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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP15_chr2_143124419_143773352 | 143320404 | C | CCCCCCCC others(15): Show |
intron_variant | MODIFIER | HG02074.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0025 | 1 | 162 | 0.0062 | 22 | c.474 others(41): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGCGCGCG others(15): Show |
intron_variant | MODIFIER | HG02145.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041 | 1 | 162 | 0.0062 | 22 | c.475 others(41): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGTGCG others(15): Show |
intron_variant | MODIFIER | HG02148.hp1 HG02148.hp2 HG03654.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0056a0001c0001t0001g0070a0001c0001t0001g0073others(3): Show | 6 | 162 | 0.0370 | 22 | c.475 others(41): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGTGTG others(15): Show |
intron_variant | MODIFIER | NA18991.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0086 | 1 | 162 | 0.0062 | 22 | c.475 others(41): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGTGTG others(15): Show |
intron_variant | MODIFIER | HG02129.hp2 NA18970.hp2 NA18986.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0071a0001c0001t0001g0084a0001c0001t0001g0158others(1): Show | 4 | 162 | 0.0247 | 22 | c.475 others(41): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGTGTG others(15): Show |
intron_variant | MODIFIER | HG03225.hp2 HG03486.hp1 NA18947.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0082a0001c0001t0001g0092a0001c0001t0001g0097 | 3 | 162 | 0.0185 | 22 | c.475 others(41): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGTGTG others(15): Show |
intron_variant | MODIFIER | HG00642.hp2 HG01358.hp2 HG02572.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0027a0001c0001t0001g0032a0001c0001t0001g0098others(5): Show | 8 | 162 | 0.0494 | 22 | c.475 others(41): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143606035 | C | CAAAAAAA others(15): Show |
intron_variant | MODIFIER | NA19068.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0160 | 1 | 162 | 0.0062 | 22 | c.100 others(43): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143656934 | G | GGTGTGTG others(15): Show |
intron_variant | MODIFIER | HG01071.hp2 HG03491.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0021a0001c0001t0001g0067 | 2 | 162 | 0.0124 | 22 | c.113 others(43): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673746 | G | GTATATAT others(15): Show |
intron_variant | MODIFIER | HG00609.hp2 HG00741.hp2 NA18975.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0077a0001c0001t0001g0146a0001c0001t0001g0149others(1): Show | 4 | 162 | 0.0247 | 22 | c.113 others(43): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673748 | G | GTATATAT others(15): Show |
intron_variant | MODIFIER | HG01515.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0043 | 1 | 162 | 0.0062 | 22 | c.113 others(43): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673756 | G | GTATATAT others(15): Show |
intron_variant | MODIFIER | NA18953.hp2 NA18966.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0052a0001c0001t0001g0087 | 2 | 162 | 0.0124 | 22 | c.113 others(43): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | G | GTATATAT others(15): Show |
intron_variant | MODIFIER | HG02129.hp2 HG03942.hp1 HG04199.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0049a0001c0001t0001g0069a0001c0001t0001g0084others(2): Show | 5 | 162 | 0.0309 | 22 | c.113 others(43): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | G | GTGTATAT others(15): Show |
intron_variant | MODIFIER | NA18947.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0082 | 1 | 162 | 0.0062 | 22 | c.113 others(43): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | G | GTGTGTAT others(15): Show |
intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 | 1 | 162 | 0.0062 | 22 | c.113 others(43): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673781 | T | TATATATA others(15): Show |
intron_variant | MODIFIER | HG02300.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0064 | 1 | 162 | 0.0062 | 22 | c.113 others(43): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP17_chr16_24914389_25020369 | 24950836 | C | CAAAAAAA others(15): Show |
intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014 | 1 | 240 | 0.0042 | 22 | c.104 others(41): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110687035 | C | CATATATA others(15): Show |
intron_variant | MODIFIER | HG02922.hp1 HG03139.hp2 HG03209.hp1 others(6): Show |
a0001a0002a0006others(1): Show | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0170a0001c0001t0001g0191a0001c0001t0002g0206others(6): Show | 9 | 226 | 0.0398 | 22 | c.188 others(39): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(15): Show |
intron_variant | MODIFIER | HG00323.hp2 HG02895.hp2 |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0110a0002c0002t0001g0131 | 2 | 352 | 0.0057 | 22 | c.495 others(39): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(15): Show |
intron_variant | MODIFIER | HG02145.hp1 | a0004 | a0004c0004 | a0004c0004t0001 | a0004c0004t0001g0089 | 1 | 352 | 0.0028 | 22 | c.495 others(39): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38513074 | T | TTAAATAT others(15): Show |
downstream_gene_variant | MODIFIER | HG01071.hp2 HG01106.hp1 HG02630.hp1 others(3): Show |
a0001 | a0001c0001a0001c0004a0001c0016 | a0001c0001t0001a0001c0001t0014a0001c0004t0001others(1): Show | a0001c0001t0001g0064a0001c0001t0001g0222a0001c0001t0001g0305others(3): Show | 6 | 309 | 0.0194 | 22 | c.*21 others(33): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 690 | chr17 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85655792 | T | TATATATA others(15): Show |
intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0090 | 1 | 108 | 0.0093 | 22 | c.181 others(41): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85655804 | G | GAGAGAGA others(15): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0104 | 1 | 108 | 0.0093 | 22 | c.181 others(41): 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(15): Show |
intron_variant | MODIFIER | HG02145.hp2 HG02486.hp2 HG03130.hp2 |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0005a0002c0006t0018 | a0001c0001t0005g0036a0001c0001t0005g0101a0002c0006t0018g0040 | 3 | 108 | 0.0278 | 22 | c.268 others(41): 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(15): Show |
intron_variant | MODIFIER | HG02622.hp1 | a0001 | a0001c0008 | a0001c0008t0014 | a0001c0008t0014g0063 | 1 | 108 | 0.0093 | 22 | c.268 others(41): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949190 | A | AGAGAGAG others(15): Show |
intron_variant | MODIFIER | HG02615.hp1 HG04228.hp2 |
a0001a0002 | a0001c0001a0002c0007 | a0001c0001t0003a0002c0007t0004 | a0001c0001t0003g0191a0002c0007t0004g0110 | 2 | 198 | 0.0101 | 22 | c.110 others(43): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949232 | G | GAGAGAGA others(15): Show |
intron_variant | MODIFIER | HG01192.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0108 | 1 | 198 | 0.0051 | 22 | c.110 others(43): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949232 | G | GAGAGAGA others(15): Show |
intron_variant | MODIFIER | HG01175.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0109 | 1 | 198 | 0.0051 | 22 | c.110 others(43): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142963194 | A | ATACATAT others(15): Show |
intron_variant | MODIFIER | HG02451.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0046 | 1 | 198 | 0.0051 | 22 | c.110 others(43): 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(15): Show |
intron_variant | MODIFIER | NA18944.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0137 | 1 | 198 | 0.0051 | 22 | c.110 others(43): 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(15): Show |
intron_variant | MODIFIER | HG03195.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0022 | 1 | 198 | 0.0051 | 22 | c.110 others(43): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143012537 | T | TTATATAT others(15): Show |
intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0002 | 1 | 198 | 0.0051 | 22 | c.110 others(41): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143012552 | C | CATATATA others(15): Show |
intron_variant | MODIFIER | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(5): Show |
a0001 | a0001c0001a0001c0003a0001c0006 | a0001c0001t0011a0001c0001t0014a0001c0001t0019others(4): Show | a0001c0001t0011g0091a0001c0001t0014g0038a0001c0001t0019g0010others(5): Show | 8 | 198 | 0.0404 | 22 | c.110 others(41): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143012576 | T | TATATATA others(15): Show |
intron_variant | MODIFIER | NA18950.hp2 NA18978.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0001 | a0001c0001t0002g0013a0001c0002t0001g0130 | 2 | 198 | 0.0101 | 22 | c.110 others(41): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143167482 | C | CAAAAAAA others(15): Show |
intron_variant | MODIFIER | HG02818.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0086 | 1 | 198 | 0.0051 | 22 | c.198 others(43): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6729574 | G | GCACACAC others(15): Show |
upstream_gene_variant | MODIFIER | HG01346.hp1 HG02615.hp1 HG03041.hp1 others(2): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0023others(2): Show | a0001c0001t0001a0002c0002t0002a0003c0023t0001others(2): Show | a0001c0001t0001g0150a0002c0002t0002g0148a0003c0023t0001g0120others(2): Show | 5 | 248 | 0.0202 | 22 | c.-24 others(31): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 141 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6729574 | G | GCGCACAC others(15): Show |
upstream_gene_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0018 | a0001c0018t0020 | a0001c0018t0020g0007 | 1 | 248 | 0.0040 | 22 | c.-24 others(31): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 141 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATATAT others(15): Show |
intron_variant | MODIFIER | HG02523.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0010others(1): Show | a0001c0001t0001a0001c0003t0003a0001c0010t0003others(1): Show | a0001c0001t0001g0097a0001c0003t0003g0094a0001c0003t0003g0095others(2): Show | 5 | 248 | 0.0202 | 22 | c.122 others(37): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6730236 | T | TATATATA others(15): Show |
intron_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0085 | 1 | 248 | 0.0040 | 22 | c.122 others(37): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119293703 | A | AGTGTGTG others(15): Show |
upstream_gene_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(12): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0005a0001c0001t0006a0001c0002t0001others(4): Show | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(12): Show | 15 | 310 | 0.0484 | 22 | c.-12 others(33): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 679 | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119297909 | A | AACACACA others(15): Show |
intron_variant | MODIFIER | HG03130.hp2 HG03471.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0020a0001c0004t0021 | a0001c0001t0020g0056a0001c0004t0021g0055 | 2 | 310 | 0.0065 | 22 | c.100 others(39): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119307940 | C | CAAAAAAA others(15): Show |
intron_variant | MODIFIER | HG01243.hp1 HG02293.hp2 NA18945.hp2 others(8): Show |
a0001a0005a0011 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0005a0001c0001t0006a0001c0002t0001others(3): Show | a0001c0001t0005g0111a0001c0001t0006g0102a0001c0001t0006g0103others(8): Show | 11 | 310 | 0.0355 | 22 | c.100 others(41): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119388306 | T | TTACATAT others(15): Show |
intron_variant | MODIFIER | HG00597.hp1 HG01081.hp1 HG01192.hp2 others(8): Show |
a0001a0004a0013 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0008a0001c0001t0018a0001c0001t0020others(8): Show | a0001c0001t0008g0200a0001c0001t0018g0209a0001c0001t0020g0043others(8): Show | 11 | 310 | 0.0355 | 22 | c.683 others(39): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP32_chr11_128960060_129197325 | 129143072 | C | CATATATA others(15): Show |
intron_variant | MODIFIER | HG00423.hp1 HG00609.hp1 HG00673.hp2 others(26): Show |
a0001a0002 | a0001c0001a0001c0016a0002c0004 | a0001c0001t0002a0001c0001t0004a0001c0001t0038others(3): Show | a0001c0001t0002g0002a0001c0001t0002g0111a0001c0001t0002g0112others(25): Show | 29 | 398 | 0.0729 | 22 | c.226 others(41): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131077764 | C | CATATATA others(15): Show |
intron_variant | MODIFIER | NA19000.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0068 | 1 | 302 | 0.0033 | 22 | c.-14 others(41): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100779567 | T | TATACGTA others(15): Show |
intron_variant | MODIFIER | NA19070.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0081 | 1 | 286 | 0.0035 | 22 | c.250 others(39): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100837666 | C | CTTTTTTT others(15): Show |
intron_variant | MODIFIER | NA18970.hp2 NA19054.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0141a0001c0001t0001g0200 | 2 | 286 | 0.0070 | 22 | c.313 others(41): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100858117 | G | GTGTGTGT others(15): Show |
intron_variant | MODIFIER | HG01243.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0249 | 1 | 286 | 0.0035 | 22 | c.313 others(39): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCGCACAC others(15): Show |
intron_variant | MODIFIER | HG02132.hp1 NA19068.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0117a0001c0001t0001g0134 | 2 | 286 | 0.0070 | 22 | c.385 others(41): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCTTTT others(15): Show |
intron_variant | MODIFIER | HG00735.hp2 HG03834.hp2 |
a0002a0005 | a0002c0002a0005c0016 | a0002c0002t0012a0005c0016t0012 | a0002c0002t0012g0024a0005c0016t0012g0103 | 2 | 286 | 0.0070 | 22 | c.245 others(41): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |