| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| ARHGAP23_chr17_38423464_38517385 | 38504978 | CTTTTTTT others(11): Show |
C | intron_variant | MODIFIER | HG02055.hp1 HG03834.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0132a0001c0004t0001g0029 | 2 | 309 | 0.0065 | -18 | c.344 others(37): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
| ARHGAP24_chr4_85470150_86007666 | 85669644 | AATATATA others(11): Show |
A | intron_variant | MODIFIER | HG02486.hp1 NA21309.hp1 |
a0001 | a0001c0002a0001c0007 | a0001c0002t0002a0001c0007t0003 | a0001c0002t0002g0060a0001c0007t0003g0044 | 2 | 108 | 0.0185 | -18 | c.181 others(37): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
| ARHGAP24_chr4_85470150_86007666 | 85724489 | GTGTATAT others(11): Show |
G | intron_variant | MODIFIER | HG01069.hp1 HG01109.hp1 HG01109.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0007others(4): Show | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0001t0001g0067others(10): Show | 13 | 108 | 0.1204 | -18 | c.268 others(35): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
| ARHGAP24_chr4_85470150_86007666 | 85738367 | TTTATTAT others(11): Show |
T | intron_variant | MODIFIER | HG00323.hp1 HG01109.hp1 HG01168.hp2 others(14): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0013others(4): Show | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0026others(14): Show | 17 | 108 | 0.1574 | -18 | c.268 others(37): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
| ARHGAP24_chr4_85470150_86007666 | 85743392 | CAAAAAAA others(11): Show |
C | intron_variant | MODIFIER | HG02723.hp2 NA21309.hp2 |
a0001 | a0001c0003 | a0001c0003t0005a0001c0003t0010 | a0001c0003t0005g0059a0001c0003t0010g0083 | 2 | 108 | 0.0185 | -18 | c.268 others(37): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
| ARHGAP24_chr4_85470150_86007666 | 85997360 | TAGATGAT others(11): Show |
T | intron_variant | MODIFIER | HG01243.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
a0001 | a0001c0004 | a0001c0004t0003a0001c0004t0004 | a0001c0004t0003g0042a0001c0004t0003g0050a0001c0004t0003g0061others(4): Show | 7 | 108 | 0.0648 | -18 | c.200 others(37): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 9/9 | chr4 | TogoVar | ||||||
| ARHGAP25_chr2_68729811_68831833 | 68802898 | CACACATA others(11): Show |
C | intron_variant | MODIFIER | HG01255.hp1 HG02258.hp1 HG02735.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(1): Show | 4 | 368 | 0.0109 | -18 | c.467 others(35): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
| ARHGAP26_chr5_142765377_143234007 | 142808236 | GAAAAAAA others(11): Show |
G | intron_variant | MODIFIER | HG02970.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0104 | 1 | 198 | 0.0051 | -18 | c.154 others(37): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
| ARHGAP26_chr5_142765377_143234007 | 142890147 | AAAAAATA others(11): Show |
A | intron_variant | MODIFIER | HG03130.hp2 HG03453.hp1 HG03471.hp1 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0027a0001c0001t0053 | a0001c0001t0006g0096a0001c0001t0027g0097a0001c0001t0053g0082 | 3 | 198 | 0.0152 | -18 | c.487 others(35): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
| ARHGAP26_chr5_142765377_143234007 | 142890151 | AATATATA others(11): Show |
A | intron_variant | MODIFIER | HG02258.hp1 HG02647.hp1 HG02818.hp1 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0010a0001c0001t0026 | a0001c0001t0006g0086a0001c0001t0010g0080a0001c0001t0026g0071 | 3 | 198 | 0.0152 | -18 | c.487 others(35): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
| ARHGAP26_chr5_142765377_143234007 | 143167482 | CAAAAAAA others(11): Show |
C | intron_variant | MODIFIER | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(35): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0018a0001c0001t0001g0116a0001c0001t0001g0131others(35): Show | 38 | 198 | 0.1919 | -18 | c.198 others(39): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
| ARHGAP26_chr5_142765377_143234007 | 143194872 | CCTGCGCC others(11): Show |
C | intron_variant | MODIFIER | HG02257.hp2 HG02622.hp1 HG03471.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0029a0001c0001t0033a0001c0002t0004 | a0001c0001t0029g0085a0001c0001t0033g0053a0001c0002t0004g0100 | 3 | 198 | 0.0152 | -18 | c.198 others(39): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | chr5 | TogoVar | ||||||
| ARHGAP27_chr17_45388908_45437870 | 45419508 | GTATGTAT others(11): Show |
G | intron_variant | MODIFIER | HG02602.hp2 HG03130.hp1 |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0047a0002c0002t0001g0048 | 2 | 347 | 0.0058 | -18 | c.657 others(37): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | ||||||
| ARHGAP27_chr17_45388908_45437870 | 45419512 | GTATATAT others(11): Show |
G | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp2 HG00673.hp2 others(68): Show |
a0001a0006a0008 | a0001c0001a0006c0006a0008c0017 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0218a0001c0001t0001g0248a0001c0001t0001g0259others(56): Show | 71 | 347 | 0.2046 | -18 | c.657 others(37): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | ||||||
| ARHGAP28_chr18_6724716_6920716 | 6729554 | AGGAGCGC others(11): Show |
A | upstream_gene_variant | MODIFIER | HG02630.hp1 HG06807.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0022a0001c0003t0003 | a0001c0001t0022g0067a0001c0003t0003g0068 | 2 | 248 | 0.0081 | -18 | c.-26 others(27): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 161 | chr18 | TogoVar | ||||||
| ARHGAP28_chr18_6724716_6920716 | 6782592 | ATTTTTTT others(11): Show |
A | intron_variant | MODIFIER | HG02630.hp2 | a0008 | a0008c0011 | a0008c0011t0005 | a0008c0011t0005g0016 | 1 | 248 | 0.0040 | -18 | c.123 others(37): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
| ARHGAP28_chr18_6724716_6920716 | 6841190 | TCTCTCTC others(11): Show |
T | intron_variant | MODIFIER | HG01081.hp1 HG02071.hp2 NA19012.hp1 |
a0001a0002a0004 | a0001c0003a0002c0002a0004c0007 | a0001c0003t0003a0002c0002t0002a0004c0007t0002 | a0001c0003t0003g0222a0002c0002t0002g0196a0004c0007t0002g0036 | 3 | 248 | 0.0121 | -18 | c.543 others(35): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
| ARHGAP30_chr1_161041946_161074891 | 161051967 | TCACCACC others(11): Show |
T | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(61): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0014a0002c0002others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0014t0004others(5): Show | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0028others(60): Show | 64 | 390 | 0.1641 | -18 | c.101 others(35): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 9/11 | chr1 | TogoVar | ||||||
| ARHGAP30_chr1_161041946_161074891 | 161053462 | TTCTCTCT others(11): Show |
T | intron_variant | MODIFIER | HG02735.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0268 | 1 | 390 | 0.0026 | -18 | c.537 others(31): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 5/11 | chr1 | TogoVar | ||||||
| ARHGAP30_chr1_161041946_161074891 | 161064813 | AAGAAAGA others(11): Show |
A | intron_variant | MODIFIER | HG00642.hp2 HG01106.hp2 HG01175.hp2 others(26): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0001 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0014others(25): Show | 29 | 390 | 0.0744 | -18 | c.97+ others(33): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
| ARHGAP30_chr1_161041946_161074891 | 161072128 | CCAGCTCC others(11): Show |
C | upstream_gene_variant | MODIFIER | HG02004.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041 | 1 | 390 | 0.0026 | -18 | c.-25 others(29): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 2238 | chr1 | TogoVar | ||||||
| ARHGAP31_chr3_119289383_119425714 | 119297909 | AACACACA others(11): Show |
A | intron_variant | MODIFIER | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(3): Show |
a0001a0003a0004 | a0001c0005a0003c0006a0004c0007 | a0001c0005t0001a0003c0006t0001a0004c0007t0015 | a0001c0005t0001g0160a0001c0005t0001g0163a0001c0005t0001g0164others(3): Show | 6 | 310 | 0.0194 | -18 | c.100 others(35): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
| ARHGAP31_chr3_119289383_119425714 | 119332629 | TCTCTCTC others(11): Show |
T | intron_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0165 | 1 | 310 | 0.0032 | -18 | c.101 others(37): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
| ARHGAP31_chr3_119289383_119425714 | 119332631 | TCTCTCAC others(11): Show |
T | intron_variant | MODIFIER | HG02451.hp1 HG02602.hp1 HG02622.hp2 others(2): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0007a0001c0001t0020a0001c0002t0004others(2): Show | a0001c0001t0007g0241a0001c0001t0020g0010a0001c0002t0004g0291others(2): Show | 5 | 310 | 0.0161 | -18 | c.101 others(37): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
| ARHGAP32_chr11_128960060_129197325 | 128977851 | TTTATTAT others(11): Show |
T | intron_variant | MODIFIER | HG02523.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0048 | 1 | 398 | 0.0025 | -18 | c.212 others(35): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 19/22 | chr11 | TogoVar | ||||||
| ARHGAP32_chr11_128960060_129197325 | 129043889 | GGTGAAAA others(11): Show |
G | intron_variant | MODIFIER | NA18978.hp2 | a0001 | a0001c0002 | a0001c0002t0006 | a0001c0002t0006g0304 | 1 | 398 | 0.0025 | -18 | c.964 others(35): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 10/22 | chr11 | TogoVar | ||||||
| ARHGAP32_chr11_128960060_129197325 | 129063203 | ATATGCTA others(11): Show |
A | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp2 HG01258.hp2 others(29): Show |
a0001a0002a0007others(1): Show | a0001c0001a0001c0014a0002c0008others(3): Show | a0001c0001t0002a0001c0001t0004a0001c0014t0004others(4): Show | a0001c0001t0002g0156a0001c0001t0002g0158a0001c0001t0004g0154others(29): Show | 32 | 398 | 0.0804 | -18 | c.885 others(33): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 9/22 | chr11 | TogoVar | ||||||
| ARHGAP35_chr19_46855997_47010077 | 46888261 | AATATATA others(11): Show |
A | intron_variant | MODIFIER | HG01891.hp2 HG02015.hp1 HG02083.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0016others(1): Show | a0001c0001t0001g0169a0001c0001t0001g0278a0001c0001t0004g0022others(7): Show | 10 | 298 | 0.0336 | -18 | c.-18 others(39): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
| ARHGAP35_chr19_46855997_47010077 | 46898775 | AGCTGCTG others(11): Show |
A | intron_variant | MODIFIER | HG06807.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0284 | 1 | 298 | 0.0034 | -18 | c.-18 others(39): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
| ARHGAP42_chr11_100682288_100998941 | 100728713 | CGTATATA others(11): Show |
C | intron_variant | MODIFIER | HG01074.hp2 HG01175.hp1 HG01257.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002 | a0001c0001t0001g0178a0002c0002t0002g0018a0002c0002t0002g0019others(3): Show | 6 | 286 | 0.0210 | -18 | c.154 others(37): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar | ||||||
| ARHGAP42_chr11_100682288_100998941 | 100728714 | GTATATAT others(11): Show |
G | intron_variant | MODIFIER | NA18952.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0126 | 1 | 286 | 0.0035 | -18 | c.154 others(37): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
| ARHGAP42_chr11_100682288_100998941 | 100769712 | CTTTTTTT others(11): Show |
C | intron_variant | MODIFIER | NA19072.hp2 NA19075.hp2 NA19084.hp2 |
a0001a0006 | a0001c0001a0006c0017 | a0001c0001t0001a0001c0001t0002a0006c0017t0001 | a0001c0001t0001g0026a0001c0001t0002g0022a0006c0017t0001g0182 | 3 | 286 | 0.0105 | -18 | c.155 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
| ARHGAP42_chr11_100682288_100998941 | 100794075 | CAAAAAAA others(11): Show |
C | intron_variant | MODIFIER | HG00408.hp2 HG00544.hp2 HG00733.hp2 others(37): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0031others(8): Show | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0027others(37): Show | 40 | 286 | 0.1399 | -18 | c.251 others(34): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
| ARHGAP42_chr11_100682288_100998941 | 100875103 | CTCTCTGT others(11): Show |
C | intron_variant | MODIFIER | HG03453.hp1 NA18522.hp1 |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0008 | a0002c0002t0002g0174a0002c0002t0008g0175 | 2 | 286 | 0.0070 | -18 | c.384 others(37): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
| ARHGAP42_chr11_100682288_100998941 | 100903709 | AATATATA others(11): Show |
A | intron_variant | MODIFIER | HG01256.hp2 HG01978.hp2 HG02280.hp2 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002 | a0001c0001t0001g0084a0001c0001t0001g0088a0002c0002t0002g0102others(4): Show | 7 | 286 | 0.0245 | -18 | c.385 others(35): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
| ARHGAP42_chr11_100682288_100998941 | 100921202 | AATATATA others(11): Show |
A | intron_variant | MODIFIER | HG00738.hp1 HG02809.hp2 |
a0002 | a0002c0002a0002c0004 | a0002c0002t0002a0002c0004t0007 | a0002c0002t0002g0050a0002c0004t0007g0074 | 2 | 286 | 0.0070 | -18 | c.487 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
| ARHGAP42_chr11_100682288_100998941 | 100921231 | ATATATAT others(11): Show |
A | intron_variant | MODIFIER | HG00639.hp1 HG00741.hp1 HG02572.hp2 others(3): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0002c0004others(1): Show | a0001c0001t0002a0002c0002t0009a0002c0004t0007others(1): Show | a0001c0001t0002g0065a0002c0002t0009g0043a0002c0004t0007g0016others(3): Show | 6 | 286 | 0.0210 | -18 | c.487 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
| ARHGAP42_chr11_100682288_100998941 | 100921233 | ATATATAT others(11): Show |
A | intron_variant | MODIFIER | HG02630.hp2 HG02818.hp1 NA19240.hp2 others(1): Show |
a0002 | a0002c0002a0002c0006a0002c0009 | a0002c0002t0002a0002c0006t0008a0002c0006t0012others(1): Show | a0002c0002t0002g0045a0002c0006t0008g0240a0002c0006t0012g0176others(1): Show | 4 | 286 | 0.0140 | -18 | c.487 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
| ARHGAP44_chr17_12784498_12996643 | 12802927 | TTATATAT others(11): Show |
T | intron_variant | MODIFIER | HG01981.hp2 HG03017.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0006 | a0001c0001t0002g0023a0001c0001t0006g0024 | 2 | 230 | 0.0087 | -18 | c.53+ others(35): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
| ARHGAP44_chr17_12784498_12996643 | 12868589 | TTTTATAT others(11): Show |
T | intron_variant | MODIFIER | HG02809.hp2 HG02895.hp2 |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0005 | a0001c0001t0001g0212a0001c0005t0005g0087 | 2 | 230 | 0.0087 | -18 | c.54- others(35): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
| ARHGAP45_chr19_1062167_1091628 | 1066593 | TGGACGTG others(11): Show |
T | upstream_gene_variant | MODIFIER | HG02818.hp2 | a0018 | a0018c0055 | a0018c0055t0006 | a0018c0055t0006g0301 | 1 | 418 | 0.0024 | -18 | c.-81 others(27): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 573 | chr19 | TogoVar | ||||||
| ARHGAP5_chr14_32072304_32164728 | 32153406 | CAAAAAAA others(11): Show |
C | intron_variant | MODIFIER | NA19060.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014 | 1 | 186 | 0.0054 | -18 | c.418 others(35): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
| ARHGAP6_chrX_11132544_11670920 | 11176300 | CATATATA others(11): Show |
C | intron_variant | MODIFIER | HG02132.hp1 NA20752.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0011 | a0001c0001t0002g0128a0001c0001t0011g0001 | 2 | 144 | 0.0139 | -18 | c.162 others(37): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
| ARHGAP6_chrX_11132544_11670920 | 11354277 | CTCTCTCT others(11): Show |
C | intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0021 | 1 | 144 | 0.0069 | -18 | c.589 others(37): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
| ARHGAP6_chrX_11132544_11670920 | 11411183 | TTATATAT others(11): Show |
T | intron_variant | MODIFIER | HG01109.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0001a0001c0007t0001a0002c0002t0006others(1): Show | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0028others(3): Show | 6 | 144 | 0.0417 | -18 | c.589 others(39): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
| ARHGAP6_chrX_11132544_11670920 | 11473424 | GGTCACAT others(11): Show |
G | intron_variant | MODIFIER | HG03942.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0135 | 1 | 144 | 0.0069 | -18 | c.588 others(39): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
| ARHGAP6_chrX_11132544_11670920 | 11520131 | TTATATAT others(11): Show |
T | intron_variant | MODIFIER | NA19056.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0081 | 1 | 144 | 0.0069 | -18 | c.588 others(39): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
| ARHGAP6_chrX_11132544_11670920 | 11558836 | CAAAAAAA others(11): Show |
C | intron_variant | MODIFIER | NA18948.hp1 NA18966.hp1 NA18984.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0053a0001c0001t0001g0057a0001c0001t0001g0096others(2): Show | 5 | 144 | 0.0347 | -18 | c.588 others(39): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
| ARHGAP6_chrX_11132544_11670920 | 11590852 | AAAAGAAA others(11): Show |
A | intron_variant | MODIFIER | NA20805.hp1 | a0002 | a0002c0002 | a0002c0002t0009 | a0002c0002t0009g0140 | 1 | 144 | 0.0069 | -18 | c.588 others(37): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
| ARHGAP6_chrX_11132544_11670920 | 11660530 | CAAAAAAA others(11): Show |
C | intron_variant | MODIFIER | NA18948.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0053 | 1 | 144 | 0.0069 | -18 | c.588 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar |