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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP10_chr4_147727088_148077776 | 147830512 | C | CTTTT | intron_variant | MODIFIER | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(27): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0006others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0006t0001others(3): Show | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(27): Show | 30 | 106 | 0.2830 | 4 | c.312 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147839092 | G | GTATC | intron_variant | MODIFIER | HG02886.hp1 HG03098.hp1 HG03195.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0005t0001others(1): Show | a0001c0001t0001g0053a0001c0001t0001g0086a0001c0002t0001g0033others(2): Show | 5 | 106 | 0.0472 | 4 | c.313 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147839114 | A | ATCTG | intron_variant | MODIFIER | HG01884.hp2 HG03098.hp2 NA18906.hp2 |
a0001 | a0001c0002a0001c0004a0001c0006 | a0001c0002t0001a0001c0004t0001a0001c0006t0001 | a0001c0002t0001g0090a0001c0004t0001g0102a0001c0006t0001g0071 | 3 | 106 | 0.0283 | 4 | c.313 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147839138 | A | ATCTG | intron_variant | MODIFIER | HG02109.hp2 NA18906.hp1 NA19064.hp2 |
a0001a0004 | a0001c0001a0001c0002a0004c0010 | a0001c0001t0001a0001c0002t0001a0004c0010t0001 | a0001c0001t0001g0046a0001c0002t0001g0029a0004c0010t0001g0048 | 3 | 106 | 0.0283 | 4 | c.313 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147839142 | A | ATCTG | intron_variant | MODIFIER | HG00558.hp2 HG01169.hp2 HG02080.hp1 others(11): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0008others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0008t0001others(2): Show | a0001c0001t0001g0010a0001c0001t0001g0026a0001c0001t0001g0030others(11): Show | 14 | 106 | 0.1321 | 4 | c.313 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147869996 | G | GTTTT | intron_variant | MODIFIER | HG01891.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(3): Show | a0001c0001t0001g0015a0001c0001t0001g0050a0001c0001t0001g0083others(7): Show | 10 | 106 | 0.0943 | 4 | c.702 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147869998 | T | TTTTG | intron_variant | MODIFIER | HG02615.hp1 HG02886.hp2 HG02976.hp2 others(1): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0001 | a0001c0001t0001g0035a0001c0001t0001g0043a0001c0001t0001g0080others(1): Show | 4 | 106 | 0.0377 | 4 | c.702 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147870928 | C | CTGTG | intron_variant | MODIFIER | HG02055.hp2 HG02145.hp1 HG02572.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(3): Show | a0001c0001t0001g0035a0001c0001t0001g0043a0001c0001t0001g0051others(10): Show | 13 | 106 | 0.1226 | 4 | c.703 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147873681 | A | AACAC | intron_variant | MODIFIER | HG02896.hp2 HG03209.hp2 NA19043.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0014a0001c0001t0001g0047a0001c0001t0001g0062others(1): Show | 4 | 106 | 0.0377 | 4 | c.703 others(21): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147911992 | C | CATAT | intron_variant | MODIFIER | HG02080.hp2 HG02895.hp1 HG03098.hp2 others(5): Show |
a0001 | a0001c0001a0001c0004a0001c0005 | a0001c0001t0001a0001c0004t0001a0001c0005t0001 | a0001c0001t0001g0006a0001c0001t0001g0030a0001c0001t0001g0036others(5): Show | 8 | 106 | 0.0755 | 4 | c.116 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147917839 | G | GTCTT | intron_variant | MODIFIER | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(40): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(6): Show | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0014others(40): Show | 43 | 106 | 0.4057 | 4 | c.122 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147969345 | T | TTTTG | intron_variant | MODIFIER | HG01993.hp1 HG02738.hp1 HG02895.hp2 others(5): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0002c0003t0001 | a0001c0001t0001g0002a0001c0001t0001g0037a0001c0001t0001g0049others(5): Show | 8 | 106 | 0.0755 | 4 | c.171 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147982546 | C | CTTTT | intron_variant | MODIFIER | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(15): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0001a0001c0002t0001a0001c0004t0001others(4): Show | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0022others(15): Show | 18 | 106 | 0.1698 | 4 | c.171 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148017652 | C | CTATA | intron_variant | MODIFIER | HG02056.hp2 HG02145.hp1 HG02615.hp1 others(10): Show |
a0001 | a0001c0001a0001c0005a0001c0006 | a0001c0001t0001a0001c0005t0001a0001c0006t0001 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0038others(10): Show | 13 | 106 | 0.1226 | 4 | c.171 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148036066 | C | CTGTG | intron_variant | MODIFIER | HG00558.hp1 HG00558.hp2 HG01071.hp1 others(30): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0005others(6): Show | a0001c0001t0001a0001c0002t0001a0001c0005t0001others(6): Show | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0025others(30): Show | 33 | 106 | 0.3113 | 4 | c.186 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148043614 | A | AATAT | intron_variant | MODIFIER | HG02145.hp1 HG02896.hp2 HG03492.hp2 others(1): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0006t0001 | a0001c0001t0001g0036a0001c0001t0001g0047a0001c0001t0001g0097others(1): Show | 4 | 106 | 0.0377 | 4 | c.186 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148043746 | G | GTATA | intron_variant | MODIFIER | HG00558.hp2 HG01167.hp1 HG01169.hp1 others(25): Show |
a0001a0002a0003 | a0001c0001a0001c0006a0001c0011others(2): Show | a0001c0001t0001a0001c0006t0001a0001c0011t0001others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0026others(25): Show | 28 | 106 | 0.2642 | 4 | c.186 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148049795 | G | GTTTT | intron_variant | MODIFIER | HG01884.hp2 HG01993.hp1 HG02165.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0009 | a0001c0001t0001a0001c0002t0001a0001c0009t0001 | a0001c0001t0001g0037a0001c0002t0001g0019a0001c0002t0001g0021others(6): Show | 9 | 106 | 0.0849 | 4 | c.202 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148059973 | T | TGAGA | intron_variant | MODIFIER | HG02080.hp1 NA18983.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0056a0001c0002t0001g0013 | 2 | 106 | 0.0189 | 4 | c.202 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148065979 | C | CAAAA | intron_variant | MODIFIER | HG00558.hp1 HG00558.hp2 HG01070.hp1 others(31): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(4): Show | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0015others(31): Show | 34 | 106 | 0.3208 | 4 | c.227 others(23): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP11A_chr15_32610504_32644941 | 32610719 | C | CAAAT | upstream_gene_variant | MODIFIER | HG00738.hp2 HG01099.hp1 HG01433.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0014a0001c0001t0001g0104a0001c0001t0002g0003others(5): Show | 10 | 335 | 0.0299 | 4 | c.-54 others(15): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 4784 | chr15 | TogoVar | ||||||
ARHGAP11A_chr15_32610504_32644941 | 32613813 | C | CAAAA | upstream_gene_variant | MODIFIER | HG00323.hp2 HG00438.hp2 HG00558.hp2 others(107): Show |
a0001a0005 | a0001c0001a0001c0003a0001c0012others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0014others(59): Show | 110 | 335 | 0.3284 | 4 | c.-23 others(15): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 1690 | chr15 | TogoVar | ||||||
ARHGAP11A_chr15_32610504_32644941 | 32629941 | A | AGTGT | intron_variant | MODIFIER | HG00323.hp2 HG00558.hp2 HG00639.hp1 others(53): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0015others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(8): Show | a0001c0001t0001g0001a0001c0001t0001g0021a0001c0001t0001g0027others(29): Show | 56 | 335 | 0.1672 | 4 | c.110 others(21): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
ARHGAP11B_chr15_30621128_30643810 | 30621327 | C | CAAAT | upstream_gene_variant | MODIFIER | HG01081.hp1 HG01123.hp2 HG01261.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0003 | 4 | 247 | 0.0162 | 4 | c.-54 others(15): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 4800 | chr15 | TogoVar | ||||||
ARHGAP11B_chr15_30621128_30643810 | 30639971 | A | AGTGT | downstream_gene_variant | MODIFIER | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(32): Show |
a0001a0005 | a0001c0001a0005c0004 | a0001c0001t0001a0001c0001t0005a0005c0004t0001 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(17): Show | 35 | 247 | 0.1417 | 4 | c.*12 others(15): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1162 | chr15 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31804673 | C | CTTTT | downstream_gene_variant | MODIFIER | HG00673.hp2 HG01106.hp1 HG01175.hp2 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(1): Show | a0001c0001t0001g0110a0001c0001t0001g0213a0001c0001t0001g0228others(11): Show | 14 | 322 | 0.0435 | 4 | c.*29 others(15): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 724 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31805648 | T | TCACA | 3_prime_UTR_variant | MODIFIER | HG00099.hp1 HG00544.hp2 HG00597.hp2 others(76): Show |
a0001 | a0001c0001a0001c0011 | a0001c0001t0001a0001c0001t0013a0001c0001t0019others(6): Show | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0088others(76): Show | 79 | 322 | 0.2453 | 4 | c.*20 others(15): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2009 | chr10 | TogoVar | |||||
ARHGAP12_chr10_31800398_31933831 | 31816168 | C | CGTGT | intron_variant | MODIFIER | HG00735.hp1 HG01346.hp2 HG01358.hp1 others(26): Show |
a0001a0002a0005 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(12): Show | a0001c0001t0001g0114a0001c0001t0001g0137a0001c0001t0001g0146others(26): Show | 29 | 322 | 0.0901 | 4 | c.173 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31862705 | G | GACAC | intron_variant | MODIFIER | HG01934.hp1 HG02273.hp2 HG02735.hp1 others(6): Show |
a0001a0004 | a0001c0001a0004c0012 | a0001c0001t0003a0001c0001t0022a0004c0012t0003 | a0001c0001t0003g0170a0001c0001t0003g0171a0001c0001t0003g0189others(6): Show | 9 | 322 | 0.0280 | 4 | c.685 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31874973 | C | CAAAA | intron_variant | MODIFIER | HG00673.hp1 HG01106.hp2 HG01123.hp2 others(26): Show |
a0001a0002a0003 | a0001c0007a0002c0002a0003c0004 | a0001c0007t0028a0002c0002t0002a0002c0002t0007others(5): Show | a0001c0007t0028g0240a0002c0002t0002g0252a0002c0002t0002g0261others(26): Show | 29 | 322 | 0.0901 | 4 | c.685 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31901768 | C | CTCTT | intron_variant | MODIFIER | HG00735.hp2 HG02257.hp2 HG02451.hp1 others(13): Show |
a0001 | a0001c0003a0001c0005a0001c0014 | a0001c0003t0010a0001c0003t0016a0001c0003t0027others(3): Show | a0001c0003t0010g0005a0001c0003t0010g0006a0001c0003t0010g0009others(13): Show | 16 | 322 | 0.0497 | 4 | c.684 others(21): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31918315 | T | TCACA | intron_variant | MODIFIER | HG01175.hp2 HG01192.hp1 HG01258.hp1 others(16): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(5): Show | a0001c0001t0001g0113a0001c0001t0001g0143a0001c0001t0001g0226others(16): Show | 19 | 322 | 0.0590 | 4 | c.-11 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31920449 | C | CAAAA | intron_variant | MODIFIER | HG00597.hp1 HG00621.hp1 HG01978.hp2 others(10): Show |
a0001a0002a0003 | a0001c0001a0001c0007a0001c0010others(2): Show | a0001c0001t0004a0001c0007t0028a0001c0010t0053others(3): Show | a0001c0001t0004g0044a0001c0007t0028g0239a0001c0007t0028g0240others(10): Show | 13 | 322 | 0.0404 | 4 | c.-11 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31923132 | G | GAAAA | intron_variant | MODIFIER | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(83): Show |
a0001a0002a0003 | a0001c0001a0001c0006a0001c0007others(2): Show | a0001c0001t0004a0001c0001t0005a0001c0001t0023others(12): Show | a0001c0001t0004g0019a0001c0001t0004g0020a0001c0001t0004g0021others(83): Show | 86 | 322 | 0.2671 | 4 | c.-11 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31923152 | A | AAAAC | intron_variant | MODIFIER | HG02257.hp1 HG02559.hp1 HG02622.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0009a0001c0001t0044a0001c0001t0045 | a0001c0001t0009g0032a0001c0001t0009g0072a0001c0001t0009g0077others(6): Show | 9 | 322 | 0.0280 | 4 | c.-11 others(23): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31931872 | C | CAAAT | upstream_gene_variant | MODIFIER | HG00099.hp2 HG00738.hp1 HG00741.hp1 others(22): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(3): Show | a0001c0001t0001g0215a0001c0001t0001g0217a0001c0001t0001g0218others(22): Show | 25 | 322 | 0.0776 | 4 | c.-33 others(15): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 3042 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31933207 | C | CATAT | upstream_gene_variant | MODIFIER | HG01175.hp2 HG01192.hp1 HG01515.hp1 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0012others(5): Show | a0001c0001t0001g0083a0001c0001t0001g0102a0001c0001t0001g0110others(13): Show | 16 | 322 | 0.0497 | 4 | c.-46 others(15): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4377 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31933240 | A | ATATC | upstream_gene_variant | MODIFIER | HG02717.hp1 HG02970.hp2 HG03225.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0011a0001c0001t0017 | a0001c0001t0011g0058a0001c0001t0011g0059a0001c0001t0017g0050others(2): Show | 5 | 322 | 0.0155 | 4 | c.-46 others(15): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4410 | chr10 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143134104 | A | AATCT | intron_variant | MODIFIER | HG00741.hp1 NA18612.hp1 NA21309.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0004a0001c0001t0001g0094a0001c0002t0001g0093 | 3 | 162 | 0.0185 | 4 | c.-15 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143165948 | A | AAGAG | intron_variant | MODIFIER | HG01261.hp1 HG02109.hp1 HG03225.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0039a0001c0001t0001g0069a0001c0001t0001g0096others(1): Show | 4 | 162 | 0.0247 | 4 | c.165 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143165960 | G | GAGAA | intron_variant | MODIFIER | HG01496.hp2 HG02698.hp1 HG03490.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0014a0001c0001t0001g0058a0001c0001t0001g0076others(3): Show | 6 | 162 | 0.0370 | 4 | c.165 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143165997 | A | AGAAG | intron_variant | MODIFIER | HG00609.hp2 HG01255.hp1 HG02145.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0053others(3): Show | 6 | 162 | 0.0370 | 4 | c.165 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143166041 | A | AAAAG | intron_variant | MODIFIER | HG00621.hp1 HG00621.hp2 HG01069.hp2 others(48): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0002t0001a0002c0004t0001others(1): Show | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0008others(48): Show | 51 | 162 | 0.3148 | 4 | c.165 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143179891 | C | CAAAA | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp2 HG01069.hp1 others(40): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(40): Show | 43 | 162 | 0.2654 | 4 | c.166 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143194709 | C | CTGTT | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(137): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(137): Show | 140 | 162 | 0.8642 | 4 | c.166 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143197967 | T | TACAC | intron_variant | MODIFIER | HG00609.hp2 HG00741.hp1 HG01261.hp2 others(18): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0003t0001 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0024others(18): Show | 21 | 162 | 0.1296 | 4 | c.166 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143200425 | G | GATCT | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG01071.hp2 others(29): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0021others(29): Show | 32 | 162 | 0.1975 | 4 | c.166 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143209557 | T | TAAAA | intron_variant | MODIFIER | HG02109.hp2 HG02523.hp1 HG03098.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0062others(2): Show | 5 | 162 | 0.0309 | 4 | c.235 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143215279 | C | CTTGT | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG01071.hp2 others(31): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0021others(31): Show | 34 | 162 | 0.2099 | 4 | c.235 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143239990 | C | CAAAA | intron_variant | MODIFIER | HG02074.hp2 HG03195.hp2 NA18953.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0025a0001c0001t0001g0035a0001c0001t0001g0072others(2): Show | 5 | 162 | 0.0309 | 4 | c.385 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |