view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | 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 | 46888333 | TAC | T | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(100): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0007a0001c0009others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(33): Show | a0001c0001t0001g0068 a0001c0001t0001g0119 a0001c0001t0003g0001 others(100): Show |
103 | 298 | 0.3456 | -2 | c.-18 others(23): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46909054 | CTT | C | intron_variant | MODIFIER | HG00642.hp1 HG01070.hp1 HG01071.hp2 others(19): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0019a0001c0001t0027a0001c0001t0029others(7): Show | a0001c0001t0019g0024 a0001c0001t0019g0219 a0001c0001t0027g0034 others(19): Show |
22 | 298 | 0.0738 | -2 | c.-18 others(21): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46939027 | GAA | G | intron_variant | MODIFIER | HG01069.hp2 HG01261.hp2 HG02074.hp1 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0009 | a0001c0001t0001g0134 a0001c0001t0002g0131 a0001c0001t0002g0132 others(13): Show |
16 | 298 | 0.0537 | -2 | c.382 others(21): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46976210 | CTT | C | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(27): Show |
a0001a0003 | a0001c0001a0003c0013 | a0001c0001t0004a0001c0001t0022a0001c0001t0032others(3): Show | a0001c0001t0004g0022 a0001c0001t0004g0070 a0001c0001t0004g0071 others(27): Show |
30 | 298 | 0.1007 | -2 | 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 | 46983054 | CAA | C | intron_variant | MODIFIER | HG00639.hp2 HG01070.hp2 HG01071.hp2 others(41): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(15): Show | a0001c0001t0001g0119 a0001c0001t0005g0102 a0001c0001t0005g0106 others(41): Show |
44 | 298 | 0.1477 | -2 | c.382 others(21): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 47003916 | ACG | A | 3_prime_UTR_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(74): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0003a0001c0001t0010a0001c0001t0011others(20): Show | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0004 others(74): Show |
77 | 298 | 0.2584 | -2 | c.*32 others(13): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 47006267 | CTT | C | downstream_gene_variant | MODIFIER | HG00621.hp1 HG00735.hp2 HG01099.hp1 others(47): Show |
a0001a0003 | a0001c0001a0003c0013 | a0001c0001t0004a0001c0001t0005a0001c0001t0008others(11): Show | a0001c0001t0004g0070 a0001c0001t0004g0071 a0001c0001t0004g0076 others(47): Show |
50 | 298 | 0.1678 | -2 | c.*55 others(13): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1191 | chr19 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 47007073 | CTT | C | downstream_gene_variant | MODIFIER | HG02080.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0014a0001c0001t0056 | a0001c0001t0003g0031 a0001c0001t0014g0069 a0001c0001t0014g0087 others(3): Show |
6 | 298 | 0.0201 | -2 | c.*63 others(13): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1997 | chr19 | TogoVar | |||||||
ARHGAP36_chrX_131053346_131094885 | 131065041 | TTG | T | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(251): Show |
a0000a0001a0002 | a0000c0003a0001c0001a0001c0004others(1): Show | a0000c0003t0007a0001c0001t0001a0001c0001t0002others(8): Show | a0000c0003t0007g0096 a0001c0001t0001g0001 a0001c0001t0001g0004 others(183): Show |
254 | 302 | 0.8411 | -2 | c.-14 others(21): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131074338 | AGT | A | intron_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0171 a0001c0001t0001g0221 a0001c0001t0001g0222 others(11): Show |
15 | 302 | 0.0497 | -2 | c.-14 others(21): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131074358 | TGA | T | intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0168 | 1 | 302 | 0.0033 | -2 | c.-14 others(21): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131074439 | ATG | A | intron_variant | MODIFIER | HG01261.hp1 HG01346.hp1 HG01975.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0171 a0001c0001t0002g0023 a0001c0001t0003g0161 others(6): Show |
10 | 302 | 0.0331 | -2 | c.-14 others(21): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131075537 | AAC | A | intron_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0004g0029 others(2): Show |
5 | 302 | 0.0166 | -2 | c.-14 others(21): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131075615 | GTA | G | intron_variant | MODIFIER | HG02896.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006 | a0001c0001t0001g0171 a0001c0001t0002g0023 a0001c0001t0006g0166 others(1): Show |
5 | 302 | 0.0166 | -2 | c.-14 others(21): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131075623 | ATG | A | intron_variant | MODIFIER | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(110): Show |
a0000a0001 | a0000c0003a0001c0001 | a0000c0003t0007a0001c0001t0001a0001c0001t0002others(4): Show | a0000c0003t0007g0096 a0001c0001t0001g0013 a0001c0001t0001g0014 others(85): Show |
113 | 302 | 0.3742 | -2 | c.-14 others(21): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131077764 | CAT | C | intron_variant | MODIFIER | HG00609.hp1 HG02027.hp1 HG02071.hp1 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0127 a0001c0001t0001g0136 a0001c0001t0002g0003 others(4): Show |
15 | 302 | 0.0497 | -2 | c.-14 others(21): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131078231 | CTG | C | intron_variant | MODIFIER | HG00741.hp1 HG01993.hp1 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0112 a0001c0001t0004g0113 |
2 | 302 | 0.0066 | -2 | c.-14 others(21): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131079560 | TTG | T | intron_variant | MODIFIER | NA18522.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0171 | 1 | 302 | 0.0033 | -2 | c.-14 others(21): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131080398 | TAA | T | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(104): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(70): Show |
107 | 302 | 0.3543 | -2 | c.-14 others(21): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144528689 | GCC | G | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(49): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0010others(3): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0011others(7): Show | a0001c0001t0001g0016 a0001c0001t0001g0030 a0001c0001t0001g0033 others(49): Show |
52 | 246 | 0.2114 | -2 | c.*17 others(13): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 489 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144534901 | CAG | C | intron_variant | MODIFIER | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(8): Show |
a0001 | a0001c0001a0001c0007a0001c0018 | a0001c0001t0001a0001c0007t0001a0001c0018t0001 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(8): Show |
11 | 246 | 0.0447 | -2 | c.261 others(19): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 7/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144538974 | CCT | C | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(72): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(7): Show | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0029 others(72): Show |
75 | 246 | 0.3049 | -2 | c.252 others(21): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144559354 | CAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(12): Show | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0027 others(71): Show |
74 | 246 | 0.3008 | -2 | c.513 others(19): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144566086 | CCT | C | intron_variant | MODIFIER | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(16): Show |
a0001 | a0001c0001a0001c0002a0001c0014others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(4): Show | a0001c0001t0001g0024 a0001c0001t0001g0151 a0001c0001t0004g0150 others(16): Show |
19 | 246 | 0.0772 | -2 | c.513 others(21): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144566862 | GAA | G | intron_variant | MODIFIER | HG02055.hp2 HG02145.hp1 HG02572.hp1 others(14): Show |
a0001 | a0001c0001a0001c0002a0001c0014others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(4): Show | a0001c0001t0001g0024 a0001c0001t0001g0151 a0001c0001t0004g0150 others(14): Show |
17 | 246 | 0.0691 | -2 | c.513 others(21): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144567976 | ATC | A | intron_variant | MODIFIER | HG01981.hp2 HG02080.hp1 NA18962.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0132 a0001c0001t0001g0144 a0001c0002t0001g0035 |
3 | 246 | 0.0122 | -2 | c.513 others(21): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144576332 | CAA | C | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(19): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0003a0001c0005others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(11): Show | a0001c0001t0001g0016 a0001c0001t0003g0063 a0001c0001t0003g0068 others(19): Show |
22 | 246 | 0.0894 | -2 | c.512 others(19): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144594694 | CAA | C | intron_variant | MODIFIER | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
a0001 | a0001c0004 | a0001c0004t0006 | a0001c0004t0006g0069 a0001c0004t0006g0070 a0001c0004t0006g0073 others(2): Show |
5 | 246 | 0.0203 | -2 | c.80+ others(19): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144594757 | CAT | C | intron_variant | MODIFIER | HG02280.hp1 HG02451.hp2 HG02622.hp1 others(5): Show |
a0001a0005 | a0001c0001a0001c0004a0001c0007others(1): Show | a0001c0001t0007a0001c0004t0006a0001c0007t0001others(1): Show | a0001c0001t0007g0018 a0001c0004t0006g0069 a0001c0004t0006g0070 others(5): Show |
8 | 246 | 0.0325 | -2 | c.80+ others(19): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144600924 | CTG | C | intron_variant | MODIFIER | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0017 | a0001c0001t0001a0001c0001t0004a0001c0002t0001others(1): Show | a0001c0001t0001g0024 a0001c0001t0001g0151 a0001c0001t0004g0150 others(8): Show |
11 | 246 | 0.0447 | -2 | c.80+ others(17): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144601154 | CTG | C | intron_variant | MODIFIER | HG01175.hp1 HG02027.hp1 HG02257.hp1 others(3): Show |
a0001 | a0001c0002a0001c0003a0001c0007 | a0001c0002t0001a0001c0003t0001a0001c0007t0003 | a0001c0002t0001g0007 a0001c0002t0001g0095 a0001c0002t0001g0096 others(3): Show |
6 | 246 | 0.0244 | -2 | c.80+ others(17): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144601308 | CTG | C | intron_variant | MODIFIER | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0007others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0001others(2): Show | a0001c0001t0001g0024 a0001c0001t0001g0151 a0001c0001t0004g0150 others(9): Show |
12 | 246 | 0.0488 | -2 | c.80+ others(17): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144601488 | CTG | C | intron_variant | MODIFIER | HG02109.hp1 HG02559.hp2 HG02615.hp2 others(10): Show |
a0001 | a0001c0001a0001c0018 | a0001c0001t0001a0001c0001t0002a0001c0018t0001 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(10): Show |
13 | 246 | 0.0529 | -2 | c.80+ others(17): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144601784 | CGT | C | intron_variant | MODIFIER | HG00558.hp2 HG00609.hp2 HG01975.hp2 others(15): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0012others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(2): Show | a0001c0001t0001g0061 a0001c0001t0001g0132 a0001c0001t0001g0135 others(15): Show |
18 | 246 | 0.0732 | -2 | c.80+ others(17): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144601801 | CTG | C | intron_variant | MODIFIER | HG01099.hp1 HG02630.hp1 HG02735.hp1 others(1): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0007others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0007t0003others(1): Show | a0001c0001t0001g0203 a0001c0002t0001g0119 a0001c0007t0003g0118 others(1): Show |
4 | 246 | 0.0163 | -2 | c.80+ others(17): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144601879 | CTG | C | intron_variant | MODIFIER | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0018a0001c0001t0021 | a0001c0001t0003g0023 a0001c0001t0018g0022 a0001c0001t0021g0062 |
3 | 246 | 0.0122 | -2 | c.80+ others(17): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144602633 | CGT | C | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(66): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0013others(10): Show | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0057 others(66): Show |
69 | 246 | 0.2805 | -2 | c.80+ others(17): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144602847 | CGT | C | intron_variant | MODIFIER | HG02027.hp2 HG02132.hp1 HG02135.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0204 others(2): Show |
5 | 246 | 0.0203 | -2 | c.80+ others(17): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144602903 | CTG | C | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(10): Show |
a0001a0003a0004 | a0001c0001a0001c0003a0001c0005others(3): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0009others(5): Show | a0001c0001t0001g0228 a0001c0003t0001g0005 a0001c0003t0001g0012 others(10): Show |
13 | 246 | 0.0529 | -2 | c.80+ others(17): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144603044 | CGT | C | intron_variant | MODIFIER | HG02258.hp1 HG03209.hp1 HG03453.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0018a0001c0001t0021 | a0001c0001t0003g0023 a0001c0001t0018g0022 a0001c0001t0021g0062 |
3 | 246 | 0.0122 | -2 | c.80+ others(17): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144619717 | CAT | C | intron_variant | MODIFIER | HG01981.hp2 NA18962.hp2 NA18967.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0132 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | 246 | 0.0122 | -2 | c.-81 others(21): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144638678 | CTT | C | intron_variant | MODIFIER | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0002t0001 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(5): Show |
8 | 246 | 0.0325 | -2 | c.-81 others(21): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144656194 | GAA | G | intron_variant | MODIFIER | HG02559.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0002t0001 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(5): Show |
8 | 246 | 0.0325 | -2 | c.-82 others(21): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144682548 | CAA | C | intron_variant | MODIFIER | HG02258.hp1 HG02280.hp1 HG02293.hp1 others(16): Show |
a0001 | a0001c0001a0001c0002a0001c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0055 others(16): Show |
19 | 246 | 0.0772 | -2 | c.-82 others(19): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144689426 | CTT | C | upstream_gene_variant | MODIFIER | HG01081.hp1 HG02145.hp1 HG02896.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0016 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0148 a0001c0001t0002g0235 a0001c0001t0003g0063 others(5): Show |
8 | 246 | 0.0325 | -2 | c.-38 others(13): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3581 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144690811 | ATT | A | upstream_gene_variant | MODIFIER | HG02451.hp2 HG02717.hp2 HG02886.hp1 others(4): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0007a0001c0004t0006 | a0001c0001t0001g0016 a0001c0001t0007g0018 a0001c0004t0006g0069 others(4): Show |
7 | 246 | 0.0285 | -2 | c.-52 others(13): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 4966 | chr8 | TogoVar | |||||||
ARHGAP40_chr20_38596809_38655653 | 38627531 | ATG | A | intron_variant | MODIFIER | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(71): Show |
a0001a0004a0006others(6): Show | a0001c0002a0001c0008a0004c0011others(8): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(17): Show | a0001c0002t0001g0025 a0001c0002t0001g0125 a0001c0002t0001g0126 others(67): Show |
74 | 350 | 0.2114 | -2 | c.558 others(17): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38627682 | GTT | G | intron_variant | MODIFIER | HG02886.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
a0005 | a0005c0006 | a0005c0006t0002 | a0005c0006t0002g0029 a0005c0006t0002g0087 a0005c0006t0002g0106 others(1): Show |
5 | 350 | 0.0143 | -2 | c.558 others(17): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | chr20 | TogoVar | |||||||
ARHGAP40_chr20_38596809_38655653 | 38639003 | CAG | C | intron_variant | MODIFIER | HG01891.hp1 HG02109.hp2 HG02572.hp2 |
a0003a0009 | a0003c0005a0009c0019 | a0003c0005t0001a0009c0019t0007 | a0003c0005t0001g0138 a0003c0005t0001g0196 a0009c0019t0007g0311 |
3 | 350 | 0.0086 | -2 | c.111 others(19): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38640123 | TCC | T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
a0001a0002a0009others(5): Show | a0001c0001a0001c0002a0001c0004others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0023 others(151): Show |
172 | 350 | 0.4914 | -2 | c.127 others(19): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 9/14 | chr20 | TogoVar |