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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP30_chr1_161041946_161074891 | 161055801 | AAAT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
a0001a0002a0006others(2): Show | a0001c0001a0002c0002a0002c0003others(4): Show | a0001c0001t0001a0002c0002t0001a0002c0002t0004others(7): Show | a0001c0001t0001g0241a0001c0001t0001g0254a0001c0001t0001g0375others(142): Show | 151 | 390 | 0.3872 | -3 | c.345 others(18): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119354678 | ATTT | A | intron_variant | MODIFIER | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0007a0001c0001t0008a0001c0002t0004others(2): Show | a0001c0001t0007g0234a0001c0001t0007g0249a0001c0001t0007g0250others(15): Show | 18 | 310 | 0.0581 | -3 | c.101 others(22): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119357614 | AAAT | A | intron_variant | MODIFIER | HG00609.hp1 HG01943.hp2 HG02083.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0025others(6): Show | a0001c0001t0005g0168a0001c0001t0005g0169a0001c0001t0005g0172others(9): Show | 12 | 310 | 0.0387 | -3 | c.101 others(20): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119372280 | CTTT | C | intron_variant | MODIFIER | HG00408.hp2 HG00609.hp2 HG00639.hp2 others(31): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0006a0001c0001t0007a0001c0001t0008others(10): Show | a0001c0001t0006g0127a0001c0001t0007g0234a0001c0001t0007g0249others(30): Show | 34 | 310 | 0.1097 | -3 | c.348 others(20): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119376758 | CAAA | C | intron_variant | MODIFIER | HG01099.hp1 HG02257.hp1 HG02280.hp1 others(11): Show |
a0001a0003a0004others(1): Show | a0001c0002a0001c0005a0003c0006others(2): Show | a0001c0002t0012a0001c0005t0001a0001c0005t0057others(5): Show | a0001c0002t0012g0174a0001c0005t0001g0029a0001c0005t0001g0034others(11): Show | 14 | 310 | 0.0452 | -3 | c.349 others(20): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119390456 | CATT | C | intron_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(59): Show |
a0001a0002a0004others(5): Show | a0001c0001a0001c0002a0001c0004others(8): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(22): Show | a0001c0001t0005g0121a0001c0001t0005g0129a0001c0001t0006g0025others(58): Show | 62 | 310 | 0.2000 | -3 | c.683 others(18): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119412402 | AAAG | A | intron_variant | MODIFIER | HG00323.hp1 HG01099.hp2 HG01167.hp2 others(3): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0006a0001c0001t0008a0001c0004t0059 | a0001c0001t0006g0027a0001c0001t0006g0100a0001c0001t0006g0148others(3): Show | 6 | 310 | 0.0194 | -3 | c.192 others(22): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119424496 | TTTC | T | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(37): Show |
a0001a0011 | a0001c0001a0011c0019 | a0001c0001t0005a0001c0001t0007a0001c0001t0011others(3): Show | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(36): Show | 40 | 310 | 0.1290 | -3 | c.*82 others(14): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3783 | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119424505 | CTTT | C | downstream_gene_variant | MODIFIER | HG00609.hp2 HG02129.hp1 NA18940.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0007a0001c0001t0011 | a0001c0001t0005g0129a0001c0001t0005g0169a0001c0001t0007g0228others(3): Show | 6 | 310 | 0.0194 | -3 | c.*82 others(14): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3792 | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119424672 | ATTT | A | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00741.hp2 HG01167.hp1 others(31): Show |
a0001a0014 | a0001c0002a0001c0004a0014c0014 | a0001c0002t0003a0001c0004t0003a0001c0004t0010others(5): Show | a0001c0002t0003g0143a0001c0002t0003g0144a0001c0004t0003g0007others(30): Show | 34 | 310 | 0.1097 | -3 | c.*84 others(14): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 3959 | chr3 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128977851 | TTTA | T | intron_variant | MODIFIER | HG00280.hp1 HG00423.hp1 HG00741.hp2 others(56): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(16): Show | a0001c0001t0001g0009a0001c0001t0001g0020a0001c0001t0001g0027others(56): Show | 59 | 398 | 0.1482 | -3 | c.212 others(20): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 19/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128979881 | GTTA | G | intron_variant | MODIFIER | HG02809.hp2 HG03209.hp1 HG03540.hp1 |
a0005 | a0005c0011 | a0005c0011t0008a0005c0011t0021 | a0005c0011t0008g0072a0005c0011t0008g0073a0005c0011t0021g0071 | 3 | 398 | 0.0075 | -3 | c.197 others(20): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 18/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128987987 | TAAG | T | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
a0001a0003a0005others(3): Show | a0001c0001a0001c0010a0001c0014others(9): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0022others(17): Show | a0001c0001t0002g0002a0001c0001t0002g0041a0001c0001t0002g0094others(106): Show | 110 | 398 | 0.2764 | -3 | c.129 others(18): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 13/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129028744 | AGAG | A | intron_variant | MODIFIER | HG02280.hp1 HG03139.hp1 HG03831.hp2 others(1): Show |
a0001 | a0001c0001a0001c0010 | a0001c0001t0016a0001c0001t0033a0001c0010t0014 | a0001c0001t0016g0196a0001c0001t0016g0197a0001c0001t0033g0299others(1): Show | 4 | 398 | 0.0101 | -3 | c.104 others(24): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 11/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129051953 | CAAA | C | intron_variant | MODIFIER | HG00280.hp1 HG00642.hp2 HG01069.hp2 others(38): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(14): Show | a0001c0001t0001g0013a0001c0001t0001g0056a0001c0001t0002g0109others(38): Show | 41 | 398 | 0.1030 | -3 | c.963 others(22): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 10/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129067618 | GCAA | G | intron_variant | MODIFIER | HG01496.hp2 HG02451.hp1 HG02451.hp2 others(7): Show |
a0001a0004a0005others(1): Show | a0001c0010a0001c0015a0001c0016others(3): Show | a0001c0010t0008a0001c0015t0035a0001c0016t0002others(5): Show | a0001c0010t0008g0191a0001c0010t0008g0192a0001c0015t0035g0095others(7): Show | 10 | 398 | 0.0251 | -3 | c.532 others(18): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 6/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129073782 | CAAA | C | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp2 HG01258.hp2 others(32): Show |
a0001a0002a0007others(1): Show | a0001c0001a0001c0014a0002c0008others(3): Show | a0001c0001t0002a0001c0001t0004a0001c0014t0004others(4): Show | a0001c0001t0002g0156a0001c0001t0002g0158a0001c0001t0002g0166others(32): Show | 35 | 398 | 0.0879 | -3 | c.532 others(20): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 6/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129086820 | CAAA | C | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp2 HG01258.hp2 others(32): Show |
a0001a0002a0007others(1): Show | a0001c0001a0001c0014a0002c0007others(4): Show | a0001c0001t0002a0001c0001t0004a0001c0014t0004others(5): Show | a0001c0001t0002g0156a0001c0001t0002g0158a0001c0001t0002g0166others(32): Show | 35 | 398 | 0.0879 | -3 | c.531 others(20): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 6/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129088995 | CAAA | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(209): Show |
a0001a0002a0003others(13): Show | a0001c0001a0001c0002a0001c0003others(28): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(49): Show | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0350others(209): Show | 212 | 398 | 0.5327 | -3 | c.531 others(20): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 6/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129127769 | TAAC | T | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(59): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0034others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0022others(4): Show | a0001c0001t0002g0002a0001c0001t0002g0094a0001c0001t0002g0096others(58): Show | 62 | 398 | 0.1558 | -3 | c.226 others(20): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129138313 | AAAG | A | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(98): Show |
a0001a0002a0007others(2): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0016others(16): Show | a0001c0001t0002g0002a0001c0001t0002g0094a0001c0001t0002g0098others(97): Show | 101 | 398 | 0.2538 | -3 | c.226 others(22): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129193308 | TGGG | T | upstream_gene_variant | MODIFIER | HG00140.hp2 HG00597.hp1 HG00639.hp1 others(24): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0002t0001others(4): Show | a0001c0001t0002g0107a0001c0001t0002g0114a0001c0001t0002g0122others(24): Show | 27 | 398 | 0.0678 | -3 | c.-11 others(14): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 984 | chr11 | TogoVar | ||||||
ARHGAP33_chr19_35770564_35793822 | 35771989 | CTTT | C | upstream_gene_variant | MODIFIER | HG00408.hp2 HG00621.hp1 HG00733.hp1 others(68): Show |
a0001 | a0001c0003a0001c0007a0001c0012others(2): Show | a0001c0003t0001a0001c0007t0001a0001c0012t0001others(2): Show | a0001c0003t0001g0006a0001c0003t0001g0009a0001c0003t0001g0011others(16): Show | 71 | 420 | 0.1691 | -3 | c.-36 others(14): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3574 | chr19 | TogoVar | ||||||
ARHGAP33_chr19_35770564_35793822 | 35773965 | CTTT | C | upstream_gene_variant | MODIFIER | HG00423.hp1 HG00558.hp2 HG00673.hp1 others(15): Show |
a0001 | a0001c0002a0001c0004a0001c0006others(2): Show | a0001c0002t0001a0001c0004t0001a0001c0006t0001others(2): Show | a0001c0002t0001g0018a0001c0004t0001g0008a0001c0004t0001g0010others(6): Show | 18 | 420 | 0.0429 | -3 | c.-16 others(14): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1598 | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46886781 | CTTA | C | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(79): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(2): Show | a0001c0001t0001g0130a0001c0001t0001g0134a0001c0001t0001g0142others(79): Show | 82 | 298 | 0.2752 | -3 | c.-18 others(24): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46899628 | AGGT | A | intron_variant | MODIFIER | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(1): Show | 4 | 298 | 0.0134 | -3 | c.-18 others(24): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46908482 | TTTG | T | intron_variant | MODIFIER | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
a0001 | a0001c0002a0001c0005a0001c0006 | a0001c0002t0006a0001c0002t0036a0001c0005t0006others(1): Show | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | 298 | 0.0470 | -3 | c.-18 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46914446 | AAAT | A | intron_variant | MODIFIER | HG02886.hp2 HG03130.hp2 HG03195.hp1 others(2): Show |
a0001a0004 | a0001c0001a0004c0008 | a0001c0001t0015a0001c0001t0023a0001c0001t0041others(1): Show | a0001c0001t0015g0037a0001c0001t0023g0039a0001c0001t0023g0055others(2): Show | 5 | 298 | 0.0168 | -3 | c.-18 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46978607 | TGTG | T | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(46): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0009others(5): Show | a0001c0001t0001g0142a0001c0001t0001g0170a0001c0001t0001g0172others(46): Show | 49 | 298 | 0.1644 | -3 | c.382 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 47006267 | CTTT | C | downstream_gene_variant | MODIFIER | HG00408.hp1 HG00558.hp1 NA18951.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0005a0001c0001t0039 | a0001c0001t0004g0022a0001c0001t0004g0072a0001c0001t0004g0237others(5): Show | 8 | 298 | 0.0269 | -3 | c.*55 others(14): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1191 | chr19 | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131080398 | TAAA | T | intron_variant | MODIFIER | HG01069.hp1 HG02809.hp2 HG02897.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006 | a0001c0001t0001g0189a0001c0001t0001g0202a0001c0001t0002g0229others(1): Show | 4 | 302 | 0.0133 | -3 | c.-14 others(22): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ARHGAP39_chr8_144524179_144690846 | 144525287 | TCTC | T | downstream_gene_variant | MODIFIER | HG02055.hp2 HG02809.hp2 HG02976.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0150a0001c0001t0004g0152a0001c0001t0004g0154others(4): Show | 7 | 246 | 0.0285 | -3 | c.*51 others(14): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3891 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144528689 | GCCC | G | downstream_gene_variant | MODIFIER | HG02055.hp2 HG02258.hp1 HG02809.hp2 others(18): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0004a0001c0001t0016others(4): Show | a0001c0001t0001g0024a0001c0001t0001g0047a0001c0001t0001g0220others(18): Show | 21 | 246 | 0.0854 | -3 | c.*17 others(14): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 489 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144535795 | TGAA | T | intron_variant | MODIFIER | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
a0001 | a0001c0001a0001c0007a0001c0018 | a0001c0001t0001a0001c0007t0001a0001c0018t0001 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(8): Show | 11 | 246 | 0.0447 | -3 | c.261 others(22): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144559354 | CAAA | C | intron_variant | MODIFIER | HG00558.hp2 HG00639.hp1 HG01168.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0005a0002c0008 | a0001c0001t0001a0001c0001t0005a0001c0001t0020others(2): Show | a0001c0001t0001g0236a0001c0001t0005g0187a0001c0001t0020g0079others(2): Show | 5 | 246 | 0.0203 | -3 | c.513 others(20): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144576332 | CAAA | C | intron_variant | MODIFIER | HG02572.hp2 HG02809.hp2 HG02886.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0017 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(3): Show | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0003g0023others(9): Show | 12 | 246 | 0.0488 | -3 | c.512 others(20): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144600975 | TGGA | T | intron_variant | MODIFIER | HG02280.hp1 HG02451.hp2 HG02622.hp1 others(5): Show |
a0001a0005 | a0001c0001a0001c0004a0001c0007others(1): Show | a0001c0001t0007a0001c0004t0006a0001c0007t0001others(1): Show | a0001c0001t0007g0018a0001c0004t0006g0069a0001c0004t0006g0070others(5): Show | 8 | 246 | 0.0325 | -3 | c.80+ others(18): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144601583 | TGGA | T | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0009others(4): Show | a0001c0001t0001g0236a0001c0003t0001g0005a0001c0003t0001g0012others(9): Show | 12 | 246 | 0.0488 | -3 | c.80+ others(18): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144602240 | TGGA | T | intron_variant | MODIFIER | HG00639.hp2 NA18941.hp1 NA21309.hp1 |
a0001 | a0001c0001a0001c0002a0001c0017 | a0001c0001t0001a0001c0002t0001a0001c0017t0001 | a0001c0001t0001g0177a0001c0002t0001g0088a0001c0017t0001g0064 | 3 | 246 | 0.0122 | -3 | c.80+ others(18): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144602703 | TGGA | T | intron_variant | MODIFIER | HG02257.hp1 HG02258.hp1 HG03209.hp1 others(1): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0003a0001c0001t0018a0001c0001t0021others(1): Show | a0001c0001t0003g0023a0001c0001t0018g0022a0001c0001t0021g0062others(1): Show | 4 | 246 | 0.0163 | -3 | c.80+ others(18): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144682548 | CAAA | C | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG02004.hp1 others(30): Show |
a0001 | a0001c0001a0001c0002a0001c0014 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(7): Show | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(30): Show | 33 | 246 | 0.1342 | -3 | c.-82 others(20): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38635366 | ATAT | A | intron_variant | MODIFIER | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
a0001a0004a0021others(1): Show | a0001c0002a0001c0008a0004c0011others(3): Show | a0001c0002t0004a0001c0008t0004a0004c0011t0004others(4): Show | a0001c0002t0004g0073a0001c0008t0004g0026a0001c0008t0004g0309others(7): Show | 12 | 350 | 0.0343 | -3 | c.949 others(18): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38640101 | TTCC | T | intron_variant | MODIFIER | HG01261.hp1 HG01884.hp1 HG01884.hp2 others(13): Show |
a0001a0007a0008others(2): Show | a0001c0002a0001c0007a0007c0040others(4): Show | a0001c0002t0008a0001c0002t0010a0001c0007t0001others(6): Show | a0001c0002t0008g0074a0001c0002t0010g0082a0001c0007t0001g0189others(12): Show | 16 | 350 | 0.0457 | -3 | c.127 others(20): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38648505 | ATGC | A | intron_variant | MODIFIER | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
a0008a0022 | a0008c0013a0008c0017a0022c0023 | a0008c0013t0008a0008c0017t0008a0022c0023t0011 | a0008c0013t0008g0028a0008c0013t0008g0303a0008c0017t0008g0046others(2): Show | 6 | 350 | 0.0171 | -3 | c.188 others(20): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38653148 | GATA | G | downstream_gene_variant | MODIFIER | HG00642.hp2 HG01516.hp2 HG01517.hp1 others(29): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0002a0001c0004others(8): Show | a0001c0001t0005a0001c0002t0004a0001c0004t0004others(10): Show | a0001c0001t0005g0187a0001c0001t0005g0255a0001c0002t0004g0073others(25): Show | 32 | 350 | 0.0914 | -3 | c.*33 others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2496 | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38653151 | AATG | A | downstream_gene_variant | MODIFIER | HG01109.hp1 HG02559.hp2 HG02896.hp2 others(3): Show |
a0001a0007 | a0001c0002a0007c0010 | a0001c0002t0008a0001c0002t0010a0007c0010t0010others(1): Show | a0001c0002t0008g0074a0001c0002t0010g0082a0007c0010t0010g0224others(3): Show | 6 | 350 | 0.0171 | -3 | c.*33 others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2499 | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38653371 | ATGG | A | downstream_gene_variant | MODIFIER | HG01192.hp2 HG01515.hp1 HG01517.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0170a0001c0001t0002g0061a0001c0001t0002g0109others(1): Show | 4 | 350 | 0.0114 | -3 | c.*35 others(14): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 2719 | chr20 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100690262 | GTTA | G | intron_variant | MODIFIER | HG00597.hp2 HG00673.hp2 HG01070.hp1 others(27): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0015others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(5): Show | a0001c0001t0001g0266a0001c0001t0001g0271a0001c0001t0001g0275others(27): Show | 30 | 286 | 0.1049 | -3 | c.154 others(20): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100700406 | CTCT | C | intron_variant | MODIFIER | HG00597.hp2 HG00673.hp2 HG01070.hp1 others(27): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0015others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(5): Show | a0001c0001t0001g0266a0001c0001t0001g0271a0001c0001t0001g0275others(27): Show | 30 | 286 | 0.1049 | -3 | c.154 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100702952 | GTAA | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(184): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0008others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(44): Show | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0023others(184): Show | 187 | 286 | 0.6539 | -3 | c.154 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |