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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP15_chr2_143124419_143773352 | 143346250 | TCACA | T | intron_variant | MODIFIER | HG00738.hp2 HG01071.hp2 HG01256.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0021 a0001c0001t0001g0136 a0001c0001t0001g0156 |
3 | 162 | 0.0185 | -4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143372011 | GAAAT | G | intron_variant | MODIFIER | HG00642.hp2 HG01069.hp2 HG01243.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0001 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(7): Show |
10 | 162 | 0.0617 | -4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143379485 | ATATG | A | intron_variant | MODIFIER | HG02523.hp1 HG02602.hp1 HG03490.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0037 a0001c0001t0001g0053 a0001c0001t0001g0068 others(6): Show |
9 | 162 | 0.0556 | -4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143379487 | ATGTG | A | intron_variant | MODIFIER | HG00733.hp1 HG01255.hp1 HG01361.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0001c0002t0001g0043 others(2): Show |
5 | 162 | 0.0309 | -4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143387942 | TACAC | T | intron_variant | MODIFIER | HG01243.hp2 HG02109.hp2 HG02559.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007 a0001c0001t0001g0062 a0001c0001t0001g0099 others(3): Show |
6 | 162 | 0.0370 | -4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143390731 | GCACA | G | intron_variant | MODIFIER | HG00733.hp2 HG01081.hp1 HG01256.hp2 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0040 others(14): Show |
17 | 162 | 0.1049 | -4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143397316 | ATGTG | A | intron_variant | MODIFIER | HG02145.hp2 NA18906.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0128 a0001c0001t0001g0135 |
2 | 162 | 0.0124 | -4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143397344 | GTGTA | G | intron_variant | MODIFIER | HG00621.hp2 HG00738.hp1 HG00741.hp2 others(21): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0031 others(21): Show |
24 | 162 | 0.1482 | -4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143397903 | CAAAG | C | intron_variant | MODIFIER | HG02109.hp2 HG02559.hp1 HG02976.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
4 | 162 | 0.0247 | -4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143405242 | CAAAT | C | intron_variant | MODIFIER | HG02559.hp2 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0061 a0001c0001t0001g0091 |
2 | 162 | 0.0124 | -4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143407987 | GTATA | G | intron_variant | MODIFIER | HG01255.hp1 HG02071.hp1 HG02280.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0030 others(5): Show |
8 | 162 | 0.0494 | -4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143411427 | AAAAC | A | intron_variant | MODIFIER | HG00741.hp1 HG01081.hp2 HG02602.hp1 others(4): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0002 | a0001c0002t0001g0012 a0001c0002t0001g0036 a0001c0002t0001g0065 others(4): Show |
7 | 162 | 0.0432 | -4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143416263 | AAAAC | A | intron_variant | MODIFIER | HG00609.hp1 HG01358.hp2 HG02071.hp2 others(19): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0032 others(19): Show |
22 | 162 | 0.1358 | -4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143421766 | GTATA | G | intron_variant | MODIFIER | HG03139.hp1 HG06807.hp2 NA18955.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 a0001c0001t0001g0034 a0001c0001t0001g0124 |
3 | 162 | 0.0185 | -4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143425341 | TTATA | T | intron_variant | MODIFIER | HG02145.hp1 HG03225.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041 a0001c0001t0001g0137 |
2 | 162 | 0.0124 | -4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143433766 | GTTTA | G | intron_variant | MODIFIER | HG02486.hp1 HG02809.hp1 HG02976.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0027 a0001c0001t0001g0057 a0001c0001t0001g0088 others(1): Show |
4 | 162 | 0.0247 | -4 | c.475 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143468633 | TGAGA | T | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG00738.hp1 others(59): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0013 others(59): Show |
62 | 162 | 0.3827 | -4 | c.704 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143471007 | TAAAG | T | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(19): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 a0001c0001t0001g0014 a0001c0001t0001g0017 others(19): Show |
22 | 162 | 0.1358 | -4 | c.704 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143477190 | GCACA | G | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG01243.hp2 others(29): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0015 others(29): Show |
32 | 162 | 0.1975 | -4 | c.704 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143535380 | TTTAA | T | intron_variant | MODIFIER | HG02071.hp1 NA18747.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0024 a0001c0001t0001g0028 |
2 | 162 | 0.0124 | -4 | c.925 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143573462 | TAAAG | T | intron_variant | MODIFIER | HG00609.hp2 HG00621.hp1 HG00738.hp1 others(45): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0005 | a0001c0001t0001a0001c0002t0001a0003c0005t0001 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(45): Show |
48 | 162 | 0.2963 | -4 | c.100 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143610719 | GTATT | G | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(59): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(59): Show |
62 | 162 | 0.3827 | -4 | c.100 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143613154 | TTAAG | T | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(50): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(50): Show |
53 | 162 | 0.3272 | -4 | c.100 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143621380 | GGTTA | G | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(17): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0068 others(17): Show |
20 | 162 | 0.1235 | -4 | c.100 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143622781 | TAAAA | T | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG00741.hp1 others(64): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(64): Show |
67 | 162 | 0.4136 | -4 | c.100 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143638657 | AAAAT | A | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(54): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0005 | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(54): Show |
57 | 162 | 0.3519 | -4 | c.113 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143643045 | TTAAC | T | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(14): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0068 others(14): Show |
17 | 162 | 0.1049 | -4 | c.113 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143656934 | GGTGT | G | intron_variant | MODIFIER | HG00621.hp1 HG01243.hp1 HG02145.hp1 others(17): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(17): Show |
20 | 162 | 0.1235 | -4 | c.113 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143679646 | CGTGT | C | intron_variant | MODIFIER | HG02109.hp1 HG03139.hp2 HG03831.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0100 others(2): Show |
5 | 162 | 0.0309 | -4 | c.113 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143686383 | CAAAA | C | intron_variant | MODIFIER | HG00621.hp2 HG00642.hp1 HG01255.hp1 others(16): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(16): Show |
19 | 162 | 0.1173 | -4 | c.113 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143696179 | GAAGA | G | intron_variant | MODIFIER | HG01261.hp1 HG02809.hp1 HG02809.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 a0001c0001t0001g0039 a0001c0001t0001g0049 others(4): Show |
7 | 162 | 0.0432 | -4 | c.113 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143701800 | CTCTT | C | intron_variant | MODIFIER | HG00621.hp2 HG00642.hp1 HG01071.hp2 others(25): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0003t0001 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(25): Show |
28 | 162 | 0.1728 | -4 | c.113 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143727455 | TTTTG | T | intron_variant | MODIFIER | HG00642.hp2 HG01069.hp2 HG01255.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0029 a0001c0001t0001g0068 a0001c0001t0001g0081 others(10): Show |
13 | 162 | 0.0803 | -4 | c.124 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143730400 | ATTTC | A | intron_variant | MODIFIER | HG00621.hp1 HG00733.hp1 HG00733.hp2 others(30): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0016 others(30): Show |
33 | 162 | 0.2037 | -4 | c.124 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143737726 | TTTTA | T | intron_variant | MODIFIER | HG00621.hp1 HG00733.hp2 HG01081.hp1 others(36): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0001 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(36): Show |
39 | 162 | 0.2407 | -4 | c.124 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143761513 | AAAAG | A | intron_variant | MODIFIER | HG00642.hp2 HG01069.hp2 HG01255.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0109 others(9): Show |
12 | 162 | 0.0741 | -4 | c.124 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143765109 | ATGTG | A | intron_variant | MODIFIER | HG00738.hp2 HG01243.hp2 HG02145.hp1 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(14): Show |
17 | 162 | 0.1049 | -4 | c.124 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24916423 | CTTTT | C | downstream_gene_variant | MODIFIER | HG00323.hp2 HG01069.hp2 HG01074.hp2 others(22): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0014 others(20): Show |
25 | 240 | 0.1042 | -4 | c.*37 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2965 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24916596 | TACAC | T | downstream_gene_variant | MODIFIER | HG00323.hp2 HG01099.hp1 HG01243.hp2 others(7): Show |
a0001a0003 | a0001c0001a0003c0006 | a0001c0001t0001a0003c0006t0001 | a0001c0001t0001g0001 a0001c0001t0001g0055 a0001c0001t0001g0076 others(7): Show |
10 | 240 | 0.0417 | -4 | c.*35 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2792 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24916626 | CACAT | C | downstream_gene_variant | MODIFIER | HG01496.hp1 HG01884.hp2 HG02145.hp1 others(4): Show |
a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0210 a0001c0003t0003g0211 a0001c0003t0003g0214 others(4): Show |
7 | 240 | 0.0292 | -4 | c.*35 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2762 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24916816 | GCGCA | G | downstream_gene_variant | MODIFIER | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(5): Show |
a0001 | a0001c0004 | a0001c0004t0002a0001c0004t0008 | a0001c0004t0002g0103 a0001c0004t0002g0108 a0001c0004t0002g0110 others(5): Show |
8 | 240 | 0.0333 | -4 | c.*33 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2572 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24916818 | GCACA | G | downstream_gene_variant | MODIFIER | HG01978.hp2 HG02523.hp2 HG04199.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0050 a0001c0001t0001g0164 a0001c0001t0001g0184 others(3): Show |
6 | 240 | 0.0250 | -4 | c.*33 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2570 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24917332 | CCTCT | C | downstream_gene_variant | MODIFIER | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0002a0001c0004t0002a0001c0004t0008 | a0001c0001t0002g0031 a0001c0004t0002g0103 a0001c0004t0002g0108 others(6): Show |
9 | 240 | 0.0375 | -4 | c.*27 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2056 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24926118 | AAAAG | A | intron_variant | MODIFIER | HG01934.hp1 HG02258.hp1 HG02258.hp2 others(9): Show |
a0001a0002 | a0001c0001a0002c0008 | a0001c0001t0001a0002c0008t0001 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(9): Show |
12 | 240 | 0.0500 | -4 | c.251 others(23): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 19/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24933254 | TCTGA | T | intron_variant | MODIFIER | HG01167.hp1 HG01934.hp1 HG02109.hp2 others(30): Show |
a0001a0002 | a0001c0001a0002c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0020 others(29): Show |
33 | 240 | 0.1375 | -4 | c.189 others(23): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 18/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24938937 | GAATC | G | intron_variant | MODIFIER | HG01934.hp1 HG02109.hp1 HG02109.hp2 others(21): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0007 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0020 others(20): Show |
24 | 240 | 0.1000 | -4 | c.172 others(21): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 17/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24961911 | TTATA | T | intron_variant | MODIFIER | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(11): Show |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0005a0001c0003t0003a0001c0005t0001 | a0001c0001t0005g0003 a0001c0001t0005g0230 a0001c0001t0005g0231 others(10): Show |
14 | 240 | 0.0583 | -4 | c.574 others(21): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 24985188 | CCACA | C | intron_variant | MODIFIER | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(120): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(8): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0017 others(115): Show |
123 | 240 | 0.5125 | -4 | c.54- others(19): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 25009364 | CAAAA | C | intron_variant | MODIFIER | HG01074.hp2 HG01099.hp2 HG01167.hp1 others(20): Show |
a0001a0002 | a0001c0001a0002c0008 | a0001c0001t0001a0001c0001t0004a0002c0008t0001 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(20): Show |
23 | 240 | 0.0958 | -4 | c.53+ others(19): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | |||||||
ARHGAP17_chr16_24914389_25020369 | 25020228 | GAAGA | G | upstream_gene_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG00642.hp2 others(18): Show |
a0001a0003 | a0001c0001a0003c0006 | a0001c0001t0001a0003c0006t0001 | a0001c0001t0001g0054 a0001c0001t0001g0086 a0001c0001t0001g0126 others(18): Show |
21 | 240 | 0.0875 | -4 | c.-49 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4860 | chr16 | TogoVar |