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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP24_chr4_85470150_86007666 | 85997360 | TAGATGAT others(15): Show |
T | intron_variant | MODIFIER | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
a0001 | a0001c0005a0001c0007 | a0001c0005t0003a0001c0005t0004a0001c0005t0019others(2): Show | a0001c0005t0003g0085a0001c0005t0003g0094a0001c0005t0004g0034others(5): Show | 8 | 108 | 0.0741 | -22 | c.200 others(41): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 9/9 | chr4 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142808236 | GAAAAAAA others(15): Show |
G | intron_variant | MODIFIER | HG03041.hp1 HG03130.hp1 HG03453.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0006a0001c0001t0023others(1): Show | a0001c0001t0004g0098a0001c0001t0006g0095a0001c0001t0006g0096others(2): Show | 5 | 198 | 0.0253 | -22 | c.154 others(41): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142890149 | AAAATATA others(15): Show |
A | intron_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0101 | 1 | 198 | 0.0051 | -22 | c.487 others(39): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP27_chr17_45388908_45437870 | 45419512 | GTATATAT others(15): Show |
G | intron_variant | MODIFIER | HG01433.hp1 | a0004 | a0004c0004 | a0004c0004t0004 | a0004c0004t0004g0305 | 1 | 347 | 0.0029 | -22 | c.657 others(41): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6729327 | CACACACA others(15): Show |
C | upstream_gene_variant | MODIFIER | HG03486.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0168 | 1 | 248 | 0.0040 | -22 | c.-49 others(31): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 388 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6729552 | ACAGGAGC others(15): Show |
A | upstream_gene_variant | MODIFIER | HG01884.hp1 HG02896.hp1 HG02897.hp2 |
a0001a0004 | a0001c0001a0004c0007 | a0001c0001t0007a0004c0007t0004 | a0001c0001t0007g0116a0001c0001t0007g0117a0004c0007t0004g0115 | 3 | 248 | 0.0121 | -22 | c.-26 others(31): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 163 | chr18 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161064809 | AAGAAAGA others(15): Show |
A | intron_variant | MODIFIER | HG00544.hp2 HG00609.hp2 HG00673.hp1 others(34): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0003c0004t0001 | a0001c0001t0001g0009a0001c0001t0001g0012a0001c0001t0001g0015others(34): Show | 37 | 390 | 0.0949 | -22 | c.97+ others(37): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129193576 | ATATATTA others(15): Show |
A | upstream_gene_variant | MODIFIER | NA18947.hp1 NA18948.hp2 NA18951.hp2 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0006 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0017others(11): Show | 15 | 398 | 0.0377 | -22 | c.-14 others(33): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1252 | chr11 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46888261 | AATATATA others(15): Show |
A | intron_variant | MODIFIER | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(7): Show |
a0001a0004 | a0001c0001a0004c0008 | a0001c0001t0001a0001c0001t0004a0001c0001t0022others(2): Show | a0001c0001t0001g0195a0001c0001t0004g0072a0001c0001t0004g0235others(7): Show | 10 | 298 | 0.0336 | -22 | c.-18 others(43): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP36_chrX_131053346_131094885 | 131077764 | CATATATA others(15): Show |
C | intron_variant | MODIFIER | HG02486.hp1 HG02622.hp2 HG03540.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0154a0001c0001t0003g0039a0001c0001t0003g0153 | 3 | 302 | 0.0099 | -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 | 100699490 | ATATATAT others(15): Show |
A | intron_variant | MODIFIER | HG01884.hp1 | a0004 | a0004c0013 | a0004c0013t0038 | a0004c0013t0038g0236 | 1 | 286 | 0.0035 | -22 | c.154 others(41): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100699492 | ATATATAT others(15): Show |
A | intron_variant | MODIFIER | NA18522.hp2 | a0002 | a0002c0005 | a0002c0005t0010 | a0002c0005t0010g0056 | 1 | 286 | 0.0035 | -22 | c.154 others(41): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100728713 | CGTATATA others(15): Show |
C | intron_variant | MODIFIER | HG02895.hp2 HG02922.hp2 |
a0002 | a0002c0002 | a0002c0002t0011 | a0002c0002t0011g0207a0002c0002t0011g0231 | 2 | 286 | 0.0070 | -22 | c.154 others(41): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100728714 | GTATATAT others(15): Show |
G | intron_variant | MODIFIER | HG02056.hp1 | a0001 | a0001c0014 | a0001c0014t0001 | a0001c0014t0001g0132 | 1 | 286 | 0.0035 | -22 | c.154 others(41): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100779535 | TATACGTA others(15): Show |
T | intron_variant | MODIFIER | HG00738.hp2 HG01081.hp1 HG01891.hp1 others(4): Show |
a0002 | a0002c0002a0002c0005a0002c0009 | a0002c0002t0002a0002c0002t0008a0002c0002t0009others(2): Show | a0002c0002t0002g0139a0002c0002t0008g0028a0002c0002t0008g0029others(4): Show | 7 | 286 | 0.0245 | -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 | 100875101 | CTCTCTCT others(15): Show |
C | intron_variant | MODIFIER | HG01192.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0100 | 1 | 286 | 0.0035 | -22 | c.384 others(41): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | AATATATA others(15): Show |
A | intron_variant | MODIFIER | HG02896.hp1 | a0002 | a0002c0002 | a0002c0002t0008 | a0002c0002t0008g0009 | 1 | 286 | 0.0035 | -22 | c.385 others(39): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921202 | AATATATA others(15): Show |
A | intron_variant | MODIFIER | HG01175.hp2 HG01884.hp1 |
a0002a0004 | a0002c0002a0004c0013 | a0002c0002t0002a0004c0013t0038 | a0002c0002t0002g0085a0004c0013t0038g0236 | 2 | 286 | 0.0070 | -22 | c.487 others(37): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921227 | ATATATAT others(15): Show |
A | intron_variant | MODIFIER | HG01081.hp1 NA18906.hp2 |
a0002 | a0002c0002 | a0002c0002t0008 | a0002c0002t0008g0028a0002c0002t0008g0029 | 2 | 286 | 0.0070 | -22 | c.487 others(37): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921229 | ATATATAT others(15): Show |
A | intron_variant | MODIFIER | HG02055.hp1 HG02486.hp1 HG02818.hp2 others(1): Show |
a0001a0002 | a0001c0010a0002c0002 | a0001c0010t0001a0002c0002t0008a0002c0002t0039others(1): Show | a0001c0010t0001g0238a0002c0002t0008g0005a0002c0002t0039g0195others(1): Show | 4 | 286 | 0.0140 | -22 | c.487 others(37): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921231 | ATATATAT others(15): Show |
A | intron_variant | MODIFIER | HG00423.hp2 HG02896.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0019a0002c0002t0008 | a0001c0001t0019g0089a0002c0002t0008g0009 | 2 | 286 | 0.0070 | -22 | c.487 others(37): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921233 | ATATATAT others(15): Show |
A | intron_variant | MODIFIER | HG00544.hp2 HG02056.hp1 HG02071.hp1 others(4): Show |
a0001 | a0001c0001a0001c0014 | a0001c0001t0001a0001c0014t0001 | a0001c0001t0001g0023a0001c0001t0001g0070a0001c0001t0001g0091others(4): Show | 7 | 286 | 0.0245 | -22 | c.487 others(37): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921235 | ATATATAT others(15): Show |
A | intron_variant | MODIFIER | HG03139.hp2 | a0002 | a0002c0005 | a0002c0005t0016 | a0002c0005t0016g0032 | 1 | 286 | 0.0035 | -22 | c.487 others(37): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12802949 | ATATATAT others(15): Show |
A | intron_variant | MODIFIER | HG03831.hp1 | a0005 | a0005c0013 | a0005c0013t0003 | a0005c0013t0003g0055 | 1 | 230 | 0.0044 | -22 | c.53+ others(39): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12903136 | AGAGAGTG others(15): Show |
A | intron_variant | MODIFIER | HG02451.hp2 HG02622.hp1 HG02717.hp1 others(7): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0010a0001c0006t0001others(1): Show | a0001c0001t0001g0035a0001c0001t0001g0185a0001c0001t0001g0225others(7): Show | 10 | 230 | 0.0435 | -22 | c.199 others(39): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP6_chrX_11132544_11670920 | 11176300 | CATATATA others(15): Show |
C | intron_variant | MODIFIER | HG02622.hp1 HG06807.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0045a0001c0001t0002g0134 | 2 | 144 | 0.0139 | -22 | c.162 others(41): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11354273 | CTCTCTCT others(15): Show |
C | intron_variant | MODIFIER | NA20129.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0012 | 1 | 144 | 0.0069 | -22 | c.589 others(41): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11417059 | CATATATA others(15): Show |
C | intron_variant | MODIFIER | HG01255.hp1 HG02055.hp1 HG02809.hp1 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0003t0001 | a0001c0001t0001g0027a0001c0001t0002g0137a0001c0003t0001g0124others(1): Show | 4 | 144 | 0.0278 | -22 | c.589 others(43): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11503853 | CACACACA others(15): Show |
C | intron_variant | MODIFIER | HG01109.hp1 HG01258.hp1 HG01934.hp1 others(15): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0001a0001c0007t0001a0002c0002t0003others(1): Show | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0027others(15): Show | 18 | 144 | 0.1250 | -22 | c.588 others(43): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11520131 | TTATATAT others(15): Show |
T | intron_variant | MODIFIER | HG01167.hp1 NA20905.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0003 | a0001c0001t0002g0132a0002c0002t0003g0006 | 2 | 144 | 0.0139 | -22 | c.588 others(43): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590831 | GAAAAGAA others(15): Show |
G | intron_variant | MODIFIER | HG00609.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0108 | 1 | 144 | 0.0069 | -22 | c.588 others(41): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11660530 | CAAAAAAA others(15): Show |
C | intron_variant | MODIFIER | HG00280.hp1 HG01515.hp1 HG02698.hp1 others(6): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0015a0002c0002t0003others(1): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(6): Show | 9 | 144 | 0.0625 | -22 | c.588 others(39): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44852352 | ACCCTCTG others(15): Show |
A | intron_variant | MODIFIER | HG02809.hp2 HG02976.hp1 |
a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0173a0001c0001t0009g0321 | 2 | 390 | 0.0051 | -22 | c.877 others(39): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1831219 | GCCGTGGA others(15): Show |
G | intron_variant | MODIFIER | HG00597.hp2 HG01978.hp1 HG01981.hp2 others(11): Show |
a0001a0002a0007 | a0001c0006a0001c0011a0001c0069others(10): Show | a0001c0006t0001a0001c0011t0001a0001c0069t0001others(10): Show | a0001c0006t0001g0008a0001c0011t0001g0015a0001c0069t0001g0012others(11): Show | 14 | 363 | 0.0386 | -22 | c.-48 others(39): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1889159 | CGCTGAGT others(15): Show |
C | intron_variant | MODIFIER | HG00621.hp2 NA18994.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004 | a0001c0001t0002g0224a0001c0001t0004g0141 | 2 | 363 | 0.0055 | -22 | c.118 others(41): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1889164 | AGTTGGGG others(15): Show |
A | intron_variant | MODIFIER | HG02074.hp2 NA18942.hp1 NA18960.hp2 others(3): Show |
a0002 | a0002c0028a0002c0033a0002c0034others(3): Show | a0002c0028t0001a0002c0033t0002a0002c0034t0004others(3): Show | a0002c0028t0001g0223a0002c0033t0002g0006a0002c0034t0004g0148others(3): Show | 6 | 363 | 0.0165 | -22 | c.118 others(41): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 156994836 | AGGTAATA others(15): Show |
A | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(93): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0004others(2): Show | a0001c0001t0004a0001c0001t0006a0002c0002t0002others(10): Show | a0001c0001t0004g0130a0001c0001t0006g0088a0002c0002t0002g0001others(92): Show | 96 | 362 | 0.2652 | -22 | c.33- others(37): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF16_chr1_3449665_3486113 | 3474453 | TGGCCGAG others(15): Show |
T | intron_variant | MODIFIER | HG01099.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0181 | 1 | 334 | 0.0030 | -22 | c.130 others(39): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF16_chr1_3449665_3486113 | 3485931 | CAAAAAAA others(15): Show |
C | downstream_gene_variant | MODIFIER | HG01243.hp2 HG02809.hp1 HG02896.hp2 others(7): Show |
a0002a0003 | a0002c0017a0002c0035a0003c0006 | a0002c0017t0001a0002c0035t0002a0003c0006t0002others(1): Show | a0002c0017t0001g0283a0002c0017t0001g0284a0002c0035t0002g0301others(4): Show | 10 | 334 | 0.0299 | -22 | c.*53 others(33): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4819 | chr1 | TogoVar | ||||||
ARHGEF17_chr11_73303276_73374388 | 73329322 | CATATATA others(15): Show |
C | intron_variant | MODIFIER | HG01106.hp2 HG01884.hp2 HG06807.hp2 |
a0002 | a0002c0008a0002c0035 | a0002c0008t0002a0002c0008t0006a0002c0035t0006 | a0002c0008t0002g0139a0002c0008t0006g0142a0002c0035t0006g0141 | 3 | 228 | 0.0132 | -22 | c.319 others(43): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF17_chr11_73303276_73374388 | 73329355 | ATATATAT others(15): Show |
A | intron_variant | MODIFIER | HG01891.hp2 HG02809.hp2 |
a0001 | a0001c0001a0001c0029 | a0001c0001t0001a0001c0029t0001 | a0001c0001t0001g0080a0001c0029t0001g0079 | 2 | 228 | 0.0088 | -22 | c.319 others(43): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7350763 | GGTGGGTG others(15): Show |
G | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG00609.hp2 others(23): Show |
a0001a0002a0003others(5): Show | a0001c0001a0002c0004a0002c0005others(7): Show | a0001c0001t0002a0001c0001t0011a0002c0004t0002others(10): Show | a0001c0001t0002g0237a0001c0001t0011g0223a0001c0001t0011g0224others(23): Show | 26 | 298 | 0.0873 | -22 | c.-11 others(41): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7355068 | TCACACAC others(15): Show |
T | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(48): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0048a0002c0004others(17): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(25): Show | a0001c0001t0002g0237a0001c0001t0004g0293a0001c0001t0005g0291others(48): Show | 51 | 298 | 0.1711 | -22 | c.-11 others(41): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154239289 | AGAGAGAG others(15): Show |
A | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(40): Show |
a0001a0002a0008others(1): Show | a0001c0001a0001c0015a0002c0002others(4): Show | a0001c0001t0002a0001c0001t0009a0001c0001t0011others(8): Show | a0001c0001t0002g0002a0001c0001t0002g0142a0001c0001t0002g0152others(39): Show | 43 | 283 | 0.1519 | -22 | c.209 others(41): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF26_chr3_154116390_154262825 | 154239291 | AGAGAGAG others(15): Show |
A | intron_variant | MODIFIER | NA18948.hp2 NA18969.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0271a0001c0001t0002g0272 | 2 | 283 | 0.0071 | -22 | c.209 others(41): Show |
ARHGEF26 | ENSG00000114790.13 | transcript | ENST00000465093.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73671694 | TTATATAT others(15): Show |
T | intron_variant | MODIFIER | HG01261.hp2 HG01891.hp2 |
a0002a0004 | a0002c0029a0004c0018 | a0002c0029t0001a0004c0018t0002 | a0002c0029t0001g0091a0004c0018t0002g0154 | 2 | 188 | 0.0106 | -22 | c.-11 others(41): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73741365 | GTGTGTGT others(15): Show |
G | intron_variant | MODIFIER | HG00438.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0008 | 1 | 188 | 0.0053 | -22 | c.34- others(37): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73741379 | GTGTGTGT others(15): Show |
G | intron_variant | MODIFIER | NA18906.hp1 NA19007.hp2 |
a0005a0018 | a0005c0022a0018c0026 | a0005c0022t0005a0018c0026t0001 | a0005c0022t0005g0119a0018c0026t0001g0060 | 2 | 188 | 0.0106 | -22 | c.34- others(37): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73741381 | GTGTGTAT others(15): Show |
G | intron_variant | MODIFIER | HG02145.hp1 NA18961.hp1 |
a0018a0036 | a0018c0026a0036c0055 | a0018c0026t0002a0036c0055t0001 | a0018c0026t0002g0030a0036c0055t0001g0135 | 2 | 188 | 0.0106 | -22 | c.34- others(37): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73741383 | GTGTATAT others(15): Show |
G | intron_variant | MODIFIER | HG03492.hp2 | a0002 | a0002c0032 | a0002c0032t0002 | a0002c0032t0002g0065 | 1 | 188 | 0.0053 | -22 | c.34- others(37): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |