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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(6): Show |
intron_variant | MODIFIER | NA19002.hp2 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0223 | 1 | 352 | 0.0028 | 13 | c.495 others(30): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(6): Show |
intron_variant | MODIFIER | HG02080.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0312 | 1 | 352 | 0.0028 | 13 | c.495 others(30): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(6): Show |
intron_variant | MODIFIER | HG00642.hp1 NA18994.hp2 NA18998.hp2 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0001a0001c0001t0002a0003c0003t0001 | a0001c0001t0001g0252a0001c0001t0002g0311a0003c0003t0001g0175 | 3 | 352 | 0.0085 | 13 | c.495 others(30): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(6): Show |
intron_variant | MODIFIER | HG01069.hp2 NA19055.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0217a0001c0001t0001g0271 | 2 | 352 | 0.0057 | 13 | c.495 others(30): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628983 | T | TATATATA others(6): Show |
intron_variant | MODIFIER | HG02280.hp1 HG03927.hp2 NA18994.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0005a0002c0002t0001 | a0001c0001t0001g0141a0001c0001t0005g0001a0002c0002t0001g0051 | 3 | 352 | 0.0085 | 13 | c.495 others(30): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38447437 | G | GAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG00621.hp2 HG00733.hp2 HG01099.hp1 others(11): Show |
a0001a0010a0014others(1): Show | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0012others(5): Show | a0001c0001t0001g0056a0001c0001t0001g0078a0001c0001t0001g0098others(11): Show | 14 | 309 | 0.0453 | 13 | c.64- others(30): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP23_chr17_38423464_38517385 | 38447453 | A | AAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG02135.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0119 | 1 | 309 | 0.0032 | 13 | c.64- others(30): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP23_chr17_38423464_38517385 | 38494492 | G | GGTGGGAG others(6): Show |
intron_variant | MODIFIER | NA18963.hp1 | a0008 | a0008c0049 | a0008c0049t0001 | a0008c0049t0001g0266 | 1 | 309 | 0.0032 | 13 | c.327 others(32): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 20/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85485376 | A | AAAAAAAT others(6): Show |
intron_variant | MODIFIER | HG03471.hp1 | a0001 | a0001c0002 | a0001c0002t0008 | a0001c0002t0008g0052 | 1 | 108 | 0.0093 | 13 | c.-21 others(30): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85640905 | T | TTTGGCAC others(6): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00735.hp2 others(33): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(8): Show | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0018others(33): Show | 36 | 108 | 0.3333 | 13 | c.180 others(32): 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(6): Show |
intron_variant | MODIFIER | HG02451.hp2 HG02615.hp1 HG02717.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0005a0001c0002t0016others(1): Show | a0001c0001t0001g0067a0001c0001t0005g0075a0001c0002t0016g0055others(1): Show | 4 | 108 | 0.0370 | 13 | c.181 others(32): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85731161 | A | AACTACCA others(6): Show |
intron_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0049 | 1 | 108 | 0.0093 | 13 | c.268 others(30): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85731164 | C | CACCACAT others(6): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0020others(26): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(93): Show | 96 | 108 | 0.8889 | 13 | c.268 others(30): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85733060 | C | CTTTTTTT others(6): Show |
intron_variant | MODIFIER | HG00639.hp2 HG02258.hp2 HG02622.hp2 others(4): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0015a0001c0002t0007others(3): Show | a0001c0001t0001g0043a0001c0001t0001g0062a0001c0001t0015g0049others(4): Show | 7 | 108 | 0.0648 | 13 | c.268 others(32): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142890136 | T | TAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG00609.hp1 HG02132.hp2 NA18954.hp2 others(3): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0138a0001c0001t0002g0135a0001c0001t0003g0015others(3): Show | 6 | 198 | 0.0303 | 13 | c.487 others(30): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142890151 | A | AAAAAAAT others(6): Show |
intron_variant | MODIFIER | NA19068.hp2 | a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0178 | 1 | 198 | 0.0051 | 13 | c.487 others(30): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142890151 | A | AAAAATAT others(6): Show |
intron_variant | MODIFIER | HG02280.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0087 | 1 | 198 | 0.0051 | 13 | c.487 others(30): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142936146 | C | CACACACA others(6): Show |
intron_variant | MODIFIER | HG03471.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0096 | 1 | 198 | 0.0051 | 13 | c.110 others(32): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949204 | A | AGAGAGAG others(6): Show |
intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0001 | a0001c0001t0023 | a0001c0001t0023g0055 | 1 | 198 | 0.0051 | 13 | c.110 others(34): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949221 | G | GAGAGAGA others(6): Show |
intron_variant | MODIFIER | HG02056.hp1 NA19240.hp1 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0041 | a0001c0001t0004g0056a0001c0001t0041g0163 | 2 | 198 | 0.0101 | 13 | c.110 others(34): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142955125 | C | CACACACA others(6): Show |
intron_variant | MODIFIER | NA19090.hp1 NA19090.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0002 | a0001c0001t0001g0153a0001c0003t0002g0125 | 2 | 198 | 0.0101 | 13 | c.110 others(34): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143012576 | T | TATATATA others(6): Show |
intron_variant | MODIFIER | NA18612.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0184 | 1 | 198 | 0.0051 | 13 | c.110 others(32): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143087636 | C | CTTTTTTT others(6): Show |
intron_variant | MODIFIER | HG00558.hp1 HG00597.hp2 HG02155.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0158a0001c0001t0002g0005a0001c0001t0002g0006others(10): Show | 13 | 198 | 0.0657 | 13 | c.153 others(34): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143092862 | T | TTAGGCAA others(6): Show |
intron_variant | MODIFIER | HG01934.hp1 HG02723.hp1 |
a0001 | a0001c0001 | a0001c0001t0015a0001c0001t0042 | a0001c0001t0015g0037a0001c0001t0042g0042 | 2 | 198 | 0.0101 | 13 | c.153 others(34): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143167482 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG01243.hp1 | a0001 | a0001c0001 | a0001c0001t0021 | a0001c0001t0021g0079 | 1 | 198 | 0.0051 | 13 | c.198 others(34): 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(6): Show |
intron_variant | MODIFIER | HG02056.hp2 NA18956.hp1 NA19068.hp2 |
a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0002a0001c0003t0002a0001c0004t0007 | a0001c0001t0002g0005a0001c0003t0002g0178a0001c0004t0007g0054 | 3 | 198 | 0.0152 | 13 | c.198 others(34): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143232630 | C | CTTTTTTT others(6): Show |
downstream_gene_variant | MODIFIER | HG02257.hp2 HG02965.hp1 HG03130.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0023others(6): Show | a0001c0001t0002g0023a0001c0001t0002g0190a0001c0001t0004g0105others(7): Show | 10 | 198 | 0.0505 | 13 | c.*10 others(26): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 3624 | chr5 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6841180 | C | CTCTCTCT others(6): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0228 | 1 | 248 | 0.0040 | 13 | c.543 others(30): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6841203 | C | CTCTCTCT others(6): Show |
intron_variant | MODIFIER | HG01952.hp1 | a0003 | a0003c0004 | a0003c0004t0001 | a0003c0004t0001g0024 | 1 | 248 | 0.0040 | 13 | c.543 others(30): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6841212 | T | TCTCTCTC others(6): Show |
intron_variant | MODIFIER | HG00558.hp2 HG00621.hp1 |
a0003 | a0003c0004 | a0003c0004t0001 | a0003c0004t0001g0032a0003c0004t0001g0048 | 2 | 248 | 0.0081 | 13 | c.543 others(30): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP30_chr1_161041946_161074891 | 161055876 | A | AAATAAAA others(6): Show |
intron_variant | MODIFIER | NA18983.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0013 | 1 | 390 | 0.0026 | 13 | c.345 others(28): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128991380 | T | TACATTTA others(6): Show |
intron_variant | MODIFIER | NA18943.hp2 NA18971.hp2 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0173a0001c0001t0004g0175 | 2 | 398 | 0.0050 | 13 | c.119 others(32): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 12/22 | chr11 | TogoVar | ||||||
ARHGAP33_chr19_35770564_35793822 | 35771989 | C | CTTTTTTT others(6): Show |
upstream_gene_variant | MODIFIER | HG02486.hp2 HG02976.hp1 HG03540.hp1 others(5): Show |
a0001a0011a0015 | a0001c0002a0001c0006a0011c0027others(1): Show | a0001c0002t0001a0001c0006t0001a0011c0027t0001others(1): Show | a0001c0002t0001g0001a0001c0002t0001g0018a0001c0006t0001g0019others(3): Show | 8 | 420 | 0.0191 | 13 | c.-36 others(24): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3574 | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46983054 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG02015.hp2 | a0002 | a0002c0004 | a0002c0004t0003 | a0002c0004t0003g0003 | 1 | 298 | 0.0034 | 13 | c.382 others(32): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100837666 | C | CTTTTTTT others(6): Show |
intron_variant | MODIFIER | HG01257.hp2 HG01884.hp2 HG02071.hp2 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0002others(2): Show | a0001c0001t0001g0086a0001c0001t0001g0117a0001c0001t0001g0145others(4): Show | 7 | 286 | 0.0245 | 13 | c.313 others(32): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100858086 | G | GTGTGTGT others(6): Show |
intron_variant | MODIFIER | HG02602.hp1 NA18943.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0113a0001c0001t0001g0188 | 2 | 286 | 0.0070 | 13 | c.313 others(30): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903706 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG01081.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0073 | 1 | 286 | 0.0035 | 13 | c.385 others(30): 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(6): Show |
intron_variant | MODIFIER | HG01175.hp1 HG01175.hp2 HG02145.hp2 others(3): Show |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0008a0002c0002t0021 | a0002c0002t0002g0019a0002c0002t0002g0050a0002c0002t0002g0085others(3): Show | 6 | 286 | 0.0210 | 13 | c.245 others(32): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTTTTTT others(6): Show |
intron_variant | MODIFIER | HG02132.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0203 | 1 | 286 | 0.0035 | 13 | c.245 others(32): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP45_chr19_1062167_1091628 | 1069535 | G | GGCCAGGG others(6): Show |
intron_variant | MODIFIER | HG02647.hp1 NA19240.hp2 |
a0004 | a0004c0028 | a0004c0028t0002 | a0004c0028t0002g0038 | 2 | 418 | 0.0048 | 13 | c.421 others(28): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 2/22 | chr19 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1072014 | T | TTTCTTTT others(6): Show |
intron_variant | MODIFIER | HG02257.hp2 | a0003 | a0003c0040 | a0003c0040t0028 | a0003c0040t0028g0144 | 1 | 418 | 0.0024 | 13 | c.422 others(30): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP5_chr14_32072304_32164728 | 32156288 | T | TATTTGGT others(6): Show |
3_prime_UTR_variant | MODIFIER | NA19088.hp1 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0171 | 1 | 186 | 0.0054 | 13 | c.*13 others(24): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 7/7 | 1352 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||
ARHGAP6_chrX_11132544_11670920 | 11202799 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | NA19240.hp1 | a0002 | a0002c0005 | a0002c0005t0006 | a0002c0005t0006g0018 | 1 | 144 | 0.0069 | 13 | c.749 others(30): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11497559 | T | TCTCTCTC others(6): Show |
intron_variant | MODIFIER | NA19082.hp1 | a0002 | a0002c0002 | a0002c0002t0016 | a0002c0002t0016g0007 | 1 | 144 | 0.0069 | 13 | c.588 others(34): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590921 | A | AAAGAAAA others(6): Show |
intron_variant | MODIFIER | HG02055.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0125 | 1 | 144 | 0.0069 | 13 | c.588 others(32): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44767984 | C | CTTTTTTT others(6): Show |
intron_variant | MODIFIER | NA18948.hp2 | a0002 | a0002c0003 | a0002c0003t0004 | a0002c0003t0004g0245 | 1 | 390 | 0.0026 | 13 | c.-72 others(32): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44818450 | C | CAAAAAAA others(6): Show |
intron_variant | MODIFIER | HG01243.hp1 HG01516.hp2 HG01517.hp2 others(22): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0007a0001c0009others(12): Show | a0001c0001t0001a0001c0001t0003a0001c0007t0001others(13): Show | a0001c0001t0001g0097a0001c0001t0001g0370a0001c0001t0003g0074others(22): Show | 25 | 390 | 0.0641 | 13 | c.386 others(30): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44827336 | G | GTTTTTTT others(6): Show |
intron_variant | MODIFIER | HG01109.hp2 HG03704.hp2 |
a0002 | a0002c0003a0002c0064 | a0002c0003t0004a0002c0064t0005 | a0002c0003t0004g0177a0002c0064t0005g0067 | 2 | 390 | 0.0051 | 13 | c.596 others(30): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44833096 | C | CTTTTCTT others(6): Show |
intron_variant | MODIFIER | NA20129.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0198 | 1 | 390 | 0.0026 | 13 | c.596 others(30): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44867283 | C | CAAAAAAA others(6): Show |
downstream_gene_variant | MODIFIER | HG00735.hp2 HG02132.hp1 HG02698.hp2 others(1): Show |
a0001 | a0001c0001a0001c0004a0001c0010 | a0001c0001t0001a0001c0004t0001a0001c0010t0001 | a0001c0001t0001g0200a0001c0004t0001g0181a0001c0010t0001g0243others(1): Show | 4 | 390 | 0.0103 | 13 | c.*46 others(24): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 4500 | chr22 | TogoVar |