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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP35_chr19_46855997_47010077 | 46939372 | CATTT | C | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(49): Show |
a0001a0003a0004 | a0001c0001a0001c0003a0003c0013others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0204a0001c0001t0002g0147a0001c0001t0002g0148others(49): Show | 52 | 298 | 0.1745 | -4 | c.382 others(23): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46952277 | CATTT | C | intron_variant | MODIFIER | HG03041.hp2 HG03471.hp2 HG03486.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0025 | a0001c0001t0001g0068a0001c0001t0003g0231a0001c0001t0025g0067 | 3 | 298 | 0.0101 | -4 | c.382 others(25): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46961966 | GAGAA | G | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0019a0001c0001t0029a0001c0001t0042 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | 298 | 0.0134 | -4 | c.382 others(25): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46965466 | TTTTG | T | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(111): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(33): Show | a0001c0001t0001g0068a0001c0001t0001g0204a0001c0001t0002g0267others(111): Show | 114 | 298 | 0.3826 | -4 | c.382 others(25): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46981408 | TAAGC | T | intron_variant | MODIFIER | HG02559.hp1 HG03139.hp1 HG03209.hp2 |
a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0087a0001c0001t0014g0247a0001c0001t0014g0248 | 3 | 298 | 0.0101 | -4 | c.382 others(23): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 47003914 | ACACG | A | 3_prime_UTR_variant | MODIFIER | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(31): Show |
a0001a0003a0006 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0004a0001c0001t0032a0001c0001t0039others(5): Show | a0001c0001t0004g0022a0001c0001t0004g0030a0001c0001t0004g0070others(31): Show | 34 | 298 | 0.1141 | -4 | c.*32 others(15): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||
ARHGAP36_chrX_131053346_131094885 | 131065041 | TTGTG | T | intron_variant | MODIFIER | HG00597.hp2 HG00642.hp1 HG01261.hp1 others(24): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0152a0001c0001t0001g0154a0001c0001t0001g0155others(22): Show | 27 | 302 | 0.0894 | -4 | c.-14 others(23): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ARHGAP36_chrX_131053346_131094885 | 131073855 | TAGAC | T | intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0154 | 1 | 302 | 0.0033 | -4 | c.-14 others(23): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ARHGAP36_chrX_131053346_131094885 | 131074356 | TGTGA | T | intron_variant | MODIFIER | HG01123.hp1 HG02486.hp1 HG02622.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0057a0001c0001t0001g0154a0001c0001t0002g0109others(8): Show | 12 | 302 | 0.0397 | -4 | c.-14 others(23): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ARHGAP36_chrX_131053346_131094885 | 131077764 | CATAT | C | intron_variant | MODIFIER | HG01168.hp2 HG01169.hp2 HG01516.hp1 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0035a0001c0001t0001g0130a0001c0001t0001g0131others(10): Show | 16 | 302 | 0.0530 | -4 | c.-14 others(23): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ARHGAP39_chr8_144524179_144690846 | 144528617 | GCCCA | G | downstream_gene_variant | MODIFIER | HG01891.hp1 HG01975.hp2 HG02055.hp2 others(55): Show |
a0001a0005 | a0001c0001a0001c0004a0001c0007others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0024a0001c0001t0001g0223a0001c0001t0001g0224others(55): Show | 58 | 246 | 0.2358 | -4 | c.*18 others(15): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 561 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144528689 | GCCCC | G | downstream_gene_variant | MODIFIER | HG01891.hp1 HG01975.hp2 HG02109.hp2 others(17): Show |
a0001a0005 | a0001c0001a0001c0007a0001c0012others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0020others(3): Show | a0001c0001t0002g0123a0001c0001t0002g0131a0001c0001t0002g0134others(17): Show | 20 | 246 | 0.0813 | -4 | c.*17 others(15): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 489 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144535814 | GTCTC | G | intron_variant | MODIFIER | HG02451.hp2 HG02572.hp1 HG03195.hp1 others(1): Show |
a0001 | a0001c0001a0001c0014 | a0001c0001t0007a0001c0014t0007 | a0001c0001t0007g0018a0001c0001t0007g0168a0001c0001t0007g0239others(1): Show | 4 | 246 | 0.0163 | -4 | c.261 others(23): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144575494 | CACAA | C | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(40): Show |
a0001a0004a0005 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(16): Show | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0001g0223others(40): Show | 43 | 246 | 0.1748 | -4 | c.512 others(21): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144576315 | AGAGT | A | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(9): Show |
a0001a0004a0005 | a0001c0003a0001c0005a0001c0007others(3): Show | a0001c0003t0001a0001c0003t0009a0001c0005t0001others(5): Show | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0110others(9): Show | 12 | 246 | 0.0488 | -4 | c.512 others(21): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144576332 | CAAAA | C | intron_variant | MODIFIER | HG02280.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
a0001 | a0001c0001a0001c0007a0001c0014 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(3): Show | a0001c0001t0001g0228a0001c0001t0004g0152a0001c0001t0004g0237others(5): Show | 8 | 246 | 0.0325 | -4 | c.512 others(21): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144579201 | CAAAA | C | intron_variant | MODIFIER | HG02055.hp2 HG02145.hp1 HG02572.hp2 others(11): Show |
a0001 | a0001c0001a0001c0002a0001c0017 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(2): Show | a0001c0001t0001g0024a0001c0001t0001g0151a0001c0001t0004g0150others(11): Show | 14 | 246 | 0.0569 | -4 | c.512 others(21): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144594546 | TAGTC | T | intron_variant | MODIFIER | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(9): Show |
a0001 | a0001c0001a0001c0018 | a0001c0001t0001a0001c0001t0002a0001c0018t0001 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(9): Show | 12 | 246 | 0.0488 | -4 | c.80+ others(21): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144602149 | CTGTG | C | intron_variant | MODIFIER | HG02109.hp1 HG02559.hp2 HG02622.hp2 others(7): Show |
a0001 | a0001c0001a0001c0018 | a0001c0001t0001a0001c0018t0001 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(7): Show | 10 | 246 | 0.0407 | -4 | c.80+ others(19): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144602880 | GGTGT | G | intron_variant | MODIFIER | HG00558.hp1 HG03041.hp1 NA18997.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0024a0001c0001t0001g0057a0001c0001t0001g0058others(3): Show | 6 | 246 | 0.0244 | -4 | c.80+ others(19): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144607235 | CAAAA | C | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(7): Show |
a0001a0004 | a0001c0003a0001c0005a0004c0009 | a0001c0003t0001a0001c0003t0009a0001c0005t0001others(2): Show | a0001c0003t0001g0005a0001c0003t0001g0012a0001c0003t0001g0014others(7): Show | 10 | 246 | 0.0407 | -4 | c.-81 others(21): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144639325 | CAAAA | C | intron_variant | MODIFIER | HG02109.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
a0001 | a0001c0001a0001c0018 | a0001c0001t0001a0001c0018t0001 | a0001c0001t0001g0229a0001c0001t0001g0231a0001c0001t0001g0232others(2): Show | 5 | 246 | 0.0203 | -4 | c.-81 others(23): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144639338 | AAAAG | A | intron_variant | MODIFIER | HG02055.hp2 HG02451.hp1 HG02572.hp1 others(14): Show |
a0001 | a0001c0001a0001c0002a0001c0014 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(3): Show | a0001c0001t0001g0061a0001c0001t0001g0151a0001c0001t0001g0219others(14): Show | 17 | 246 | 0.0691 | -4 | c.-81 others(23): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144646401 | CTGTT | C | intron_variant | MODIFIER | HG00639.hp2 HG02683.hp1 HG02683.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0184a0001c0002t0001g0087a0001c0002t0001g0088others(1): Show | 4 | 246 | 0.0163 | -4 | c.-82 others(23): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144664718 | TCTTC | T | intron_variant | MODIFIER | HG02109.hp1 HG02622.hp2 HG02647.hp2 others(2): Show |
a0001 | a0001c0001a0001c0018 | a0001c0001t0001a0001c0018t0001 | a0001c0001t0001g0229a0001c0001t0001g0231a0001c0001t0001g0232others(2): Show | 5 | 246 | 0.0203 | -4 | c.-82 others(23): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38603407 | GTCTA | G | intron_variant | MODIFIER | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(59): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0002a0001c0004others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | a0001c0001t0001g0279a0001c0001t0002g0009a0001c0001t0002g0049others(53): Show | 62 | 350 | 0.1771 | -4 | c.137 others(21): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38603584 | ATCTC | A | intron_variant | MODIFIER | HG00438.hp2 HG00738.hp2 HG00741.hp2 others(94): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0002a0001c0004others(16): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(25): Show | a0001c0001t0001g0099a0001c0001t0002g0003a0001c0001t0002g0006others(84): Show | 97 | 350 | 0.2771 | -4 | c.137 others(21): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38603596 | GTCTC | G | intron_variant | MODIFIER | HG02572.hp1 HG02723.hp2 HG02976.hp2 others(7): Show |
a0001a0007a0019 | a0001c0008a0001c0021a0001c0038others(2): Show | a0001c0008t0004a0001c0008t0006a0001c0008t0007others(4): Show | a0001c0008t0004g0026a0001c0008t0004g0309a0001c0008t0006g0286others(6): Show | 10 | 350 | 0.0286 | -4 | c.137 others(21): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38627531 | ATGTG | A | intron_variant | MODIFIER | HG01361.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
a0003a0009 | a0003c0005a0003c0036a0009c0019others(1): Show | a0003c0005t0001a0003c0005t0002a0003c0036t0002others(3): Show | a0003c0005t0001g0138a0003c0005t0001g0196a0003c0005t0002g0008others(6): Show | 10 | 350 | 0.0286 | -4 | c.558 others(19): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38629982 | CAGAG | C | intron_variant | MODIFIER | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
a0005 | a0005c0006 | a0005c0006t0002 | a0005c0006t0002g0029a0005c0006t0002g0087a0005c0006t0002g0106others(1): Show | 5 | 350 | 0.0143 | -4 | c.783 others(19): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38630060 | TTTTC | T | intron_variant | MODIFIER | HG01261.hp1 HG01884.hp1 HG01891.hp2 others(3): Show |
a0008a0019 | a0008c0013a0008c0017a0019c0039 | a0008c0013t0008a0008c0017t0008a0019c0039t0013 | a0008c0013t0008g0028a0008c0013t0008g0303a0008c0017t0008g0046others(2): Show | 6 | 350 | 0.0171 | -4 | c.783 others(19): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38630080 | CTTTT | C | intron_variant | MODIFIER | HG01433.hp1 HG01496.hp2 HG01928.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0009 | a0001c0001t0003g0002a0001c0001t0003g0020a0001c0001t0003g0123others(1): Show | 8 | 350 | 0.0229 | -4 | c.783 others(19): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38630161 | CCCTT | C | intron_variant | MODIFIER | HG02258.hp1 HG02486.hp1 HG02572.hp1 others(4): Show |
a0001a0007 | a0001c0002a0001c0004a0001c0008others(1): Show | a0001c0002t0004a0001c0004t0016a0001c0008t0004others(2): Show | a0001c0002t0004g0073a0001c0004t0016g0231a0001c0008t0004g0026others(3): Show | 7 | 350 | 0.0200 | -4 | c.783 others(19): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38641079 | AGGAG | A | intron_variant | MODIFIER | HG00642.hp2 HG01516.hp2 HG01517.hp1 others(15): Show |
a0001a0002a0012others(1): Show | a0001c0001a0001c0004a0002c0003others(2): Show | a0001c0001t0005a0001c0004t0016a0002c0003t0004others(3): Show | a0001c0001t0005g0187a0001c0004t0016g0231a0002c0003t0004g0010others(13): Show | 18 | 350 | 0.0514 | -4 | c.128 others(21): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38643145 | CAAAA | C | intron_variant | MODIFIER | HG01109.hp1 HG02257.hp1 HG02896.hp2 others(4): Show |
a0007a0011 | a0007c0010a0007c0040a0011c0016 | a0007c0010t0010a0007c0010t0012a0007c0040t0004others(1): Show | a0007c0010t0010g0224a0007c0010t0010g0307a0007c0010t0012g0129others(4): Show | 7 | 350 | 0.0200 | -4 | c.136 others(21): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38647375 | TGTTG | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(218): Show |
a0001a0002a0004others(16): Show | a0001c0001a0001c0002a0001c0004others(26): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(38): Show | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(197): Show | 221 | 350 | 0.6314 | -4 | c.188 others(21): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38654114 | GATGA | G | downstream_gene_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(236): Show |
a0001a0002a0003others(16): Show | a0001c0001a0001c0002a0001c0004others(28): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(46): Show | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(214): Show | 239 | 350 | 0.6829 | -4 | c.*42 others(15): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3462 | chr20 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100692013 | GAAAT | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(50): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0002c0004others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(15): Show | a0001c0001t0001g0047a0001c0001t0001g0062a0001c0001t0001g0066others(50): Show | 53 | 286 | 0.1853 | -4 | c.154 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100692258 | ATTAT | A | intron_variant | MODIFIER | HG02895.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0009 | a0001c0001t0001a0002c0002t0008a0002c0002t0035others(1): Show | a0001c0001t0001g0093a0001c0001t0001g0095a0002c0002t0008g0009others(2): Show | 5 | 286 | 0.0175 | -4 | c.154 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100709573 | TGTGA | T | intron_variant | MODIFIER | HG00738.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0009 | a0001c0001t0001a0002c0002t0008a0002c0002t0035others(2): Show | a0001c0001t0001g0093a0001c0001t0001g0095a0002c0002t0008g0009others(3): Show | 6 | 286 | 0.0210 | -4 | c.154 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100714389 | TTGTG | T | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(58): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0002c0004others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(21): Show | a0001c0001t0001g0007a0001c0001t0001g0062a0001c0001t0001g0066others(58): Show | 61 | 286 | 0.2133 | -4 | c.154 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100728713 | CGTAT | C | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(39): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0010others(7): Show | a0001c0001t0001a0001c0001t0013a0001c0001t0034others(17): Show | a0001c0001t0001g0011a0001c0001t0001g0070a0001c0001t0001g0091others(39): Show | 42 | 286 | 0.1469 | -4 | c.154 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100728714 | GTATA | G | intron_variant | MODIFIER | HG00597.hp1 HG00733.hp1 HG00735.hp1 others(18): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0013a0001c0001t0024others(5): Show | a0001c0001t0001g0092a0001c0001t0001g0098a0001c0001t0001g0120others(18): Show | 21 | 286 | 0.0734 | -4 | c.154 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100729072 | GTCTC | G | intron_variant | MODIFIER | HG00673.hp2 HG02074.hp1 HG02080.hp2 others(10): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0013a0001c0003t0003others(1): Show | a0001c0001t0001g0271a0001c0001t0001g0275a0001c0001t0001g0276others(10): Show | 13 | 286 | 0.0455 | -4 | c.154 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100732886 | CTAAT | C | intron_variant | MODIFIER | HG01081.hp1 HG02055.hp2 HG02630.hp1 others(1): Show |
a0002 | a0002c0002a0002c0005 | a0002c0002t0002a0002c0002t0008a0002c0005t0010 | a0002c0002t0002g0139a0002c0002t0008g0028a0002c0002t0008g0029others(1): Show | 4 | 286 | 0.0140 | -4 | c.155 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100741344 | TCTTA | T | intron_variant | MODIFIER | HG00735.hp2 HG01346.hp1 HG01433.hp2 others(5): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0003t0014a0002c0002t0002others(3): Show | a0001c0001t0001g0011a0001c0003t0014g0234a0001c0003t0014g0235others(5): Show | 8 | 286 | 0.0280 | -4 | c.155 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100746169 | CTGAT | C | intron_variant | MODIFIER | HG00735.hp2 HG01346.hp1 HG01433.hp2 others(6): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0003t0014a0002c0002t0002others(4): Show | a0001c0001t0001g0011a0001c0003t0014g0234a0001c0003t0014g0235others(6): Show | 9 | 286 | 0.0315 | -4 | c.155 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100769712 | CTTTT | C | intron_variant | MODIFIER | HG00423.hp1 HG00673.hp1 HG01106.hp1 others(59): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0008others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0019others(17): Show | a0001c0001t0001g0092a0001c0001t0001g0129a0001c0001t0001g0177others(59): Show | 62 | 286 | 0.2168 | -4 | c.155 others(19): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100776981 | CAAAA | C | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0002c0002others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(20): Show | a0001c0001t0001g0007a0001c0001t0001g0062a0001c0001t0001g0066others(57): Show | 60 | 286 | 0.2098 | -4 | c.250 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100793669 | CACTT | C | intron_variant | MODIFIER | HG00408.hp2 HG00544.hp2 HG00733.hp2 others(46): Show |
a0001a0002 | a0001c0001a0001c0008a0001c0010others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0031others(15): Show | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0026others(46): Show | 49 | 286 | 0.1713 | -4 | c.251 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |