 | a0001c0007t0005a0001c0007t0033 | a0001c0007t0005g0244a0001c0007t0033g0245 | 2 | 338 | 0.0059 | 0 | c.605 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50828813 | A | T | intron_variant | MODIFIER | HG02258.hp1 HG03139.hp1 HG06807.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0006a0001c0001t0008g0098 | 4 | 338 | 0.0118 | 0 | c.605 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50828907 | A | G | intron_variant | MODIFIER | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
a0001a0002 | a0001c0008a0002c0006 | a0001c0008t0001a0002c0006t0006 | a0001c0008t0001g0039a0002c0006t0006g0044a0002c0006t0006g0045others(1): Show | 4 | 338 | 0.0118 | 0 | c.605 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50828945 | A | C | intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0206 | 1 | 338 | 0.0030 | 0 | c.605 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50829091 | A | G | 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.605 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50829247 | G | T | intron_variant | MODIFIER | HG01981.hp2 HG03139.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0041a0001c0002t0004 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | 338 | 0.0059 | 0 | c.605 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50829268 | T | A | intron_variant | MODIFIER | HG01981.hp2 HG03139.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0041a0001c0002t0004 | a0001c0001t0041g0037a0001c0002t0004g0036 | 2 | 338 | 0.0059 | 0 | c.605 others(7): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50829345 | G | T | intron_variant | MODIFIER | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
a0001a0002 | a0001c0008a0002c0006 | a0001c0008t0001a0002c0006t0006 | a0001c0008t0001g0039a0002c0006t0006g0044a0002c0006t0006g0045others(1): Show | 4 | 338 | 0.0118 | 0 | c.605 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50829399 | G | A | intron_variant | MODIFIER | HG01069.hp2 HG02615.hp1 NA20129.hp1 |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0028a0002c0004t0044a0002c0004t0045 | a0001c0001t0028g0052a0002c0004t0044g0049a0002c0004t0045g0200 | 3 | 338 | 0.0089 | 0 | c.605 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50829666 | C | G | intron_variant | MODIFIER | NA18980.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0179 | 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 | 50829836 | G | A | intron_variant | MODIFIER | HG01069.hp2 HG01884.hp2 HG01891.hp2 others(21): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0007others(3): Show | a0001c0001t0008a0001c0001t0009a0001c0001t0015others(11): Show | a0001c0001t0008g0006a0001c0001t0008g0098a0001c0001t0009g0026others(18): Show | 24 | 338 | 0.0710 | 0 | c.605 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50829944 | C | G | intron_variant | MODIFIER | HG03710.hp1 | a0001 | a0001c0001 | a0001c0001t0038 | a0001c0001t0038g0168 | 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 | 50830224 | G | T | intron_variant | MODIFIER | HG03927.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0278 | 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 | 50830370 | G | A | intron_variant | MODIFIER | HG01884.hp2 HG02055.hp1 HG02572.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0009a0001c0002t0004 | a0001c0001t0009g0026a0001c0001t0009g0158a0001c0001t0009g0159others(1): Show | 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 | 50830485 | A | T | intron_variant | MODIFIER | HG02451.hp2 HG02897.hp2 NA18906.hp2 others(1): Show |
a0001a0002 | a0001c0008a0002c0006 | a0001c0008t0001a0002c0006t0006 | a0001c0008t0001g0039a0002c0006t0006g0044a0002c0006t0006g0045others(1): Show | 4 | 338 | 0.0118 | 0 | c.605 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar | ||||||
A1CF_chr10_50794409_50890627 | 50830685 | C | T | intron_variant | MODIFIER | HG01069.hp2 | a0001 | a0001c0001 | a0001c0001t0028 | a0001c0001t0028g0052 | 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 | 50830702 | T | C | intron_variant | MODIFIER | HG02083.hp2 NA18969.hp1 NA18983.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065 | 3 | 338 | 0.0089 | 0 | c.605 others(8): Show |
A1CF | ENSG00000148584.16 | transcript | ENST00000373997.8 | protein_coding | 6/12 | chr10 | TogoVar |