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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGEF10L_chr1_17534698_17702869 | 17611533 | TATCC | T | intron_variant | MODIFIER | HG00733.hp1 HG01074.hp2 HG01106.hp1 others(24): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0017a0001c0043others(13): Show | a0001c0001t0001a0001c0017t0002a0001c0043t0002others(13): Show | a0001c0001t0001g0140a0001c0017t0002g0113a0001c0017t0002g0148others(24): Show | 27 | 168 | 0.1607 | -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 | GTCCA | G | intron_variant | MODIFIER | HG00558.hp2 HG01069.hp1 HG01069.hp2 others(76): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0006a0001c0013others(20): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(25): Show | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(76): Show | 79 | 168 | 0.4702 | -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 | TTTTC | T | intron_variant | MODIFIER | HG00741.hp1 HG01109.hp1 HG01257.hp1 others(2): Show |
a0001 | a0001c0011a0001c0020a0001c0042 | a0001c0011t0001a0001c0020t0001a0001c0042t0001 | a0001c0011t0001g0004a0001c0011t0001g0138a0001c0011t0001g0152others(2): Show | 5 | 168 | 0.0298 | -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 | 1825345 | CCTCT | C | intron_variant | MODIFIER | HG01123.hp1 HG02647.hp2 HG02723.hp2 |
a0001a0010 | a0001c0020a0010c0097a0010c0098 | a0001c0020t0015a0010c0097t0014a0010c0098t0003 | a0001c0020t0015g0204a0010c0097t0014g0205a0010c0098t0003g0203 | 3 | 363 | 0.0083 | -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 | 1826354 | GTGTT | G | intron_variant | MODIFIER | HG02257.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
a0001 | a0001c0046a0001c0047a0001c0123 | a0001c0046t0001a0001c0047t0009a0001c0123t0001 | a0001c0046t0001g0332a0001c0046t0001g0333a0001c0047t0009g0331others(2): Show | 5 | 363 | 0.0138 | -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 | 1833351 | CAGAG | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0002a0001c0003others(65): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0014others(96): Show | a0001c0001t0002g0030a0001c0001t0002g0053a0001c0001t0002g0066others(136): Show | 139 | 363 | 0.3829 | -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 | 1855085 | AATTC | A | intron_variant | MODIFIER | HG00597.hp2 HG01361.hp1 HG01884.hp2 others(16): Show |
a0001a0002a0004others(1): Show | a0001c0003a0001c0004a0001c0006others(14): Show | a0001c0003t0051a0001c0004t0048a0001c0006t0001others(15): Show | a0001c0003t0051g0118a0001c0004t0048g0104a0001c0006t0001g0008others(16): Show | 19 | 363 | 0.0523 | -4 | c.38- others(19): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1857870 | AGATC | A | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(87): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0001c0003others(58): Show | a0001c0001t0002a0001c0001t0006a0001c0002t0001others(74): Show | a0001c0001t0002g0224a0001c0001t0006g0115a0001c0002t0001g0211others(87): Show | 90 | 363 | 0.2479 | -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 | GATCT | G | intron_variant | MODIFIER | HG00642.hp1 HG01081.hp2 HG01106.hp1 others(11): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0002a0001c0001t0004a0001c0002t0003others(10): Show | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0001t0004g0168others(11): Show | 14 | 363 | 0.0386 | -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 | 1866422 | GACAC | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(115): Show |
a0001a0002a0004others(8): Show | a0001c0001a0001c0002a0001c0003others(57): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0012others(77): Show | a0001c0001t0002g0224a0001c0001t0002g0271a0001c0001t0004g0354others(115): Show | 118 | 363 | 0.3251 | -4 | c.546 others(17): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 5/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1887482 | CTGAG | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(94): Show |
a0001a0003a0006others(3): Show | a0001c0001a0001c0002a0001c0003others(45): Show | a0001c0001t0002a0001c0001t0012a0001c0002t0001others(62): Show | a0001c0001t0002g0053a0001c0001t0002g0066a0001c0001t0012g0207others(94): Show | 97 | 363 | 0.2672 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1887964 | CACTG | C | intron_variant | MODIFIER | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(16): Show |
a0002a0014a0018 | a0002c0025a0002c0028a0002c0032others(14): Show | a0002c0025t0024a0002c0025t0059a0002c0028t0001others(15): Show | a0002c0025t0024g0106a0002c0025t0059g0105a0002c0028t0001g0223others(16): Show | 19 | 363 | 0.0523 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1888112 | CACTT | C | intron_variant | MODIFIER | HG03669.hp1 HG03831.hp1 HG04228.hp2 |
a0001a0003 | a0001c0009a0001c0018a0003c0051 | a0001c0009t0069a0001c0018t0028a0003c0051t0006 | a0001c0009t0069g0302a0001c0018t0028g0146a0003c0051t0006g0319 | 3 | 363 | 0.0083 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1888200 | ACACT | A | intron_variant | MODIFIER | HG02145.hp1 NA18982.hp1 NA18994.hp1 others(1): Show |
a0001 | a0001c0005a0001c0006a0001c0021others(1): Show | a0001c0005t0001a0001c0006t0001a0001c0021t0002others(1): Show | a0001c0005t0001g0325a0001c0006t0001g0264a0001c0021t0002g0321others(1): Show | 4 | 363 | 0.0110 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1888230 | CAGTG | C | intron_variant | MODIFIER | HG02145.hp1 NA18982.hp1 NA18994.hp1 others(1): Show |
a0001 | a0001c0005a0001c0006a0001c0021others(1): Show | a0001c0005t0001a0001c0006t0001a0001c0021t0002others(1): Show | a0001c0005t0001g0325a0001c0006t0001g0264a0001c0021t0002g0321others(1): Show | 4 | 363 | 0.0110 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1888566 | CACTG | C | intron_variant | MODIFIER | HG00621.hp2 NA18941.hp2 NA18943.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0010 | a0001c0001t0002a0001c0001t0004a0001c0002t0001others(2): Show | a0001c0001t0002g0224a0001c0001t0002g0271a0001c0001t0004g0141others(5): Show | 8 | 363 | 0.0220 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1888583 | GGGGT | G | intron_variant | MODIFIER | HG00621.hp2 NA18941.hp2 NA18943.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0010 | a0001c0001t0002a0001c0001t0004a0001c0002t0001others(2): Show | a0001c0001t0002g0224a0001c0001t0002g0271a0001c0001t0004g0141others(5): Show | 8 | 363 | 0.0220 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1888721 | AATAG | A | intron_variant | MODIFIER | NA18941.hp2 NA18943.hp2 NA18966.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0010 | a0001c0001t0002a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0002g0271a0001c0002t0001g0270a0001c0002t0002g0002others(3): Show | 6 | 363 | 0.0165 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1888749 | GAATA | G | intron_variant | MODIFIER | NA18941.hp2 NA18943.hp2 NA18966.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0010 | a0001c0001t0002a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0002g0271a0001c0002t0001g0270a0001c0002t0002g0002others(3): Show | 6 | 363 | 0.0165 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1888750 | AATAG | A | intron_variant | MODIFIER | HG00642.hp1 HG00738.hp2 HG01255.hp1 others(5): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0019a0001c0002t0001a0001c0002t0010others(5): Show | a0001c0001t0019g0278a0001c0002t0001g0037a0001c0002t0010g0212others(5): Show | 8 | 363 | 0.0220 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1888774 | CACTG | C | intron_variant | MODIFIER | HG00642.hp1 HG00673.hp1 HG00738.hp2 others(20): Show |
a0001a0004a0006 | a0001c0001a0001c0002a0001c0003others(15): Show | a0001c0001t0019a0001c0002t0001a0001c0002t0010others(19): Show | a0001c0001t0019g0278a0001c0002t0001g0037a0001c0002t0010g0212others(20): Show | 23 | 363 | 0.0634 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1888779 | AGTGG | A | intron_variant | MODIFIER | HG02280.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
a0001a0004 | a0001c0002a0001c0007a0001c0012others(2): Show | a0001c0002t0001a0001c0002t0003a0001c0007t0003others(3): Show | a0001c0002t0001g0211a0001c0002t0001g0267a0001c0002t0003g0348others(5): Show | 8 | 363 | 0.0220 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1888803 | CACTG | C | intron_variant | MODIFIER | HG00741.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
a0001a0004a0011others(2): Show | a0001c0001a0001c0002a0001c0005others(7): Show | a0001c0001t0004a0001c0001t0014a0001c0001t0019others(10): Show | a0001c0001t0004g0354a0001c0001t0014g0361a0001c0001t0019g0320others(12): Show | 15 | 363 | 0.0413 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1888861 | CACTG | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(69): Show |
a0001a0002a0005others(6): Show | a0001c0001a0001c0002a0001c0003others(48): Show | a0001c0001t0002a0001c0001t0004a0001c0002t0001others(58): Show | a0001c0001t0002g0224a0001c0001t0004g0141a0001c0001t0004g0165others(68): Show | 72 | 363 | 0.1984 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1888962 | GGGTC | G | intron_variant | MODIFIER | HG00642.hp1 HG00738.hp2 HG01346.hp1 others(4): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0019a0001c0002t0001a0001c0002t0010others(4): Show | a0001c0001t0019g0278a0001c0002t0001g0037a0001c0002t0010g0212others(4): Show | 7 | 363 | 0.0193 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1889012 | GTGCA | G | intron_variant | MODIFIER | NA18941.hp2 NA18943.hp2 NA18966.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0010 | a0001c0001t0002a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0002g0271a0001c0002t0001g0270a0001c0002t0002g0002others(3): Show | 6 | 363 | 0.0165 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1889035 | CATGG | C | intron_variant | MODIFIER | NA18941.hp2 NA18943.hp2 NA18966.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0010 | a0001c0001t0002a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0002g0271a0001c0002t0001g0270a0001c0002t0002g0002others(3): Show | 6 | 363 | 0.0165 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1889107 | TGTGA | T | intron_variant | MODIFIER | HG00642.hp1 HG00738.hp2 HG01346.hp1 others(5): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0019a0001c0002t0001a0001c0002t0010others(5): Show | a0001c0001t0019g0278a0001c0002t0001g0037a0001c0002t0010g0212others(5): Show | 8 | 363 | 0.0220 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1889215 | AATGG | A | intron_variant | MODIFIER | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(15): Show |
a0002a0014a0018 | a0002c0025a0002c0028a0002c0032others(14): Show | a0002c0025t0059a0002c0028t0001a0002c0032t0004others(14): Show | a0002c0025t0059g0105a0002c0028t0001g0223a0002c0032t0004g0173others(15): Show | 18 | 363 | 0.0496 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1889239 | CATTG | C | intron_variant | MODIFIER | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(27): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0002a0001c0003others(23): Show | a0001c0001t0019a0001c0002t0001a0001c0002t0010others(24): Show | a0001c0001t0019g0278a0001c0002t0001g0037a0001c0002t0001g0259others(27): Show | 30 | 363 | 0.0826 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1889299 | ACTGC | A | intron_variant | MODIFIER | HG01975.hp2 HG03669.hp1 HG06807.hp1 |
a0001a0002a0004 | a0001c0009a0002c0025a0004c0040 | a0001c0009t0069a0002c0025t0024a0004c0040t0065 | a0001c0009t0069g0302a0002c0025t0024g0106a0004c0040t0065g0181 | 3 | 363 | 0.0083 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1889398 | GCATC | G | intron_variant | MODIFIER | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(15): Show |
a0002a0014a0018 | a0002c0025a0002c0028a0002c0032others(14): Show | a0002c0025t0059a0002c0028t0001a0002c0032t0004others(14): Show | a0002c0025t0059g0105a0002c0028t0001g0223a0002c0032t0004g0173others(15): Show | 18 | 363 | 0.0496 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1889475 | CACTG | C | intron_variant | MODIFIER | HG00621.hp2 HG00642.hp1 HG00738.hp2 others(20): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(17): Show | a0001c0001t0002g0224a0001c0001t0004g0141a0001c0001t0006g0115others(20): Show | 23 | 363 | 0.0634 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1889506 | CACTG | C | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(21): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0002a0001c0003others(14): Show | a0001c0001t0002a0001c0002t0001a0001c0002t0002others(17): Show | a0001c0001t0002g0271a0001c0002t0001g0198a0001c0002t0001g0270others(21): Show | 24 | 363 | 0.0661 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1889567 | CACTG | C | intron_variant | MODIFIER | HG00642.hp1 HG00738.hp2 HG01346.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0002a0001c0001t0019a0001c0002t0001others(4): Show | a0001c0001t0002g0271a0001c0001t0019g0278a0001c0002t0001g0037others(6): Show | 9 | 363 | 0.0248 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1889630 | CATGG | C | intron_variant | MODIFIER | HG00423.hp1 HG00544.hp1 HG00621.hp1 others(15): Show |
a0002a0014a0018 | a0002c0025a0002c0028a0002c0032others(14): Show | a0002c0025t0059a0002c0028t0001a0002c0032t0004others(14): Show | a0002c0025t0059g0105a0002c0028t0001g0223a0002c0032t0004g0173others(15): Show | 18 | 363 | 0.0496 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1889659 | CTCGG | C | intron_variant | MODIFIER | HG00642.hp1 HG00738.hp2 HG01346.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0002a0001c0001t0019a0001c0002t0001others(4): Show | a0001c0001t0002g0271a0001c0001t0019g0278a0001c0002t0001g0037others(6): Show | 9 | 363 | 0.0248 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1889743 | CATTG | C | intron_variant | MODIFIER | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0001c0003others(48): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0019others(61): Show | a0001c0001t0002g0224a0001c0001t0002g0271a0001c0001t0004g0141others(74): Show | 78 | 363 | 0.2149 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1892277 | CTGTG | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(109): Show |
a0001a0002a0004others(7): Show | a0001c0001a0001c0002a0001c0003others(62): Show | a0001c0001t0002a0001c0001t0012a0001c0002t0001others(84): Show | a0001c0001t0002g0053a0001c0001t0012g0207a0001c0002t0001g0050others(108): Show | 112 | 363 | 0.3085 | -4 | c.118 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1918460 | CTGTG | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(135): Show |
a0001a0002a0003others(13): Show | a0001c0001a0001c0002a0001c0003others(68): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(97): Show | a0001c0001t0002g0066a0001c0001t0002g0069a0001c0001t0002g0232others(135): Show | 138 | 363 | 0.3802 | -4 | c.214 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1950730 | GTTTT | G | intron_variant | MODIFIER | HG01168.hp2 HG01169.hp1 HG01515.hp2 others(3): Show |
a0001a0002 | a0001c0001a0001c0009a0002c0048 | a0001c0001t0002a0001c0009t0023a0001c0009t0058others(1): Show | a0001c0001t0002g0030a0001c0001t0002g0232a0001c0001t0002g0233others(3): Show | 6 | 363 | 0.0165 | -4 | c.339 others(23): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 156944448 | CCATT | C | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(166): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0005a0001c0011others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(19): Show | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(166): Show | 169 | 362 | 0.4669 | -4 | c.299 others(19): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 30/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156979361 | CTTTT | C | intron_variant | MODIFIER | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(12): Show |
a0002 | a0002c0004 | a0002c0004t0005a0002c0004t0009a0002c0004t0025 | a0002c0004t0005g0111a0002c0004t0005g0113a0002c0004t0005g0117others(11): Show | 15 | 362 | 0.0414 | -4 | c.274 others(17): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156980833 | CGGGG | C | intron_variant | MODIFIER | HG00408.hp2 HG00642.hp1 HG01257.hp2 others(18): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0006a0002c0004t0005a0002c0004t0009others(1): Show | a0001c0001t0006g0112a0001c0001t0006g0122a0001c0001t0006g0123others(17): Show | 21 | 362 | 0.0580 | -4 | c.224 others(19): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 3/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157008406 | GCACA | G | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0011a0002c0002others(9): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(29): Show | a0001c0001t0001g0278a0001c0001t0003g0210a0001c0001t0003g0211others(158): Show | 162 | 362 | 0.4475 | -4 | c.33- others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157016798 | ATTAT | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0005a0002c0002others(10): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(42): Show | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274others(313): Show | 318 | 362 | 0.8785 | -4 | c.32+ others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157022317 | AAGTC | A | intron_variant | MODIFIER | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
a0002a0003 | a0002c0004a0003c0003 | a0002c0004t0018a0003c0003t0003 | a0002c0004t0018g0246a0002c0004t0018g0249a0002c0004t0018g0250others(4): Show | 7 | 362 | 0.0193 | -4 | c.32+ others(21): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157036126 | AAAAT | A | intron_variant | MODIFIER | HG02258.hp1 HG02896.hp2 NA19030.hp1 |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0004a0002c0004t0022 | a0001c0001t0004g0130a0002c0004t0022g0131a0002c0004t0022g0132 | 3 | 362 | 0.0083 | -4 | c.32+ others(19): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157036148 | AATAC | A | intron_variant | MODIFIER | NA18952.hp1 NA18968.hp1 NA19004.hp2 |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0017 | a0002c0002t0002g0092a0002c0002t0017g0091a0002c0002t0017g0093 | 3 | 362 | 0.0083 | -4 | c.32+ others(19): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157046899 | TACTC | T | upstream_gene_variant | MODIFIER | HG02572.hp2 HG02622.hp2 HG02976.hp1 others(1): Show |
a0002a0003 | a0002c0004a0003c0003 | a0002c0004t0005a0003c0003t0019 | a0002c0004t0005g0009a0003c0003t0019g0358a0003c0003t0019g0359others(1): Show | 4 | 362 | 0.0111 | -4 | c.-25 others(15): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1158 | chr1 | TogoVar |