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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP6_chrX_11132544_11670920 | 11176300 | CATATATA others(23): Show |
C | intron_variant | MODIFIER | NA18962.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0040 | 1 | 144 | 0.0069 | -30 | c.162 others(49): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11590775 | CGAAAAGA others(23): Show |
C | intron_variant | MODIFIER | NA18990.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0120 | 1 | 144 | 0.0069 | -30 | c.588 others(49): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11660530 | CAAAAAAA others(23): Show |
C | intron_variant | MODIFIER | HG02965.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0043 | 1 | 144 | 0.0069 | -30 | c.588 others(47): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1832793 | CAGAGGCA others(23): Show |
C | 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 | -30 | c.-48 others(47): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1887621 | TTGTGAGG others(23): Show |
T | intron_variant | MODIFIER | HG00597.hp1 HG00673.hp2 HG01496.hp1 others(31): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(20): Show | a0001c0001t0004a0001c0001t0043a0001c0002t0001others(23): Show | a0001c0001t0004g0138a0001c0001t0043g0145a0001c0002t0001g0048others(31): Show | 34 | 363 | 0.0937 | -30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1888104 | TGAGGAGA others(23): Show |
T | intron_variant | MODIFIER | NA18949.hp1 NA18963.hp2 NA18970.hp1 |
a0002 | a0002c0031a0002c0033 | a0002c0031t0001a0002c0033t0001 | a0002c0031t0001g0188a0002c0031t0001g0273a0002c0033t0001g0257 | 3 | 363 | 0.0083 | -30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1888124 | TGAGGGTT others(23): Show |
T | intron_variant | MODIFIER | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(29): Show |
a0002a0008a0017 | a0002c0017a0002c0022a0002c0024others(19): Show | a0002c0017t0002a0002c0017t0006a0002c0022t0001others(23): Show | a0002c0017t0002g0041a0002c0017t0002g0042a0002c0017t0002g0056others(28): Show | 32 | 363 | 0.0882 | -30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1888159 | GTTGCGAG others(23): Show |
G | intron_variant | MODIFIER | HG02630.hp2 HG02647.hp1 HG03834.hp2 |
a0001 | a0001c0005a0001c0140a0001c0157 | a0001c0005t0031a0001c0140t0005a0001c0157t0006 | a0001c0005t0031g0351a0001c0140t0005g0297a0001c0157t0006g0093 | 3 | 363 | 0.0083 | -30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1888183 | TGAGGGTT others(23): Show |
T | intron_variant | MODIFIER | HG02486.hp2 HG03209.hp1 |
a0004a0023 | a0004c0044a0023c0089 | a0004c0044t0004a0023c0089t0034 | a0004c0044t0004g0349a0023c0089t0034g0350 | 2 | 363 | 0.0055 | -30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1888992 | GGTCTACA others(23): Show |
G | intron_variant | MODIFIER | HG01975.hp2 | a0002 | a0002c0025 | a0002c0025t0024 | a0002c0025t0024g0106 | 1 | 363 | 0.0028 | -30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1889523 | GGTATTGA others(23): Show |
G | intron_variant | MODIFIER | HG00597.hp2 HG01943.hp1 HG01993.hp2 others(18): Show |
a0001a0006a0007others(1): Show | a0001c0001a0001c0007a0001c0010others(15): Show | a0001c0001t0012a0001c0007t0001a0001c0010t0001others(16): Show | a0001c0001t0012g0207a0001c0007t0001g0323a0001c0010t0001g0182others(18): Show | 21 | 363 | 0.0579 | -30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1889845 | AGGTTTGT others(23): Show |
A | intron_variant | MODIFIER | HG02451.hp2 HG02922.hp2 |
a0012a0020 | a0012c0130a0020c0103 | a0012c0130t0073a0020c0103t0002 | a0012c0130t0073g0342a0020c0103t0002g0039 | 2 | 363 | 0.0055 | -30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1890130 | GGAGTGGG others(23): Show |
G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0002a0001c0003others(113): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(171): Show | a0001c0001t0002g0053a0001c0001t0002g0066a0001c0001t0002g0224others(241): Show | 245 | 363 | 0.6749 | -30 | c.118 others(49): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 157035894 | AATATATA others(23): Show |
A | intron_variant | MODIFIER | HG03098.hp1 | a0010 | a0010c0014 | a0010c0014t0014 | a0010c0014t0014g0205 | 1 | 362 | 0.0028 | -30 | c.32+ others(45): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157035950 | AATATATA others(23): Show |
A | intron_variant | MODIFIER | HG02109.hp2 | a0002 | a0002c0004 | a0002c0004t0005 | a0002c0004t0005g0020 | 1 | 362 | 0.0028 | -30 | c.32+ others(45): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157036006 | AATATATA others(23): Show |
A | intron_variant | MODIFIER | HG02723.hp2 HG02809.hp1 HG02922.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0122a0001c0001t0006g0123a0001c0001t0006g0124others(1): Show | 4 | 362 | 0.0111 | -30 | c.32+ others(45): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120351427 | ATATATAT others(23): Show |
A | intron_variant | MODIFIER | HG00621.hp2 HG01074.hp1 HG01978.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0140a0001c0001t0001g0148a0001c0001t0001g0152others(7): Show | 10 | 308 | 0.0325 | -30 | c.32+ others(47): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120351429 | ATATATAT others(23): Show |
A | intron_variant | MODIFIER | HG02602.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0171 | 1 | 308 | 0.0033 | -30 | c.32+ others(47): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120351437 | ATATATAT others(23): Show |
A | intron_variant | MODIFIER | HG02572.hp2 | a0008 | a0008c0014 | a0008c0014t0019 | a0008c0014t0019g0011 | 1 | 308 | 0.0033 | -30 | c.32+ others(47): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF17_chr11_73303276_73374388 | 73332379 | GTGTGTGT others(23): Show |
G | intron_variant | MODIFIER | HG01081.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0113 | 1 | 228 | 0.0044 | -30 | c.319 others(51): Show |
ARHGEF17 | ENSG00000110237.5 | transcript | ENST00000263674.4 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7350763 | GGTGGGTG others(23): Show |
G | intron_variant | MODIFIER | HG02895.hp1 | a0023 | a0023c0041 | a0023c0041t0002 | a0023c0041t0002g0298 | 1 | 298 | 0.0034 | -30 | c.-11 others(49): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7362011 | AAGAAGGA others(23): Show |
A | intron_variant | MODIFIER | HG01074.hp1 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0151 | 1 | 298 | 0.0034 | -30 | c.-11 others(47): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7362143 | GAGAAGGA others(23): Show |
G | intron_variant | MODIFIER | HG01496.hp1 HG02040.hp1 NA18998.hp2 others(1): Show |
a0001a0004a0006 | a0001c0002a0004c0015a0006c0008 | a0001c0002t0002a0001c0002t0003a0004c0015t0003others(1): Show | a0001c0002t0002g0129a0001c0002t0003g0135a0004c0015t0003g0166others(1): Show | 4 | 298 | 0.0134 | -30 | c.-11 others(47): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7385873 | CCCCTCCC others(23): Show |
C | intron_variant | MODIFIER | HG01106.hp2 NA18942.hp1 |
a0001 | a0001c0019a0001c0021 | a0001c0019t0006a0001c0021t0006 | a0001c0019t0006g0078a0001c0021t0006g0059 | 2 | 298 | 0.0067 | -30 | c.967 others(47): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7385885 | TCCCTCCC others(23): Show |
T | intron_variant | MODIFIER | HG03834.hp1 NA18973.hp2 |
a0001a0018 | a0001c0019a0018c0053 | a0001c0019t0006a0018c0053t0001 | a0001c0019t0006g0063a0018c0053t0001g0236 | 2 | 298 | 0.0067 | -30 | c.967 others(47): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7419949 | TCACACTC others(23): Show |
T | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(81): Show |
a0001a0002a0004others(17): Show | a0001c0001a0001c0002a0001c0013others(32): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0030others(37): Show | a0001c0001t0002g0012a0001c0001t0002g0070a0001c0001t0002g0144others(81): Show | 84 | 298 | 0.2819 | -30 | c.968 others(49): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73671694 | TTATATAT others(23): Show |
T | intron_variant | MODIFIER | HG00621.hp2 HG00738.hp2 HG02257.hp2 others(1): Show |
a0001a0005a0013 | a0001c0001a0001c0023a0005c0008others(1): Show | a0001c0001t0001a0001c0023t0001a0005c0008t0001others(1): Show | a0001c0001t0001g0038a0001c0023t0001g0034a0005c0008t0001g0017others(1): Show | 4 | 188 | 0.0213 | -30 | c.-11 others(49): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73671710 | ATATATAT others(23): Show |
A | intron_variant | MODIFIER | HG00280.hp1 NA18962.hp2 |
a0003a0005 | a0003c0005a0005c0008 | a0003c0005t0001a0005c0008t0002 | a0003c0005t0001g0029a0005c0008t0002g0037 | 2 | 188 | 0.0106 | -30 | c.-11 others(49): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73671712 | ATATATAT others(23): Show |
A | intron_variant | MODIFIER | HG02074.hp1 NA18995.hp2 |
a0005a0029 | a0005c0008a0029c0074 | a0005c0008t0002a0029c0074t0001 | a0005c0008t0002g0006a0029c0074t0001g0177 | 2 | 188 | 0.0106 | -30 | c.-11 others(49): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73671714 | ATATATAT others(23): Show |
A | intron_variant | MODIFIER | HG00408.hp2 HG00438.hp2 HG01517.hp2 others(13): Show |
a0001a0002a0003others(8): Show | a0001c0001a0002c0003a0003c0005others(9): Show | a0001c0001t0002a0002c0003t0001a0002c0003t0002others(10): Show | a0001c0001t0002g0050a0001c0001t0002g0058a0001c0001t0002g0062others(13): Show | 16 | 188 | 0.0851 | -30 | c.-11 others(49): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73671716 | ATATATAT others(23): Show |
A | intron_variant | MODIFIER | NA18975.hp1 | a0038 | a0038c0053 | a0038c0053t0001 | a0038c0053t0001g0044 | 1 | 188 | 0.0053 | -30 | c.-11 others(49): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 1/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73737439 | CTTCTTTT others(23): Show |
C | intron_variant | MODIFIER | HG00280.hp2 HG00408.hp1 HG01069.hp1 others(6): Show |
a0002a0004a0006others(3): Show | a0002c0002a0002c0006a0004c0004others(6): Show | a0002c0002t0002a0002c0006t0004a0004c0004t0001others(6): Show | a0002c0002t0002g0158a0002c0006t0004g0109a0004c0004t0001g0170others(6): Show | 9 | 188 | 0.0479 | -30 | c.34- others(47): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73741371 | GTGTGTGT others(23): Show |
G | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0011a0001c0001t0002g0012 | 2 | 188 | 0.0106 | -30 | c.34- others(45): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73741379 | GTGTGTGT others(23): Show |
G | intron_variant | MODIFIER | HG03017.hp1 NA18962.hp1 |
a0024a0033 | a0024c0040a0033c0067 | a0024c0040t0004a0033c0067t0001 | a0024c0040t0004g0116a0033c0067t0001g0056 | 2 | 188 | 0.0106 | -30 | c.34- others(45): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF28_chr5_73621196_73946990 | 73741385 | GTATATAT others(23): Show |
G | intron_variant | MODIFIER | HG01169.hp1 | a0002 | a0002c0006 | a0002c0006t0003 | a0002c0006t0003g0111 | 1 | 188 | 0.0053 | -30 | c.34- others(45): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF33_chr2_38884875_38980454 | 38934557 | CCTCCCGC others(23): Show |
C | intron_variant | MODIFIER | HG01069.hp1 HG01361.hp1 NA19012.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0015 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0003t0015g0173 | 3 | 278 | 0.0108 | -30 | c.506 others(47): Show |
ARHGEF33 | ENSG00000214694.13 | transcript | ENST00000409978.7 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGEF37_chr5_149576498_149639968 | 149598348 | TTCTTCTT others(23): Show |
T | intron_variant | MODIFIER | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(30): Show |
a0001a0002a0004others(2): Show | a0001c0002a0002c0001a0004c0010others(2): Show | a0001c0002t0005a0001c0002t0006a0001c0002t0008others(10): Show | a0001c0002t0005g0370a0001c0002t0006g0083a0001c0002t0006g0088others(28): Show | 33 | 394 | 0.0838 | -30 | c.186 others(45): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105561419 | AGAATGGA others(23): Show |
A | intron_variant | MODIFIER | HG01884.hp2 | a0001 | a0001c0018 | a0001c0018t0006 | a0001c0018t0006g0026 | 1 | 186 | 0.0054 | -30 | c.196 others(47): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105561424 | GGAATAGA others(23): Show |
G | intron_variant | MODIFIER | HG01516.hp1 HG02145.hp1 |
a0003a0008 | a0003c0005a0008c0022 | a0003c0005t0004a0008c0022t0001 | a0003c0005t0004g0136a0008c0022t0001g0133 | 2 | 186 | 0.0108 | -30 | c.196 others(47): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGEF4_chr2_130831914_131052253 | 130833367 | GAAGGAAG others(23): Show |
G | upstream_gene_variant | MODIFIER | HG02615.hp1 | a0017 | a0017c0051 | a0017c0051t0006 | a0017c0051t0006g0069 | 1 | 144 | 0.0069 | -30 | c.-35 others(41): Show |
ARHGEF4 | ENSG00000136002.21 | transcript | ENST00000409359.7 | protein_coding | 3546 | chr2 | TogoVar | ||||||
ARHGEF5_chr7_144350402_144385632 | 144354828 | ACAACAAC others(23): Show |
A | upstream_gene_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(2): Show |
a0003a0004 | a0003c0012a0004c0003 | a0003c0012t0002a0004c0003t0001 | a0003c0012t0002g0006a0004c0003t0001g0002 | 5 | 288 | 0.0174 | -30 | c.-68 others(39): Show |
ARHGEF5 | ENSG00000050327.15 | transcript | ENST00000056217.10 | protein_coding | 573 | chr7 | TogoVar | ||||||
ARHGEF6_chrX_136660550_136785932 | 136726299 | CCATTATC others(23): Show |
C | intron_variant | MODIFIER | NA18964.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023 | 1 | 247 | 0.0041 | -30 | c.732 others(47): Show |
ARHGEF6 | ENSG00000129675.16 | transcript | ENST00000250617.7 | protein_coding | 6/21 | chrX | TogoVar | ||||||
ARHGEF7_chr13_111110310_111310732 | 111133763 | TTATATAT others(23): Show |
T | intron_variant | MODIFIER | HG02015.hp1 HG02132.hp2 HG02280.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0009 | a0001c0001t0001a0001c0001t0002a0001c0001t0012others(2): Show | a0001c0001t0001g0039a0001c0001t0001g0068a0001c0001t0002g0164others(9): Show | 12 | 274 | 0.0438 | -30 | c.165 others(49): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111221493 | ATATATAT others(23): Show |
A | intron_variant | MODIFIER | HG01243.hp1 homoSapiens_chm13v2.hp1 |
a0001 | a0001c0005 | a0001c0005t0020 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | 274 | 0.0073 | -30 | c.670 others(47): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARHGEF7_chr13_111110310_111310732 | 111221551 | CTATATAT others(23): Show |
C | intron_variant | MODIFIER | HG01243.hp1 homoSapiens_chm13v2.hp1 |
a0001 | a0001c0005 | a0001c0005t0020 | a0001c0005t0020g0117a0001c0005t0020g0118 | 2 | 274 | 0.0073 | -30 | c.670 others(47): Show |
ARHGEF7 | ENSG00000102606.20 | transcript | ENST00000646102.2 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156897215 | GCTGCTTC others(23): Show |
G | intron_variant | MODIFIER | HG02257.hp1 NA19240.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0078a0001c0002t0001g0077 | 2 | 150 | 0.0133 | -30 | c.198 others(49): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156934912 | TTATATAT others(23): Show |
T | intron_variant | MODIFIER | HG01109.hp1 HG01261.hp2 HG01515.hp2 others(15): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0002a0003c0010others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0001others(8): Show | a0001c0001t0001g0017a0001c0001t0001g0035a0001c0001t0001g0038others(15): Show | 18 | 150 | 0.1200 | -30 | c.213 others(47): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 156961446 | AGCCTTGG others(23): Show |
A | intron_variant | MODIFIER | HG03195.hp2 | a0002 | a0002c0014 | a0002c0014t0002 | a0002c0014t0002g0029 | 1 | 150 | 0.0067 | -30 | c.224 others(51): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARID1B_chr6_156772378_157215779 | 157039664 | TCCTTCCT others(23): Show |
T | intron_variant | MODIFIER | HG01496.hp2 HG02717.hp1 HG03195.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0003 | a0001c0001t0001g0065a0001c0001t0001g0093a0001c0002t0003g0064 | 3 | 150 | 0.0200 | -30 | c.224 others(51): Show |
ARID1B | ENSG00000049618.25 | transcript | ENST00000636930.2 | protein_coding | 4/19 | chr6 | TogoVar | ||||||
ARL15_chr5_53878942_54315573 | 53979829 | TTGTGTGT others(23): Show |
T | intron_variant | MODIFIER | NA20752.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0070 | 1 | 206 | 0.0049 | -30 | c.463 others(49): Show |
ARL15 | ENSG00000185305.12 | transcript | ENST00000504924.6 | protein_coding | 4/4 | chr5 | TogoVar |