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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP33_chr19_35770564_35793822 | 35773965 | CTTTTTTT others(5): Show |
C | upstream_gene_variant | MODIFIER | HG01256.hp2 HG01258.hp2 HG02080.hp2 others(6): Show |
a0001a0010 | a0001c0001a0001c0005a0010c0028 | a0001c0001t0001a0001c0005t0001a0010c0028t0001 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(5): Show | 9 | 420 | 0.0214 | -12 | c.-16 others(23): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1598 | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46869476 | TTGTGTGT others(5): Show |
T | intron_variant | MODIFIER | HG02257.hp2 | a0001 | a0001c0001 | a0001c0001t0030 | a0001c0001t0030g0277 | 1 | 298 | 0.0034 | -12 | c.-18 others(31): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46888261 | AATATATA others(5): Show |
A | intron_variant | MODIFIER | HG00280.hp1 HG00733.hp1 HG01169.hp2 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0130a0001c0001t0001g0142a0001c0001t0001g0202others(10): Show | 13 | 298 | 0.0436 | -12 | c.-18 others(33): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46939372 | CATTTATT others(5): Show |
C | intron_variant | MODIFIER | HG02559.hp1 HG02630.hp2 HG03139.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0069a0001c0001t0014g0087a0001c0001t0014g0247others(1): Show | 4 | 298 | 0.0134 | -12 | c.382 others(31): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46983054 | CAAAAAAA others(5): Show |
C | intron_variant | MODIFIER | HG03041.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0014 | 1 | 298 | 0.0034 | -12 | c.382 others(31): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 47006267 | CTTTTTTT others(5): Show |
C | downstream_gene_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG02622.hp1 others(3): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0001t0024a0001c0001t0038others(1): Show | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0024g0032others(3): Show | 6 | 298 | 0.0201 | -12 | c.*55 others(23): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1191 | chr19 | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131077764 | CATATATA others(5): Show |
C | intron_variant | MODIFIER | HG02129.hp1 HG02155.hp2 NA18939.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0009 | a0001c0001t0001g0013a0001c0001t0001g0107a0001c0001t0002g0027others(8): Show | 13 | 302 | 0.0431 | -12 | c.-14 others(31): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ARHGAP39_chr8_144524179_144690846 | 144579201 | CAAAAAAA others(5): Show |
C | intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0001 | a0001c0001t0021 | a0001c0001t0021g0062 | 1 | 246 | 0.0041 | -12 | c.512 others(29): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144608156 | CAAAAAAA others(5): Show |
C | intron_variant | MODIFIER | NA19074.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0108 | 1 | 246 | 0.0041 | -12 | c.-81 others(29): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144609683 | TGAGCCAC others(5): Show |
T | intron_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0228 | 1 | 246 | 0.0041 | -12 | c.-81 others(29): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144611516 | ATAGCTCT others(5): Show |
A | intron_variant | MODIFIER | HG01074.hp2 HG01167.hp1 HG01346.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0107a0001c0001t0001g0201a0001c0001t0001g0202others(1): Show | 4 | 246 | 0.0163 | -12 | c.-81 others(29): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38601410 | GTCCTGCT others(5): Show |
G | upstream_gene_variant | MODIFIER | HG03130.hp2 | a0009 | a0009c0035 | a0009c0035t0011 | a0009c0035t0011g0124 | 1 | 350 | 0.0029 | -12 | c.-53 others(21): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 398 | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38603407 | GTCTATCT others(5): Show |
G | intron_variant | MODIFIER | HG01167.hp1 HG01243.hp2 HG01261.hp1 others(19): Show |
a0001a0005a0008others(3): Show | a0001c0001a0001c0002a0001c0004others(6): Show | a0001c0001t0002a0001c0002t0002a0001c0004t0007others(6): Show | a0001c0001t0002g0012a0001c0001t0002g0013a0001c0001t0002g0014others(16): Show | 22 | 350 | 0.0629 | -12 | c.137 others(29): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38603517 | CCATCTAT others(5): Show |
C | intron_variant | MODIFIER | HG01884.hp1 HG01891.hp2 HG02886.hp2 others(3): Show |
a0004a0005a0008 | a0004c0011a0005c0006a0008c0013 | a0004c0011t0007a0005c0006t0002a0008c0013t0008 | a0004c0011t0007g0292a0005c0006t0002g0029a0008c0013t0008g0028others(1): Show | 6 | 350 | 0.0171 | -12 | c.137 others(29): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38644613 | GTCACCCA others(5): Show |
G | intron_variant | MODIFIER | HG02258.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
a0001a0004a0021 | a0001c0002a0001c0004a0001c0008others(3): Show | a0001c0002t0004a0001c0004t0004a0001c0008t0004others(4): Show | a0001c0002t0004g0073a0001c0004t0004g0045a0001c0008t0004g0026others(7): Show | 12 | 350 | 0.0343 | -12 | c.156 others(29): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100714389 | TTGTGTGT others(5): Show |
T | intron_variant | MODIFIER | HG02698.hp1 HG04228.hp2 |
a0002 | a0002c0002 | a0002c0002t0004 | a0002c0002t0004g0268a0002c0002t0004g0278 | 2 | 286 | 0.0070 | -12 | c.154 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100728713 | CGTATATA others(5): Show |
C | intron_variant | MODIFIER | HG00408.hp2 HG00544.hp2 HG01358.hp1 others(5): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0003t0003others(2): Show | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0087others(5): Show | 8 | 286 | 0.0280 | -12 | c.154 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100728714 | GTATATAT others(5): Show |
G | intron_variant | MODIFIER | NA19077.hp2 | a0001 | a0001c0003 | a0001c0003t0006 | a0001c0003t0006g0161 | 1 | 286 | 0.0035 | -12 | c.154 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100769712 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG03017.hp2 NA20905.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0002 | a0001c0001t0002g0096a0002c0002t0002g0102 | 2 | 286 | 0.0070 | -12 | c.155 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100789531 | GGGCATGA others(5): Show |
G | intron_variant | MODIFIER | HG00408.hp2 HG00544.hp2 HG00733.hp2 others(34): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0031others(9): Show | a0001c0001t0001g0023a0001c0001t0001g0026a0001c0001t0001g0027others(34): Show | 37 | 286 | 0.1294 | -12 | c.251 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100837666 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG01346.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0149 | 1 | 286 | 0.0035 | -12 | c.313 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100841396 | GATTTCAC others(5): Show |
G | intron_variant | MODIFIER | HG03453.hp2 | a0001 | a0001c0008 | a0001c0008t0010 | a0001c0008t0010g0253 | 1 | 286 | 0.0035 | -12 | c.313 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100875073 | GTCTCTCT others(5): Show |
G | intron_variant | MODIFIER | HG02486.hp1 HG02572.hp1 HG02622.hp1 others(4): Show |
a0001a0002a0005 | a0001c0010a0002c0002a0002c0006others(1): Show | a0001c0010t0001a0002c0002t0002a0002c0006t0008others(2): Show | a0001c0010t0001g0238a0002c0002t0002g0102a0002c0006t0008g0240others(4): Show | 7 | 286 | 0.0245 | -12 | c.384 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875099 | CTCTCTCT others(5): Show |
C | intron_variant | MODIFIER | HG01515.hp2 HG03669.hp2 NA18968.hp1 |
a0001 | a0001c0001a0001c0015 | a0001c0001t0001a0001c0001t0032a0001c0015t0001 | a0001c0001t0001g0129a0001c0001t0032g0008a0001c0015t0001g0277 | 3 | 286 | 0.0105 | -12 | c.384 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875101 | CTCTCTCT others(5): Show |
C | intron_variant | MODIFIER | NA18952.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0275 | 1 | 286 | 0.0035 | -12 | c.384 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875103 | CTCTCTGT others(5): Show |
C | intron_variant | MODIFIER | HG01243.hp2 HG02145.hp2 HG02630.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0037a0002c0002t0002a0002c0002t0021others(1): Show | a0001c0001t0037g0041a0002c0002t0002g0139a0002c0002t0002g0226others(3): Show | 6 | 286 | 0.0210 | -12 | c.384 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875105 | CTCTGTGT others(5): Show |
C | intron_variant | MODIFIER | HG02897.hp1 NA19088.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002 | a0001c0001t0001g0211a0002c0002t0002g0225 | 2 | 286 | 0.0070 | -12 | c.384 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875107 | CTGTGTGT others(5): Show |
C | intron_variant | MODIFIER | HG01074.hp1 HG01109.hp1 HG01361.hp2 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0005 | a0002c0002t0002g0006a0002c0002t0005g0110a0002c0002t0005g0111others(1): Show | 4 | 286 | 0.0140 | -12 | c.384 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | AATATATA others(5): Show |
A | intron_variant | MODIFIER | HG00423.hp2 HG00738.hp2 HG03225.hp2 others(3): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0009 | a0001c0001t0001a0001c0001t0019a0001c0001t0037others(2): Show | a0001c0001t0001g0128a0001c0001t0001g0211a0001c0001t0019g0089others(3): Show | 6 | 286 | 0.0210 | -12 | c.385 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100917015 | TTGTGTGT others(5): Show |
T | intron_variant | MODIFIER | HG00408.hp2 HG00639.hp1 HG01123.hp2 others(41): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0017 | a0001c0001t0001a0001c0001t0002a0001c0001t0030others(3): Show | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0027others(41): Show | 44 | 286 | 0.1539 | -12 | c.486 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921239 | ATATATAT others(5): Show |
A | intron_variant | MODIFIER | HG01074.hp1 HG01516.hp2 HG01884.hp2 |
a0002 | a0002c0002 | a0002c0002t0005 | a0002c0002t0005g0114a0002c0002t0005g0115a0002c0002t0005g0143 | 3 | 286 | 0.0105 | -12 | c.487 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921241 | ATATATTT others(5): Show |
A | intron_variant | MODIFIER | HG01106.hp2 HG01175.hp1 HG01981.hp1 |
a0002a0003 | a0002c0002a0003c0007 | a0002c0002t0002a0003c0007t0005 | a0002c0002t0002g0019a0002c0002t0002g0147a0003c0007t0005g0059 | 3 | 286 | 0.0105 | -12 | c.487 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921243 | ATATTTTT others(5): Show |
A | intron_variant | MODIFIER | HG01261.hp2 HG02257.hp1 |
a0003 | a0003c0007 | a0003c0007t0005 | a0003c0007t0005g0058a0003c0007t0005g0061 | 2 | 286 | 0.0070 | -12 | c.487 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921245 | ATTTTTTT others(5): Show |
A | intron_variant | MODIFIER | HG04204.hp2 NA20905.hp2 |
a0001 | a0001c0003 | a0001c0003t0014 | a0001c0003t0014g0234a0001c0003t0014g0235 | 2 | 286 | 0.0070 | -12 | c.487 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG01496.hp2 NA21309.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0041a0002c0002t0025 | a0001c0001t0041g0116a0002c0002t0025g0247 | 2 | 286 | 0.0070 | -12 | c.245 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100987806 | AAAATAAA others(5): Show |
A | intron_variant | MODIFIER | HG00408.hp1 HG00597.hp2 HG00673.hp2 others(22): Show |
a0001a0002 | a0001c0003a0001c0008a0002c0005 | a0001c0003t0003a0001c0003t0022a0001c0008t0010others(2): Show | a0001c0003t0003g0118a0001c0003t0003g0119a0001c0003t0003g0155others(22): Show | 25 | 286 | 0.0874 | -12 | c.253 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12802927 | TTATATAT others(5): Show |
T | intron_variant | MODIFIER | HG02630.hp2 HG03486.hp2 NA19084.hp1 |
a0001a0002 | a0001c0003a0001c0005a0002c0007 | a0001c0003t0001a0001c0005t0001a0002c0007t0001 | a0001c0003t0001g0178a0001c0005t0001g0216a0002c0007t0001g0011 | 3 | 230 | 0.0130 | -12 | c.53+ others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12802959 | ATATATAT others(5): Show |
A | intron_variant | MODIFIER | HG00642.hp1 HG01192.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0006a0001c0002t0001 | a0001c0001t0006g0099a0001c0002t0001g0100 | 2 | 230 | 0.0087 | -12 | c.53+ others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12857765 | GTTATTTA others(5): Show |
G | intron_variant | MODIFIER | HG02809.hp2 HG02886.hp2 HG03239.hp1 others(1): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0013a0001c0001t0014others(1): Show | a0001c0001t0001g0212a0001c0001t0013g0098a0001c0001t0014g0179others(1): Show | 4 | 230 | 0.0174 | -12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12860856 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(122): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(36): Show | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0013others(122): Show | 125 | 230 | 0.5435 | -12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12868557 | CAAAAAGT others(5): Show |
C | intron_variant | MODIFIER | HG02451.hp2 HG02559.hp2 HG02647.hp1 others(5): Show |
a0001 | a0001c0001a0001c0005a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(3): Show | a0001c0001t0001g0033a0001c0001t0001g0185a0001c0001t0001g0214others(5): Show | 8 | 230 | 0.0348 | -12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12868589 | TTTTATAT others(5): Show |
T | intron_variant | MODIFIER | HG01169.hp1 HG01496.hp2 HG01891.hp2 others(19): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0163others(19): Show | 22 | 230 | 0.0957 | -12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12868591 | TTATATAT others(5): Show |
T | intron_variant | MODIFIER | HG02647.hp1 | a0001 | a0001c0011 | a0001c0011t0001 | a0001c0011t0001g0215 | 1 | 230 | 0.0044 | -12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12873918 | TAAATAAA others(5): Show |
T | intron_variant | MODIFIER | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(6): Show |
a0001 | a0001c0001a0001c0004a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(5): Show | a0001c0001t0001g0183a0001c0001t0003g0028a0001c0001t0010g0182others(6): Show | 9 | 230 | 0.0391 | -12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12873943 | AAATAAAT others(5): Show |
A | intron_variant | MODIFIER | HG02109.hp1 HG03209.hp2 HG03688.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0002t0001 | a0001c0001t0003g0075a0001c0001t0003g0076a0001c0002t0001g0119 | 3 | 230 | 0.0130 | -12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12903083 | TGAGAGAG others(5): Show |
T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(1): Show | a0001c0001t0001g0158a0001c0001t0002g0149a0001c0001t0002g0167others(4): Show | 7 | 230 | 0.0304 | -12 | c.199 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12952722 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG01106.hp2 HG01496.hp2 HG01884.hp1 others(6): Show |
a0001 | a0001c0001a0001c0003a0001c0008 | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(3): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0130others(6): Show | 9 | 230 | 0.0391 | -12 | c.113 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12991861 | TTACTTAC others(5): Show |
T | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0013 | a0001c0001t0006g0024a0001c0001t0006g0097a0001c0001t0006g0099others(7): Show | 10 | 230 | 0.0435 | -12 | c.*16 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 219 | chr17 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1073365 | TGGGTTTT others(5): Show |
T | intron_variant | MODIFIER | HG02257.hp2 | a0003 | a0003c0040 | a0003c0040t0028 | a0003c0040t0028g0144 | 1 | 418 | 0.0024 | -12 | c.565 others(25): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 3/22 | chr19 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1076483 | CTTTTTTT others(5): Show |
C | intron_variant | MODIFIER | HG00642.hp2 HG01070.hp1 HG02293.hp2 others(12): Show |
a0002a0004a0005others(2): Show | a0002c0001a0004c0005a0005c0008others(2): Show | a0002c0001t0005a0002c0001t0016a0002c0001t0025others(4): Show | a0002c0001t0005g0047a0002c0001t0005g0285a0002c0001t0005g0286others(10): Show | 15 | 418 | 0.0359 | -12 | c.118 others(31): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar |