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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP6_chrX_11132544_11670920 | 11628984 | C | CGTGT | intron_variant | MODIFIER | HG00280.hp1 HG01243.hp1 HG03486.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002 | a0001c0001t0001a0001c0004t0005a0002c0002t0003others(1): Show | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0014 others(4): Show |
7 | 144 | 0.0486 | 4 | c.588 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11660530 | C | CAAAA | intron_variant | MODIFIER | HG00738.hp1 HG01069.hp1 HG02074.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(5): Show |
8 | 144 | 0.0556 | 4 | c.588 others(21): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44754338 | T | TTGTG | intron_variant | MODIFIER | HG01891.hp2 HG02129.hp1 HG02523.hp1 others(2): Show |
a0001a0002 | a0001c0004a0002c0003a0002c0006others(1): Show | a0001c0004t0001a0002c0003t0001a0002c0003t0004others(2): Show | a0001c0004t0001g0181 a0002c0003t0001g0387 a0002c0003t0004g0180 others(2): Show |
5 | 390 | 0.0128 | 4 | c.-72 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44754373 | T | TGTGA | intron_variant | MODIFIER | HG02273.hp2 HG03225.hp1 NA18988.hp2 |
a0001a0002a0003 | a0001c0004a0002c0019a0003c0005 | a0001c0004t0003a0002c0019t0008a0003c0005t0002 | a0001c0004t0003g0363 a0002c0019t0008g0313 a0003c0005t0002g0083 |
3 | 390 | 0.0077 | 4 | c.-72 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44767984 | C | CTTTT | intron_variant | MODIFIER | HG00099.hp2 HG01109.hp2 HG01256.hp2 others(17): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0007a0001c0017others(10): Show | a0001c0001t0003a0001c0007t0001a0001c0017t0001others(10): Show | a0001c0001t0003g0063 a0001c0001t0003g0153 a0001c0001t0003g0344 others(17): Show |
20 | 390 | 0.0513 | 4 | c.-72 others(23): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44771242 | A | ATTTT | intron_variant | MODIFIER | HG00597.hp2 HG02055.hp2 HG02135.hp1 others(3): Show |
a0001a0002a0003 | a0001c0001a0001c0021a0002c0013others(2): Show | a0001c0001t0003a0001c0001t0009a0001c0021t0001others(3): Show | a0001c0001t0003g0006 a0001c0001t0009g0173 a0001c0021t0001g0033 others(3): Show |
6 | 390 | 0.0154 | 4 | c.-71 others(23): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44777998 | T | TTTTA | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(26): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0004a0001c0008others(11): Show | a0001c0001t0003a0001c0004t0001a0001c0004t0003others(14): Show | a0001c0001t0003g0159 a0001c0001t0003g0305 a0001c0004t0001g0136 others(26): Show |
29 | 390 | 0.0744 | 4 | c.-71 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44779564 | A | ATTTT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
a0001a0002a0003others(20): Show | a0001c0001a0001c0004a0001c0007others(50): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(59): Show | a0001c0001t0001g0024 a0001c0001t0001g0042 a0001c0001t0001g0097 others(213): Show |
216 | 390 | 0.5539 | 4 | c.-71 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44783054 | C | CCCCT | intron_variant | MODIFIER | HG02896.hp1 HG02897.hp2 HG03130.hp2 others(1): Show |
a0001a0002a0003 | a0001c0007a0002c0023a0003c0005 | a0001c0007t0001a0002c0023t0005a0003c0005t0012 | a0001c0007t0001g0069 a0002c0023t0005g0071 a0002c0023t0005g0072 others(1): Show |
4 | 390 | 0.0103 | 4 | c.-71 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44792021 | C | CTTTT | intron_variant | MODIFIER | HG00280.hp1 HG00621.hp1 HG01256.hp1 others(32): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0004a0001c0007others(16): Show | a0001c0001t0001a0001c0001t0010a0001c0004t0003others(18): Show | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0010g0198 others(32): Show |
35 | 390 | 0.0897 | 4 | c.79+ others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44795040 | C | CAAAA | intron_variant | MODIFIER | HG01934.hp1 HG02109.hp2 HG02615.hp2 others(12): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0007a0002c0011others(6): Show | a0001c0001t0009a0001c0007t0001a0002c0011t0005others(6): Show | a0001c0001t0009g0173 a0001c0001t0009g0321 a0001c0007t0001g0058 others(12): Show |
15 | 390 | 0.0385 | 4 | c.80- others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44813790 | C | CACTT | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(137): Show |
a0001a0002a0003others(15): Show | a0001c0001a0001c0004a0001c0007others(33): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(39): Show | a0001c0001t0001g0024 a0001c0001t0001g0134 a0001c0001t0001g0161 others(137): Show |
140 | 390 | 0.3590 | 4 | c.300 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44816803 | C | CAAAA | intron_variant | MODIFIER | HG01517.hp2 HG02027.hp2 HG02055.hp2 others(4): Show |
a0001a0002a0003 | a0001c0001a0001c0009a0001c0017others(3): Show | a0001c0001t0003a0001c0009t0001a0001c0017t0001others(3): Show | a0001c0001t0003g0260 a0001c0009t0001g0317 a0001c0017t0001g0125 others(4): Show |
7 | 390 | 0.0180 | 4 | c.386 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44818705 | C | CTCTT | intron_variant | MODIFIER | HG01496.hp2 HG02258.hp2 HG02280.hp1 others(22): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0007a0001c0008others(11): Show | a0001c0001t0003a0001c0007t0001a0001c0008t0001others(11): Show | a0001c0001t0003g0063 a0001c0007t0001g0058 a0001c0007t0001g0202 others(22): Show |
25 | 390 | 0.0641 | 4 | c.387 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44821914 | T | TAGAG | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(144): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0004a0001c0007others(24): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(30): Show | a0001c0001t0001g0024 a0001c0001t0001g0097 a0001c0001t0001g0370 others(144): Show |
147 | 390 | 0.3769 | 4 | c.387 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44827336 | G | GGTTT | intron_variant | MODIFIER | HG02559.hp2 HG02809.hp1 HG03516.hp1 |
a0001a0002 | a0001c0007a0002c0011a0002c0019 | a0001c0007t0001a0002c0011t0005a0002c0019t0008 | a0001c0007t0001g0324 a0002c0011t0005g0016 a0002c0019t0008g0046 |
3 | 390 | 0.0077 | 4 | c.596 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | chr22 | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44827336 | G | GTTTT | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(95): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0004a0001c0007others(22): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0011others(25): Show | a0001c0001t0001g0097 a0001c0001t0001g0192 a0001c0001t0001g0200 others(95): Show |
98 | 390 | 0.2513 | 4 | c.596 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44829118 | C | CAAAA | intron_variant | MODIFIER | HG02451.hp2 HG02630.hp2 HG03492.hp1 others(3): Show |
a0001a0002a0003 | a0001c0007a0001c0008a0002c0006others(2): Show | a0001c0007t0001a0001c0008t0001a0002c0006t0001others(2): Show | a0001c0007t0001g0304 a0001c0007t0001g0382 a0001c0008t0001g0038 others(3): Show |
6 | 390 | 0.0154 | 4 | c.596 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44833097 | T | TTTTC | intron_variant | MODIFIER | HG01109.hp2 HG02258.hp1 HG02559.hp1 others(7): Show |
a0002a0007a0009others(1): Show | a0002c0067a0007c0027a0007c0030others(3): Show | a0002c0067t0005a0007c0027t0001a0007c0030t0001others(3): Show | a0002c0067t0005g0067 a0007c0027t0001g0314 a0007c0027t0001g0346 others(7): Show |
10 | 390 | 0.0256 | 4 | c.596 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44833344 | G | GTGGT | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(61): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0004a0001c0007others(11): Show | a0001c0001t0003a0001c0004t0001a0001c0004t0003others(14): Show | a0001c0001t0003g0089 a0001c0001t0003g0157 a0001c0001t0003g0159 others(61): Show |
64 | 390 | 0.1641 | 4 | c.596 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44835231 | C | CTATA | intron_variant | MODIFIER | HG01109.hp2 HG02809.hp2 HG02976.hp1 others(2): Show |
a0001a0002a0007 | a0001c0001a0002c0067a0007c0027 | a0001c0001t0003a0001c0001t0009a0002c0067t0005others(1): Show | a0001c0001t0003g0063 a0001c0001t0009g0173 a0001c0001t0009g0321 others(2): Show |
5 | 390 | 0.0128 | 4 | c.596 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44842357 | A | AAAAC | intron_variant | MODIFIER | HG01934.hp1 HG02109.hp2 NA18906.hp2 |
a0002a0012 | a0002c0020a0012c0035 | a0002c0020t0005a0012c0035t0001 | a0002c0020t0005g0355 a0012c0035t0001g0001 a0012c0035t0001g0045 |
3 | 390 | 0.0077 | 4 | c.597 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44851393 | A | ATATT | intron_variant | MODIFIER | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(15): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0004a0002c0015others(6): Show | a0001c0001t0001a0001c0004t0001a0001c0004t0003others(8): Show | a0001c0001t0001g0097 a0001c0001t0001g0370 a0001c0004t0001g0136 others(15): Show |
18 | 390 | 0.0462 | 4 | c.877 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44856254 | C | CTTTT | intron_variant | MODIFIER | HG01934.hp1 HG02572.hp1 HG02818.hp2 others(6): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0007a0001c0017others(4): Show | a0001c0001t0001a0001c0007t0001a0001c0017t0001others(4): Show | a0001c0001t0001g0370 a0001c0007t0001g0324 a0001c0007t0001g0356 others(6): Show |
9 | 390 | 0.0231 | 4 | c.878 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44857929 | A | ATTTC | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0004a0001c0008others(31): Show | a0001c0001t0003a0001c0001t0009a0001c0001t0010others(39): Show | a0001c0001t0003g0006 a0001c0001t0003g0023 a0001c0001t0003g0028 others(124): Show |
127 | 390 | 0.3256 | 4 | c.878 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44857945 | C | CAGTG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
a0001a0002a0003others(26): Show | a0001c0001a0001c0004a0001c0007others(69): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(86): Show | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0097 others(301): Show |
304 | 390 | 0.7795 | 4 | c.878 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44858533 | C | CTTTT | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(131): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0004a0001c0038others(27): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0003others(31): Show | a0001c0001t0001g0042 a0001c0001t0003g0156 a0001c0004t0003g0118 others(131): Show |
134 | 390 | 0.3436 | 4 | c.878 others(21): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44861545 | G | GCCTC | intron_variant | MODIFIER | HG03490.hp1 HG03492.hp2 NA18939.hp1 others(3): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0003a0001c0004t0003 | a0001c0001t0003g0080 a0001c0001t0003g0109 a0001c0001t0003g0110 others(3): Show |
6 | 390 | 0.0154 | 4 | c.982 others(19): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGDIB_chr12_14937031_14966601 | 14940736 | T | TAAAC | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(7): Show | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0039 others(73): Show |
94 | 464 | 0.2026 | 4 | c.*17 others(15): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1294 | chr12 | TogoVar | |||||||
ARHGDIB_chr12_14937031_14966601 | 14948099 | T | TGCGC | intron_variant | MODIFIER | HG00639.hp2 HG02155.hp1 HG03942.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0053 a0001c0001t0001g0145 a0001c0001t0001g0147 others(1): Show |
5 | 464 | 0.0108 | 4 | c.266 others(19): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | TogoVar | |||||||
ARHGDIB_chr12_14937031_14966601 | 14948100 | G | GCACA | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp2 HG00741.hp1 others(54): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0005a0001c0002t0001others(2): Show | a0001c0001t0001g0006 a0001c0001t0001g0033 a0001c0001t0001g0059 others(31): Show |
57 | 464 | 0.1228 | 4 | c.266 others(19): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | TogoVar | |||||||
ARHGEF10L_chr1_17534698_17702869 | 17544291 | T | TATGA | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(10): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0005a0001c0040others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0005t0001others(6): Show | a0001c0001t0001g0118 a0001c0001t0001g0124 a0001c0001t0001g0127 others(10): Show |
13 | 168 | 0.0774 | 4 | c.-44 others(21): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17548646 | C | CTTTT | intron_variant | MODIFIER | HG02559.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0017a0001c0034others(4): Show | a0001c0001t0003a0001c0017t0002a0001c0034t0002others(4): Show | a0001c0001t0003g0114 a0001c0017t0002g0113 a0001c0034t0002g0110 others(4): Show |
7 | 168 | 0.0417 | 4 | c.-44 others(21): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17588849 | A | AGTGT | intron_variant | MODIFIER | HG00323.hp2 HG00738.hp1 HG00738.hp2 others(7): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0012a0001c0013others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0012t0001others(6): Show | a0001c0001t0001g0002 a0001c0001t0001g0096 a0001c0001t0003g0168 others(7): Show |
10 | 168 | 0.0595 | 4 | c.257 others(19): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17611533 | T | TATCC | intron_variant | MODIFIER | HG00323.hp1 HG01106.hp2 HG01169.hp1 others(21): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0012a0001c0019others(11): Show | a0001c0001t0001a0001c0012t0001a0001c0019t0001others(11): Show | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0045 others(21): Show |
24 | 168 | 0.1429 | 4 | c.610 others(21): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17611977 | G | GTCCA | intron_variant | MODIFIER | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(39): Show |
a0001a0002a0004others(9): Show | a0001c0001a0001c0005a0001c0011others(21): Show | a0001c0001t0001a0001c0001t0003a0001c0005t0003others(22): Show | a0001c0001t0001g0095 a0001c0001t0001g0140 a0001c0001t0003g0114 others(39): Show |
42 | 168 | 0.2500 | 4 | c.610 others(21): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17655437 | G | GTCCA | intron_variant | MODIFIER | HG00558.hp1 HG06807.hp2 NA18747.hp1 others(1): Show |
a0001 | a0001c0001a0001c0019 | a0001c0001t0001a0001c0019t0001 | a0001c0001t0001g0011 a0001c0001t0001g0071 a0001c0001t0001g0159 others(1): Show |
4 | 168 | 0.0238 | 4 | c.248 others(21): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17686078 | T | TTTTC | intron_variant | MODIFIER | HG00558.hp2 HG01257.hp2 HG01258.hp1 others(12): Show |
a0001a0003a0008others(1): Show | a0001c0001a0003c0002a0008c0041others(1): Show | a0001c0001t0001a0001c0001t0003a0003c0002t0001others(2): Show | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0012 others(12): Show |
15 | 168 | 0.0893 | 4 | c.301 others(23): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1821139 | C | CAAAA | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(19): Show |
a0001a0002a0003others(2): Show | a0001c0003a0001c0004a0001c0009others(15): Show | a0001c0003t0008a0001c0004t0005a0001c0009t0005others(18): Show | a0001c0003t0008g0288 a0001c0004t0005g0299 a0001c0009t0005g0287 others(19): Show |
22 | 363 | 0.0606 | 4 | c.-30 others(15): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2786 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1824899 | C | CACCT | intron_variant | MODIFIER | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
a0001a0002a0004others(6): Show | a0001c0001a0001c0003a0001c0004others(25): Show | a0001c0001t0006a0001c0003t0007a0001c0003t0021others(32): Show | a0001c0001t0006g0098 a0001c0001t0006g0115 a0001c0003t0007g0102 others(33): Show |
37 | 363 | 0.1019 | 4 | c.-48 others(19): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1832753 | C | CAGAG | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0002a0001c0003others(65): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0014others(95): Show | a0001c0001t0002g0030 a0001c0001t0002g0053 a0001c0001t0002g0066 others(135): Show |
138 | 363 | 0.3802 | 4 | c.-48 others(21): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1832835 | C | CAGAG | intron_variant | MODIFIER | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(67): Show |
a0001a0002a0006others(5): Show | a0001c0001a0001c0002a0001c0003others(40): Show | a0001c0001t0004a0001c0001t0014a0001c0001t0019others(51): Show | a0001c0001t0004g0022 a0001c0001t0004g0138 a0001c0001t0004g0141 others(67): Show |
70 | 363 | 0.1928 | 4 | c.-48 others(21): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1833021 | C | CAGAG | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0002a0001c0003others(66): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0014others(96): Show | a0001c0001t0002g0030 a0001c0001t0002g0053 a0001c0001t0002g0066 others(134): Show |
137 | 363 | 0.3774 | 4 | c.-48 others(21): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1833119 | G | GAGAC | intron_variant | MODIFIER | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(29): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0003a0001c0004others(23): Show | a0001c0001t0006a0001c0003t0003a0001c0003t0035others(25): Show | a0001c0001t0006g0098 a0001c0001t0006g0115 a0001c0003t0003g0161 others(28): Show |
32 | 363 | 0.0882 | 4 | c.-48 others(21): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1839677 | A | ACTGT | intron_variant | MODIFIER | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(143): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0002a0001c0003others(79): Show | a0001c0001t0002a0001c0001t0019a0001c0002t0001others(102): Show | a0001c0001t0002g0224 a0001c0001t0002g0239 a0001c0001t0019g0278 others(143): Show |
146 | 363 | 0.4022 | 4 | c.-47 others(21): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1857875 | G | GATCT | intron_variant | MODIFIER | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(54): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0002a0001c0003others(37): Show | a0001c0001t0002a0001c0001t0014a0001c0002t0001others(44): Show | a0001c0001t0002g0239 a0001c0001t0002g0271 a0001c0001t0014g0361 others(54): Show |
57 | 363 | 0.1570 | 4 | c.38- others(15): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1857879 | G | GATCT | intron_variant | MODIFIER | HG00423.hp1 HG00544.hp1 HG01070.hp1 others(25): Show |
a0001a0002a0006others(3): Show | a0001c0001a0001c0002a0001c0040others(22): Show | a0001c0001t0002a0001c0002t0020a0001c0002t0049others(23): Show | a0001c0001t0002g0030 a0001c0002t0020g0206 a0001c0002t0049g0021 others(24): Show |
28 | 363 | 0.0771 | 4 | c.38- others(15): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1871112 | C | CAAAA | intron_variant | MODIFIER | HG00408.hp1 HG02280.hp2 HG02615.hp2 others(12): Show |
a0001a0003a0004others(2): Show | a0001c0001a0001c0002a0001c0009others(7): Show | a0001c0001t0002a0001c0001t0004a0001c0002t0001others(9): Show | a0001c0001t0002g0271 a0001c0001t0004g0354 a0001c0002t0001g0211 others(12): Show |
15 | 363 | 0.0413 | 4 | c.679 others(21): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1873510 | T | TTGCG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
a0001a0002a0003others(16): Show | a0001c0001a0001c0002a0001c0003others(103): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0019others(144): Show | a0001c0001t0002g0069 a0001c0001t0002g0239 a0001c0001t0004g0354 others(187): Show |
191 | 363 | 0.5262 | 4 | c.680 others(21): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1873510 | T | TTTCA | intron_variant | MODIFIER | HG00408.hp1 HG00621.hp2 HG02280.hp2 others(17): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0002a0001c0005others(9): Show | a0001c0001t0002a0001c0001t0012a0001c0002t0001others(11): Show | a0001c0001t0002g0224 a0001c0001t0002g0271 a0001c0001t0012g0207 others(17): Show |
20 | 363 | 0.0551 | 4 | c.680 others(21): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar |