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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP23_chr17_38423464_38517385 | 38447437 | G | GAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0064 | 1 | 164 | 0.0061 | 10 | c.64- others(27): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38467557 | T | TTATCCTT others(3): Show |
intron_variant | MODIFIER | NA19054.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 | 1 | 305 | 0.0033 | 10 | c.164 others(27): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38480897 | C | CTGTCCCA others(3): Show |
intron_variant | MODIFIER | NA18959.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0095 | 1 | 308 | 0.0032 | 10 | c.262 others(29): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38513074 | T | TTAAATAT others(3): Show |
downstream_gene_variant | MODIFIER | HG02055.hp2 HG02886.hp1 HG03098.hp2 others(6): Show |
a0001 | a0001c0001a0001c0005a0001c0010 | a0001c0001t0001a0001c0001t0009a0001c0005t0001others(1): Show | a0001c0001t0001g0005 a0001c0001t0001g0282 a0001c0001t0009g0005 others(6): Show |
9 | 60 | 0.1500 | 10 | c.*21 others(21): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 690 | chr17 | TogoVar | |||||||
ARHGAP24_chr4_85470150_86007666 | 85485376 | A | AAAAAAAA others(3): Show |
intron_variant | MODIFIER | NA18522.hp2 | a0001 | a0001c0004 | a0001c0004t0004 | a0001c0004t0004g0036 | 1 | 64 | 0.0156 | 10 | c.-21 others(27): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85564924 | G | GTATATAT others(3): Show |
intron_variant | MODIFIER | HG00423.hp2 HG02622.hp1 HG03471.hp1 |
a0001 | a0001c0002a0001c0008a0001c0013 | a0001c0002t0008a0001c0008t0014a0001c0013t0001 | a0001c0002t0008g0052 a0001c0008t0014g0065 a0001c0013t0001g0019 |
3 | 30 | 0.1000 | 10 | c.-20 others(27): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85612083 | T | TACACACA others(3): Show |
intron_variant | MODIFIER | HG00423.hp2 HG01168.hp1 HG03130.hp1 |
a0001 | a0001c0001a0001c0002a0001c0013 | a0001c0001t0001a0001c0002t0002a0001c0013t0001 | a0001c0001t0001g0061 a0001c0002t0002g0085 a0001c0013t0001g0019 |
3 | 12 | 0.2500 | 10 | c.180 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85655766 | C | CATATATA others(3): Show |
intron_variant | MODIFIER | HG01884.hp1 HG02258.hp2 NA18522.hp2 |
a0001 | a0001c0003a0001c0004a0001c0005 | a0001c0003t0011a0001c0004t0004a0001c0005t0004 | a0001c0003t0011g0095 a0001c0004t0004g0036 a0001c0005t0004g0034 |
3 | 98 | 0.0306 | 10 | c.181 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85655792 | T | TATAGAGA others(3): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0044 | 1 | 48 | 0.0208 | 10 | c.181 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85655792 | T | TATATATA others(3): Show |
intron_variant | MODIFIER | HG01243.hp2 | a0001 | a0001c0004 | a0001c0004t0003 | a0001c0004t0003g0072 | 1 | 48 | 0.0208 | 10 | c.181 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85655810 | G | GAGAGAGA others(3): Show |
intron_variant | MODIFIER | HG01109.hp2 HG02723.hp2 HG03516.hp1 others(1): Show |
a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0001a0001c0003t0005a0001c0004t0004 | a0001c0001t0001g0030 a0001c0001t0001g0039 a0001c0003t0005g0059 others(1): Show |
4 | 101 | 0.0396 | 10 | c.181 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85655812 | G | GAGAGAGA others(3): Show |
intron_variant | MODIFIER | HG02622.hp1 | a0001 | a0001c0008 | a0001c0008t0014 | a0001c0008t0014g0065 | 1 | 83 | 0.0120 | 10 | c.181 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85655816 | G | GAGAGAGA others(3): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0048 | 1 | 103 | 0.0097 | 10 | c.181 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85660794 | C | CAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG01070.hp2 HG02055.hp1 HG02109.hp2 others(3): Show |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0001a0001c0003t0005a0001c0005t0004 | a0001c0001t0001g0032 a0001c0001t0001g0048 a0001c0001t0001g0097 others(3): Show |
6 | 9 | 0.6667 | 10 | c.181 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85733060 | C | CTTTTTTT others(3): Show |
intron_variant | MODIFIER | HG01069.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0102 | 1 | 15 | 0.0667 | 10 | c.268 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85743392 | C | CAAAAAAA others(3): Show |
intron_variant | MODIFIER | NA20300.hp2 | a0002 | a0002c0006 | a0002c0006t0006 | a0002c0006t0006g0091 | 1 | 7 | 0.1429 | 10 | c.268 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85813818 | T | TTATATAT others(3): Show |
intron_variant | MODIFIER | HG01167.hp2 HG02486.hp1 |
a0001 | a0001c0002a0001c0007 | a0001c0002t0007a0001c0007t0003 | a0001c0002t0007g0056 a0001c0007t0003g0043 |
2 | 46 | 0.0435 | 10 | c.268 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85827461 | C | CGTGTGTG others(3): Show |
intron_variant | MODIFIER | HG00735.hp2 HG04204.hp2 |
a0001a0003 | a0001c0002a0003c0012 | a0001c0002t0002a0003c0012t0001 | a0001c0002t0002g0076 a0003c0012t0001g0027 |
2 | 17 | 0.1176 | 10 | c.269 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85859212 | T | TACACACA others(3): Show |
intron_variant | MODIFIER | HG02258.hp1 HG02897.hp2 HG03471.hp1 others(2): Show |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0008 | a0001c0002t0002g0004 a0001c0002t0002g0041 a0001c0002t0002g0069 others(2): Show |
5 | 20 | 0.2500 | 10 | c.269 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85867898 | C | CATATATA others(3): Show |
intron_variant | MODIFIER | HG02615.hp1 HG02809.hp2 HG03579.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0045 a0001c0001t0001g0068 a0001c0001t0001g0104 |
3 | 48 | 0.0625 | 10 | c.269 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85973833 | G | GTTTTTTT others(3): Show |
intron_variant | MODIFIER | HG03130.hp1 HG03516.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0039 a0001c0001t0001g0061 |
2 | 33 | 0.0606 | 10 | c.733 others(27): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85997628 | G | GTTTCTAA others(3): Show |
intron_variant | MODIFIER | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(60): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0021others(23): Show | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0026 others(60): Show |
63 | 108 | 0.5833 | 10 | c.200 others(29): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142851236 | A | ACAGATGT others(3): Show |
intron_variant | MODIFIER | HG02809.hp1 HG03098.hp2 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004a0001c0001t0006 | a0001c0001t0002g0022 a0001c0001t0004g0002 a0001c0001t0006g0084 |
3 | 196 | 0.0153 | 10 | c.155 others(29): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142858061 | C | CTGTGTGT others(3): Show |
intron_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG02080.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0024a0001c0001t0032others(6): Show | a0001c0001t0001g0020 a0001c0001t0001g0153 a0001c0001t0024g0103 others(9): Show |
12 | 111 | 0.1081 | 10 | c.155 others(29): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142858094 | T | TGTGTGTG others(3): Show |
intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0024 | 1 | 154 | 0.0065 | 10 | c.155 others(29): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142867288 | G | GGTGTGTG others(3): Show |
intron_variant | MODIFIER | HG02818.hp1 NA18906.hp2 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0009 | a0001c0001t0006g0086 a0001c0001t0009g0026 |
2 | 47 | 0.0426 | 10 | c.155 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142890136 | T | TAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG02622.hp2 HG02897.hp1 NA19090.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0011 | a0001c0001t0001g0153 a0001c0001t0002g0008 a0001c0001t0011g0091 |
3 | 153 | 0.0196 | 10 | c.487 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142890151 | A | AAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG01243.hp1 NA18995.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0020a0001c0002t0003 | a0001c0001t0020g0079 a0001c0002t0003g0168 |
2 | 117 | 0.0171 | 10 | c.487 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142890151 | A | AAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG03209.hp1 NA18960.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0002t0001 | a0001c0001t0004g0099 a0001c0002t0001g0147 |
2 | 117 | 0.0171 | 10 | c.487 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142890151 | A | AAAATATA others(3): Show |
intron_variant | MODIFIER | HG02056.hp2 NA18957.hp2 NA19082.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0004t0007 | a0001c0001t0001g0017 a0001c0001t0002g0126 a0001c0004t0007g0054 |
3 | 118 | 0.0254 | 10 | c.487 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142936108 | A | AACACACA others(3): Show |
intron_variant | MODIFIER | HG00438.hp2 HG00544.hp1 HG00609.hp1 others(25): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(12): Show | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0131 others(25): Show |
28 | 102 | 0.2745 | 10 | c.110 others(29): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949200 | A | AGAGGAGA others(3): Show |
intron_variant | MODIFIER | HG02698.hp2 NA18990.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0002t0003 | a0001c0001t0003g0188 a0001c0002t0003g0140 |
2 | 182 | 0.0110 | 10 | c.110 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949202 | A | AGAGGAGA others(3): Show |
intron_variant | MODIFIER | HG00558.hp1 HG02074.hp1 HG02109.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0015others(2): Show | a0001c0001t0001g0153 a0001c0001t0002g0195 a0001c0001t0015g0123 others(2): Show |
5 | 182 | 0.0275 | 10 | c.110 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949206 | A | AGAGGAGA others(3): Show |
intron_variant | MODIFIER | HG02897.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0036 | 1 | 183 | 0.0055 | 10 | c.110 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142955095 | T | TACACACA others(3): Show |
intron_variant | MODIFIER | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(22): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0029 a0001c0001t0002g0036 a0001c0001t0002g0190 others(22): Show |
25 | 74 | 0.3378 | 10 | c.110 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142963181 | T | TATATATA others(3): Show |
intron_variant | MODIFIER | HG02897.hp2 HG03041.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0029 a0001c0001t0002g0036 |
2 | 174 | 0.0115 | 10 | c.110 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142963196 | A | ATGTGTGT others(3): Show |
intron_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0026 | 1 | 186 | 0.0054 | 10 | c.110 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATATATAT others(3): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0100 | 1 | 144 | 0.0069 | 10 | c.110 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142963204 | G | GTATATAT others(3): Show |
intron_variant | MODIFIER | NA19058.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0138 | 1 | 154 | 0.0065 | 10 | c.110 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142980352 | C | CTTTATTT others(3): Show |
intron_variant | MODIFIER | HG00438.hp2 HG00558.hp1 HG00597.hp2 others(50): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(25): Show | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0158 others(50): Show |
53 | 69 | 0.7681 | 10 | c.110 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143009928 | T | TATTGTAT others(3): Show |
intron_variant | MODIFIER | HG02258.hp1 HG02647.hp1 HG02818.hp1 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0010a0001c0001t0025 | a0001c0001t0006g0086 a0001c0001t0010g0080 a0001c0001t0025g0071 |
3 | 196 | 0.0153 | 10 | c.110 others(29): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | |||||||
ARHGAP26_chr5_142765377_143234007 | 143012552 | C | CATATATA others(3): Show |
intron_variant | MODIFIER | HG06807.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0190 | 1 | 48 | 0.0208 | 10 | c.110 others(29): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143087636 | C | CTTTTTTT others(3): Show |
intron_variant | MODIFIER | HG02074.hp2 HG03540.hp1 |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0016 | a0001c0001t0005g0066 a0001c0001t0016g0024 |
2 | 47 | 0.0426 | 10 | c.153 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143162284 | T | TACACACA others(3): Show |
intron_variant | MODIFIER | HG01934.hp1 HG02723.hp1 HG03041.hp1 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0015a0001c0001t0043 | a0001c0001t0006g0095 a0001c0001t0015g0037 a0001c0001t0043g0042 |
3 | 51 | 0.0588 | 10 | c.198 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143162314 | C | CACACACA others(3): Show |
intron_variant | MODIFIER | HG02735.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0142 | 1 | 196 | 0.0051 | 10 | c.198 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143168445 | C | CTTTTTTT others(3): Show |
intron_variant | MODIFIER | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(16): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0141 a0001c0001t0002g0013 a0001c0001t0003g0015 others(16): Show |
19 | 43 | 0.4419 | 10 | c.198 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP27_chr17_45388908_45437870 | 45399591 | C | CAAAGAAA others(3): Show |
intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0016 | a0001c0016t0016 | a0001c0016t0016g0311 | 1 | 37 | 0.0270 | 10 | c.174 others(29): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | TogoVar | |||||||
ARHGAP27_chr17_45388908_45437870 | 45411795 | T | TCACACAC others(3): Show |
intron_variant | MODIFIER | NA21309.hp2 | a0005 | a0005c0006 | a0005c0006t0015 | a0005c0006t0015g0191 | 1 | 289 | 0.0035 | 10 | c.658 others(27): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6729570 | G | GCACACAC others(3): Show |
upstream_gene_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0072 | 1 | 233 | 0.0043 | 10 | c.-25 others(19): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 145 | chr18 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6729574 | G | GCACACAC others(3): Show |
upstream_gene_variant | MODIFIER | HG01891.hp1 HG02080.hp1 HG02155.hp1 others(14): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0009a0001c0003t0003others(4): Show | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0121 others(14): Show |
17 | 176 | 0.0966 | 10 | c.-24 others(19): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 141 | chr18 | TogoVar |