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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP26_chr5_142765377_143234007 | 142778959 | TAGTG | T | intron_variant | MODIFIER | HG00438.hp1 HG02615.hp2 HG03209.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0020others(3): Show | a0001c0001t0002g0117a0001c0001t0003g0191a0001c0001t0020g0049others(3): Show | 6 | 198 | 0.0303 | -4 | c.154 others(21): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142796054 | CTGTG | C | intron_variant | MODIFIER | HG02109.hp2 HG02257.hp1 HG02622.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(8): Show | a0001c0001t0001g0029a0001c0001t0002g0008a0001c0001t0005g0101others(9): Show | 12 | 198 | 0.0606 | -4 | c.154 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142806473 | ATGTG | A | intron_variant | MODIFIER | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(36): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(24): Show | a0001c0001t0001g0141a0001c0001t0002g0023a0001c0001t0002g0142others(36): Show | 39 | 198 | 0.1970 | -4 | c.154 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142808236 | GAAAA | G | intron_variant | MODIFIER | HG00323.hp1 HG00408.hp2 HG01192.hp2 others(21): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0018others(15): Show | a0001c0001t0002g0005a0001c0001t0002g0118a0001c0001t0002g0121others(21): Show | 24 | 198 | 0.1212 | -4 | c.154 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142821300 | GTTTT | G | intron_variant | MODIFIER | HG00438.hp2 HG00558.hp1 HG01243.hp2 others(16): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0116a0001c0001t0002g0005a0001c0001t0002g0006others(16): Show | 19 | 198 | 0.0960 | -4 | c.154 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142858092 | TGTGA | T | intron_variant | MODIFIER | HG00323.hp1 HG00438.hp1 HG00544.hp1 others(12): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(7): Show | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0007others(12): Show | 15 | 198 | 0.0758 | -4 | c.155 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142867288 | GGTGT | G | intron_variant | MODIFIER | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(37): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(26): Show | a0001c0001t0001g0020a0001c0001t0001g0141a0001c0001t0002g0023others(37): Show | 40 | 198 | 0.2020 | -4 | c.155 others(21): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142880720 | TCTTA | T | intron_variant | MODIFIER | HG00558.hp1 HG01167.hp1 HG01934.hp1 others(30): Show |
a0001 | a0001c0001a0001c0003a0001c0008others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0018a0001c0001t0001g0116a0001c0001t0001g0158others(30): Show | 33 | 198 | 0.1667 | -4 | c.384 others(21): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142936108 | AACAC | A | intron_variant | MODIFIER | HG01175.hp2 HG01192.hp1 HG02523.hp1 others(11): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0003a0001c0001t0005a0001c0001t0010others(7): Show | a0001c0001t0003g0119a0001c0001t0005g0101a0001c0001t0005g0108others(11): Show | 14 | 198 | 0.0707 | -4 | c.110 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142963219 | TGCGC | T | intron_variant | MODIFIER | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(39): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | a0001c0001t0001g0012a0001c0001t0001g0153a0001c0001t0001g0196others(39): Show | 42 | 198 | 0.2121 | -4 | c.110 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142964543 | AACAC | A | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01175.hp2 others(22): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0034a0001c0001t0002g0117a0001c0001t0003g0033others(22): Show | 25 | 198 | 0.1263 | -4 | c.110 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143003784 | ATTAC | A | intron_variant | MODIFIER | HG02572.hp2 HG02818.hp2 HG03098.hp2 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0009a0001c0001t0011 | a0001c0001t0004g0002a0001c0001t0009g0039a0001c0001t0011g0094 | 3 | 198 | 0.0152 | -4 | c.110 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143007819 | TTTGA | T | intron_variant | MODIFIER | HG00323.hp1 HG00738.hp1 HG01069.hp1 others(52): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(26): Show | a0001c0001t0002g0023a0001c0001t0002g0027a0001c0001t0003g0165others(52): Show | 55 | 198 | 0.2778 | -4 | c.110 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143029392 | GTTTT | G | intron_variant | MODIFIER | HG01167.hp1 HG01934.hp1 HG02258.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(4): Show | a0001c0001t0002g0126a0001c0001t0004g0111a0001c0001t0006g0088others(4): Show | 7 | 198 | 0.0354 | -4 | c.114 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143038684 | CTTTT | C | intron_variant | MODIFIER | HG00408.hp2 HG00609.hp2 HG01175.hp1 others(21): Show |
a0001 | a0001c0001a0001c0002a0001c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0196a0001c0001t0002g0005a0001c0001t0002g0118others(21): Show | 24 | 198 | 0.1212 | -4 | c.121 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143045429 | CCCTT | C | intron_variant | MODIFIER | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(93): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0008others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(38): Show | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0029others(93): Show | 96 | 198 | 0.4849 | -4 | c.128 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 14/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143060920 | TAGAA | T | intron_variant | MODIFIER | HG02572.hp1 HG03453.hp1 |
a0001 | a0001c0001a0001c0008 | a0001c0001t0027a0001c0008t0020 | a0001c0001t0027g0097a0001c0008t0020g0177 | 2 | 198 | 0.0101 | -4 | c.153 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143104906 | CATTT | C | intron_variant | MODIFIER | HG02809.hp1 HG03139.hp2 HG03471.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0006a0001c0001t0022a0001c0002t0004others(1): Show | a0001c0001t0006g0084a0001c0001t0022g0073a0001c0002t0004g0100others(1): Show | 4 | 198 | 0.0202 | -4 | c.153 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143105378 | AAAAT | A | intron_variant | MODIFIER | HG00597.hp1 HG01069.hp2 HG01071.hp2 others(18): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(15): Show | a0001c0001t0001g0029a0001c0001t0002g0022a0001c0001t0004g0002others(18): Show | 21 | 198 | 0.1061 | -4 | c.153 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143115358 | CGAAA | C | intron_variant | MODIFIER | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(92): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0020others(92): Show | 95 | 198 | 0.4798 | -4 | c.153 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143157172 | CTTTT | C | intron_variant | MODIFIER | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(60): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0116others(60): Show | 63 | 198 | 0.3182 | -4 | c.198 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143158874 | CACAA | C | intron_variant | MODIFIER | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(45): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | a0001c0001t0001g0018a0001c0001t0001g0116a0001c0001t0001g0131others(45): Show | 48 | 198 | 0.2424 | -4 | c.198 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143163432 | GGTTT | G | intron_variant | MODIFIER | HG00408.hp2 HG01243.hp1 HG02109.hp1 others(22): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(14): Show | a0001c0001t0002g0005a0001c0001t0002g0006a0001c0001t0002g0036others(22): Show | 25 | 198 | 0.1263 | -4 | c.198 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143163461 | GTTTT | G | intron_variant | MODIFIER | HG02074.hp2 NA18950.hp2 NA18972.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0005a0001c0002t0001others(2): Show | a0001c0001t0001g0138a0001c0001t0001g0158a0001c0001t0005g0066others(3): Show | 6 | 198 | 0.0303 | -4 | c.198 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143167482 | CAAAA | C | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01243.hp2 others(13): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(9): Show | a0001c0001t0001g0012a0001c0001t0001g0034a0001c0001t0002g0117others(13): Show | 16 | 198 | 0.0808 | -4 | c.198 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143189586 | ATAAT | A | intron_variant | MODIFIER | HG00408.hp2 HG00597.hp1 HG01069.hp2 others(36): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0138a0001c0001t0001g0158a0001c0001t0002g0005others(36): Show | 39 | 198 | 0.1970 | -4 | c.198 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143193240 | CTTTT | C | intron_variant | MODIFIER | HG00323.hp2 HG01243.hp2 HG02970.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0006 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(3): Show | a0001c0001t0001g0034a0001c0001t0003g0165a0001c0001t0006g0064others(4): Show | 7 | 198 | 0.0354 | -4 | c.198 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143196955 | TAATG | T | intron_variant | MODIFIER | HG02615.hp2 HG02922.hp2 |
a0001 | a0001c0001 | a0001c0001t0013a0001c0001t0020 | a0001c0001t0013g0065a0001c0001t0020g0049 | 2 | 198 | 0.0101 | -4 | c.198 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143221923 | TGGAA | T | intron_variant | MODIFIER | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(60): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0010others(18): Show | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(60): Show | 63 | 198 | 0.3182 | -4 | c.219 others(21): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143222246 | TACAC | T | intron_variant | MODIFIER | HG00597.hp2 HG01071.hp1 HG01433.hp1 others(15): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0003a0001c0001t0014a0001c0001t0016others(6): Show | a0001c0001t0003g0019a0001c0001t0003g0119a0001c0001t0003g0143others(15): Show | 18 | 198 | 0.0909 | -4 | c.219 others(19): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143226485 | GAAAA | G | 3_prime_UTR_variant | MODIFIER | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(70): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0010others(25): Show | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0006others(70): Show | 73 | 198 | 0.3687 | -4 | c.*40 others(15): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 23/23 | 4057 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||
ARHGAP26_chr5_142765377_143234007 | 143231607 | GGGTT | G | downstream_gene_variant | MODIFIER | HG03098.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0014a0001c0001t0023a0001c0002t0049 | a0001c0001t0014g0038a0001c0001t0014g0041a0001c0001t0023g0055others(1): Show | 4 | 198 | 0.0202 | -4 | c.*91 others(15): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 2601 | chr5 | TogoVar | ||||||
ARHGAP27_chr17_45388908_45437870 | 45390086 | CTGAG | C | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00609.hp2 others(132): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0016a0002c0002others(9): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(19): Show | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(131): Show | 135 | 347 | 0.3891 | -4 | c.*53 others(15): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 3821 | chr17 | TogoVar | ||||||
ARHGAP27_chr17_45388908_45437870 | 45419512 | GTATA | G | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG01071.hp2 others(36): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0016a0002c0002others(2): Show | a0001c0001t0006a0001c0001t0010a0001c0001t0021others(9): Show | a0001c0001t0006g0009a0001c0001t0006g0022a0001c0001t0010g0019others(35): Show | 39 | 347 | 0.1124 | -4 | c.657 others(23): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6729499 | CACAG | C | upstream_gene_variant | MODIFIER | HG01243.hp2 HG02818.hp1 HG03471.hp2 |
a0001a0008 | a0001c0001a0001c0003a0008c0011 | a0001c0001t0001a0001c0003t0003a0008c0011t0005 | a0001c0001t0001g0151a0001c0003t0003g0154a0008c0011t0005g0152 | 3 | 248 | 0.0121 | -4 | c.-32 others(13): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 216 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6730171 | TAGCA | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0003a0001c0010others(17): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(30): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0019others(133): Show | 136 | 248 | 0.5484 | -4 | c.122 others(19): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6731291 | CGTGT | C | intron_variant | MODIFIER | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(4): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0019others(1): Show | a0001c0001t0007a0001c0001t0022a0001c0003t0003others(2): Show | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0022g0067others(4): Show | 7 | 248 | 0.0282 | -4 | c.122 others(21): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6775513 | TTTTG | T | intron_variant | MODIFIER | HG01884.hp2 HG01952.hp2 HG02145.hp2 others(6): Show |
a0001a0002a0006others(1): Show | a0001c0001a0001c0003a0001c0012others(3): Show | a0001c0001t0001a0001c0001t0006a0001c0003t0003others(5): Show | a0001c0001t0001g0106a0001c0001t0001g0161a0001c0001t0006g0164others(6): Show | 9 | 248 | 0.0363 | -4 | c.122 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6810778 | TAAAG | T | intron_variant | MODIFIER | HG02559.hp2 HG02647.hp1 HG02723.hp1 |
a0001 | a0001c0001a0001c0003a0001c0012 | a0001c0001t0001a0001c0003t0003a0001c0012t0014 | a0001c0001t0001g0106a0001c0003t0003g0122a0001c0012t0014g0159 | 3 | 248 | 0.0121 | -4 | c.123 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6830282 | CTCTT | C | intron_variant | MODIFIER | HG01106.hp1 HG03471.hp1 NA18940.hp1 others(2): Show |
a0001a0010 | a0001c0001a0001c0003a0010c0014 | a0001c0001t0001a0001c0003t0003a0010c0014t0001 | a0001c0001t0001g0205a0001c0003t0003g0002a0001c0003t0003g0085others(2): Show | 5 | 248 | 0.0202 | -4 | c.325 others(21): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6841180 | CCTCT | C | intron_variant | MODIFIER | HG00558.hp1 HG03942.hp1 NA19063.hp1 others(2): Show |
a0001a0003a0004 | a0001c0003a0003c0004a0004c0007 | a0001c0003t0003a0003c0004t0001a0004c0007t0002 | a0001c0003t0003g0208a0003c0004t0001g0020a0003c0004t0001g0136others(2): Show | 5 | 248 | 0.0202 | -4 | c.543 others(21): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6841203 | CCTCT | C | intron_variant | MODIFIER | HG00140.hp2 HG00544.hp2 HG02135.hp1 others(10): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0002c0005others(2): Show | a0001c0001t0001a0001c0001t0017a0002c0002t0002others(4): Show | a0001c0001t0001g0029a0001c0001t0001g0188a0001c0001t0017g0118others(10): Show | 13 | 248 | 0.0524 | -4 | c.543 others(21): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6841208 | CCTCT | C | intron_variant | MODIFIER | HG00558.hp1 HG01884.hp2 HG02145.hp1 others(7): Show |
a0001a0003a0004others(1): Show | a0001c0001a0003c0004a0004c0007others(1): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(3): Show | a0001c0001t0001g0124a0001c0001t0001g0149a0001c0001t0001g0150others(7): Show | 10 | 248 | 0.0403 | -4 | c.543 others(21): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6892032 | TCTGA | T | intron_variant | MODIFIER | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
a0003 | a0003c0013a0003c0023 | a0003c0013t0011a0003c0023t0001 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120 | 3 | 248 | 0.0121 | -4 | c.184 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6901540 | TAAAA | T | intron_variant | MODIFIER | HG01081.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
a0001a0003 | a0001c0010a0003c0013a0003c0023 | a0001c0010t0003a0003c0013t0011a0003c0023t0001 | a0001c0010t0003g0089a0001c0010t0003g0098a0001c0010t0003g0114others(3): Show | 6 | 248 | 0.0242 | -4 | c.203 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6910847 | GCTTT | G | intron_variant | MODIFIER | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(3): Show |
a0001a0003 | a0001c0001a0003c0013a0003c0023 | a0001c0001t0007a0003c0013t0011a0003c0023t0001 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212others(3): Show | 6 | 248 | 0.0242 | -4 | c.209 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6915542 | CAACT | C | 3_prime_UTR_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
a0001a0003a0005others(4): Show | a0001c0001a0001c0003a0001c0010others(15): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(28): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(180): Show | 183 | 248 | 0.7379 | -4 | c.*33 others(15): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 18/18 | 3390 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||
ARHGAP29_chr1_94163905_94242584 | 94167597 | AAAAC | A | downstream_gene_variant | MODIFIER | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0010a0001c0001t0041 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(4): Show | 8 | 356 | 0.0225 | -4 | c.*62 others(15): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 1307 | chr1 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94198184 | CAATT | C | intron_variant | MODIFIER | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
a0001a0007a0008 | a0001c0001a0001c0012a0007c0013others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(17): Show | a0001c0001t0002g0003a0001c0001t0002g0026a0001c0001t0002g0027others(112): Show | 132 | 356 | 0.3708 | -4 | c.128 others(23): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161053462 | TTCTC | T | intron_variant | MODIFIER | HG01168.hp2 HG01175.hp1 HG01255.hp2 others(24): Show |
a0001a0002a0005 | a0001c0001a0001c0014a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(4): Show | a0001c0001t0001g0010a0001c0001t0001g0027a0001c0001t0001g0044others(24): Show | 27 | 390 | 0.0692 | -4 | c.537 others(17): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 5/11 | chr1 | TogoVar |