view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
RAE1_chr20_57346255_57384202 | 57350874 | GGGGGGCG others(8): Show |
G | upstream_gene_variant | MODIFIER | HG01358.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0006 | 1 | 342 | 0.0029 | -15 | c.-55 others(24): Show |
RAE1 | ENSG00000101146.13 | transcript | ENST00000395841.7 | protein_coding | 380 | chr20 | TogoVar | |||||||
RAET1G_chr6_149911878_149928121 | 149923080 | TGTCTGAA others(8): Show |
T | 5_prime_UTR_variant | MODIFIER | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(169): Show |
a0001a0002a0006others(2): Show | a0001c0001a0001c0003a0001c0007others(6): Show | a0001c0001t0002a0001c0001t0003a0001c0003t0002others(7): Show | a0001c0001t0002g0017 a0001c0001t0002g0024 a0001c0001t0002g0043 others(22): Show |
172 | 456 | 0.3772 | -15 | c.-85 others(22): Show |
RAET1G | ENSG00000203722.8 | transcript | ENST00000367360.7 | protein_coding | 1/5 | 71 | chr6 | TogoVar | ||||||
RAF1_chr3_12578601_12669117 | 12635318 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01175.hp2 others(2): Show |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0001 a0001c0002t0001g0043 a0001c0002t0001g0045 others(1): Show |
5 | 262 | 0.0191 | -15 | c.-26 others(34): Show |
RAF1 | ENSG00000132155.14 | transcript | ENST00000251849.9 | protein_coding | 1/16 | chr3 | TogoVar | |||||||
RAF1_chr3_12578601_12669117 | 12662338 | TAAAAAAA others(8): Show |
T | intron_variant | MODIFIER | HG02280.hp2 HG02622.hp2 HG02970.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0255 a0001c0001t0005g0256 a0001c0001t0005g0257 others(2): Show |
5 | 262 | 0.0191 | -15 | c.-27 others(32): Show |
RAF1 | ENSG00000132155.14 | transcript | ENST00000251849.9 | protein_coding | 1/16 | chr3 | TogoVar | |||||||
RAI14_chr5_34651328_34837612 | 34799524 | ACACACAC others(8): Show |
A | intron_variant | MODIFIER | HG01070.hp2 HG01071.hp1 HG02572.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0003t0003a0002c0002t0002 | a0001c0001t0001g0126 a0001c0001t0001g0220 a0001c0001t0001g0248 others(3): Show |
6 | 254 | 0.0236 | -15 | c.256 others(32): Show |
RAI14 | ENSG00000039560.14 | transcript | ENST00000265109.8 | protein_coding | 4/17 | chr5 | TogoVar | |||||||
RAI14_chr5_34651328_34837612 | 34822664 | CTTTTTTT others(8): Show |
C | intron_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0238 | 1 | 254 | 0.0039 | -15 | c.111 others(32): Show |
RAI14 | ENSG00000039560.14 | transcript | ENST00000265109.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
RAI1_chr17_17676458_17816453 | 17716707 | GTGTGTCT others(8): Show |
G | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(170): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0017a0001c0019others(26): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(38): Show | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0021 others(169): Show |
173 | 252 | 0.6865 | -15 | c.-14 others(34): Show |
RAI1 | ENSG00000108557.20 | transcript | ENST00000353383.6 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RAI1_chr17_17676458_17816453 | 17793779 | CCAGCAGC others(8): Show |
C | disruptive_inframe_deletion | MODERATE | HG02055.hp2 | a0011 | a0011c0031 | a0011c0031t0002 | a0011c0031t0002g0244 | 1 | 252 | 0.0040 | -15 | c.858 others(22): Show |
p.Gln others(13): Show |
RAI1 | ENSG00000108557.20 | transcript | ENST00000353383.6 | protein_coding | 3/6 | 1342/7677 | 858/5721 | 286/1906 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||
RAI1_chr17_17676458_17816453 | 17808409 | ATTTTATT others(8): Show |
A | intron_variant | MODIFIER | HG00423.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0175 | 1 | 252 | 0.0040 | -15 | c.566 others(32): Show |
RAI1 | ENSG00000108557.20 | transcript | ENST00000353383.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RAI1_chr17_17676458_17816453 | 17808414 | ATTATTTT others(8): Show |
A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(3): Show |
a0002a0004 | a0002c0002a0002c0012a0004c0004 | a0002c0002t0002a0002c0012t0003a0002c0012t0004others(1): Show | a0002c0002t0002g0229 a0002c0012t0003g0216 a0002c0012t0004g0214 others(3): Show |
6 | 252 | 0.0238 | -15 | c.566 others(32): Show |
RAI1 | ENSG00000108557.20 | transcript | ENST00000353383.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RALA_chr7_39618572_39713120 | 39671439 | CTGTGGAC others(8): Show |
C | intron_variant | MODIFIER | NA18960.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0212 | 1 | 366 | 0.0027 | -15 | c.-37 others(34): Show |
RALA | ENSG00000006451.8 | transcript | ENST00000005257.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
RALBP1_chr18_9470513_9543114 | 9500016 | CTCGCTCT others(8): Show |
C | intron_variant | MODIFIER | HG02683.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0307 | 1 | 362 | 0.0028 | -15 | c.-55 others(34): Show |
RALBP1 | ENSG00000017797.13 | transcript | ENST00000383432.8 | protein_coding | 1/9 | chr18 | TogoVar | |||||||
RALGAPA1_chr14_35533356_35814295 | 35629948 | GTAAACTA others(8): Show |
G | intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0261 | 1 | 272 | 0.0037 | -15 | c.599 others(34): Show |
RALGAPA1 | ENSG00000174373.17 | transcript | ENST00000680220.1 | protein_coding | 33/41 | chr14 | TogoVar | |||||||
RALGAPA1_chr14_35533356_35814295 | 35707664 | TGAGAAAA others(8): Show |
T | intron_variant | MODIFIER | NA18988.hp2 | a0002 | a0002c0001 | a0002c0001t0001 | a0002c0001t0001g0087 | 1 | 272 | 0.0037 | -15 | c.226 others(34): Show |
RALGAPA1 | ENSG00000174373.17 | transcript | ENST00000680220.1 | protein_coding | 16/41 | chr14 | TogoVar | |||||||
RALGAPA1_chr14_35533356_35814295 | 35737759 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG04184.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0243 | 1 | 272 | 0.0037 | -15 | c.158 others(32): Show |
RALGAPA1 | ENSG00000174373.17 | transcript | ENST00000680220.1 | protein_coding | 12/41 | chr14 | TogoVar | |||||||
RALGAPA2_chr20_20384530_20717644 | 20567857 | TAATAAAA others(8): Show |
T | intron_variant | MODIFIER | HG02145.hp2 NA18988.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0012 | a0001c0001t0001g0015 a0001c0001t0012g0036 |
2 | 122 | 0.0164 | -15 | c.315 others(34): Show |
RALGAPA2 | ENSG00000188559.16 | transcript | ENST00000202677.12 | protein_coding | 23/39 | chr20 | TogoVar | |||||||
RALGAPA2_chr20_20384530_20717644 | 20642103 | AGAGGGGA others(8): Show |
A | intron_variant | MODIFIER | HG00741.hp2 HG02258.hp1 HG02970.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0007a0001c0001t0012 | a0001c0001t0002g0042 a0001c0001t0007g0043 a0001c0001t0012g0031 |
3 | 122 | 0.0246 | -15 | c.373 others(32): Show |
RALGAPA2 | ENSG00000188559.16 | transcript | ENST00000202677.12 | protein_coding | 5/39 | chr20 | TogoVar | |||||||
RALGPS1_chr9_126909782_127228166 | 126982922 | CTTCTTCT others(8): Show |
C | intron_variant | MODIFIER | HG02735.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0241 | 1 | 276 | 0.0036 | -15 | c.216 others(32): Show |
RALGPS1 | ENSG00000136828.19 | transcript | ENST00000259351.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
RALGPS1_chr9_126909782_127228166 | 127001086 | TACAAAAC others(8): Show |
T | intron_variant | MODIFIER | HG01069.hp1 HG01496.hp1 HG02257.hp1 others(21): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(3): Show | a0001c0001t0001g0232 a0001c0001t0001g0252 a0001c0001t0003g0105 others(21): Show |
24 | 276 | 0.0870 | -15 | c.216 others(34): Show |
RALGPS1 | ENSG00000136828.19 | transcript | ENST00000259351.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
RALGPS2_chr1_178720244_178926840 | 178788841 | CTTTCTTT others(8): Show |
C | intron_variant | MODIFIER | HG02055.hp2 HG02258.hp2 HG02486.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0009a0001c0001t0019a0001c0001t0041 | a0001c0001t0009g0138 a0001c0001t0009g0140 a0001c0001t0009g0141 others(5): Show |
8 | 306 | 0.0261 | -15 | c.213 others(32): Show |
RALGPS2 | ENSG00000116191.19 | transcript | ENST00000367635.8 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RALYL_chr8_84178274_84926844 | 84223079 | CTGCCTTT others(8): Show |
C | intron_variant | MODIFIER | HG00140.hp2 HG00741.hp1 HG03041.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0067 a0001c0001t0001g0073 a0001c0001t0001g0077 others(1): Show |
4 | 82 | 0.0488 | -15 | c.-24 others(34): Show |
RALYL | ENSG00000184672.12 | transcript | ENST00000521268.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
RALYL_chr8_84178274_84926844 | 84223081 | GCCTTTCC others(8): Show |
G | intron_variant | MODIFIER | HG01167.hp2 HG02280.hp2 HG03486.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0001g0055 others(4): Show |
7 | 82 | 0.0854 | -15 | c.-24 others(34): Show |
RALYL | ENSG00000184672.12 | transcript | ENST00000521268.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
RALYL_chr8_84178274_84926844 | 84223209 | CTCCCTTC others(8): Show |
C | intron_variant | MODIFIER | HG00140.hp2 HG00741.hp1 HG01071.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0056 others(11): Show |
14 | 82 | 0.1707 | -15 | c.-24 others(34): Show |
RALYL | ENSG00000184672.12 | transcript | ENST00000521268.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
RALYL_chr8_84178274_84926844 | 84311053 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG02895.hp2 HG03471.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 a0001c0001t0001g0007 |
2 | 82 | 0.0244 | -15 | c.-24 others(36): Show |
RALYL | ENSG00000184672.12 | transcript | ENST00000521268.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
RALYL_chr8_84178274_84926844 | 84367318 | ATTTTTTT others(8): Show |
A | intron_variant | MODIFIER | HG00140.hp1 HG01081.hp2 HG02970.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0081 a0001c0001t0002g0057 a0001c0001t0003g0065 others(2): Show |
5 | 82 | 0.0610 | -15 | c.-23 others(36): Show |
RALYL | ENSG00000184672.12 | transcript | ENST00000521268.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
RALYL_chr8_84178274_84926844 | 84501806 | CTATATTA others(8): Show |
C | intron_variant | MODIFIER | HG02896.hp1 HG02897.hp2 HG03130.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0006 | a0001c0001t0002g0052 a0001c0001t0006g0009 a0001c0001t0006g0010 |
3 | 82 | 0.0366 | -15 | c.-23 others(34): Show |
RALYL | ENSG00000184672.12 | transcript | ENST00000521268.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
RALYL_chr8_84178274_84926844 | 84907310 | TCACACAC others(8): Show |
T | intron_variant | MODIFIER | HG03471.hp1 HG06807.hp2 NA19240.hp1 |
a0001 | a0001c0001 | a0001c0001t0010a0001c0001t0016a0001c0001t0017 | a0001c0001t0010g0008 a0001c0001t0016g0002 a0001c0001t0017g0027 |
3 | 82 | 0.0366 | -15 | c.859 others(34): Show |
RALYL | ENSG00000184672.12 | transcript | ENST00000521268.6 | protein_coding | 8/8 | chr8 | TogoVar | |||||||
RALY_chr20_33988911_34089884 | 34035152 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG02486.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0244 | 1 | 290 | 0.0035 | -15 | c.-10 others(32): Show |
RALY | ENSG00000125970.12 | transcript | ENST00000246194.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
RAMP1_chr2_237854623_237917106 | 237916835 | ACCAGGTT others(8): Show |
A | downstream_gene_variant | MODIFIER | HG00642.hp2 HG01081.hp2 HG01243.hp1 others(21): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0127 a0001c0001t0001g0135 a0001c0001t0001g0136 others(21): Show |
24 | 404 | 0.0594 | -15 | c.*50 others(26): Show |
RAMP1 | ENSG00000132329.11 | transcript | ENST00000254661.5 | protein_coding | 4730 | chr2 | TogoVar | |||||||
RAMP3_chr7_45152791_45189250 | 45160330 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG01433.hp2 HG04228.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0035 | 2 | 420 | 0.0048 | -15 | c.58+ others(30): Show |
RAMP3 | ENSG00000122679.8 | transcript | ENST00000242249.8 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
RANBP17_chr5_170857018_171305015 | 170871296 | CTCTGCCT others(8): Show |
C | intron_variant | MODIFIER | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(81): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(81): Show |
84 | 192 | 0.4375 | -15 | c.19- others(30): Show |
RANBP17 | ENSG00000204764.14 | transcript | ENST00000523189.6 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
RANBP17_chr5_170857018_171305015 | 171258115 | AAATACAC others(8): Show |
A | intron_variant | MODIFIER | HG02559.hp2 HG03195.hp1 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0002 a0001c0002t0002g0003 |
2 | 192 | 0.0104 | -15 | c.277 others(34): Show |
RANBP17 | ENSG00000204764.14 | transcript | ENST00000523189.6 | protein_coding | 24/27 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
RANBP17_chr5_170857018_171305015 | 171271075 | CTTTTTTT others(8): Show |
C | intron_variant | MODIFIER | HG02622.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0163 | 1 | 192 | 0.0052 | -15 | c.294 others(34): Show |
RANBP17 | ENSG00000204764.14 | transcript | ENST00000523189.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
RANBP17_chr5_170857018_171305015 | 171282454 | ATGTTGTT others(8): Show |
A | intron_variant | MODIFIER | HG01071.hp1 HG03579.hp2 |
a0001a0009 | a0001c0001a0009c0012 | a0001c0001t0001a0009c0012t0001 | a0001c0001t0001g0140 a0009c0012t0001g0105 |
2 | 192 | 0.0104 | -15 | c.294 others(36): Show |
RANBP17 | ENSG00000204764.14 | transcript | ENST00000523189.6 | protein_coding | 25/27 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
RANBP2_chr2_108714482_108790809 | 108750556 | CCTTTTCT others(8): Show |
C | intron_variant | MODIFIER | HG01261.hp2 HG02258.hp1 HG02486.hp2 others(29): Show |
a0001a0002a0004others(7): Show | a0001c0003a0002c0010a0004c0008others(7): Show | a0001c0003t0002a0001c0003t0007a0002c0010t0012others(10): Show | a0001c0003t0002g0002 a0001c0003t0002g0065 a0001c0003t0002g0075 others(28): Show |
32 | 232 | 0.1379 | -15 | c.127 others(32): Show |
RANBP2 | ENSG00000153201.17 | transcript | ENST00000283195.11 | protein_coding | 9/28 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
RANBP3L_chr5_36241913_36306902 | 36285793 | TTGAGATT others(8): Show |
T | intron_variant | MODIFIER | HG01891.hp1 HG03041.hp1 NA21309.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0005a0002c0002t0007 | a0001c0001t0005g0114 a0001c0001t0005g0115 a0002c0002t0007g0113 |
3 | 378 | 0.0079 | -15 | c.92- others(32): Show |
RANBP3L | ENSG00000164188.9 | transcript | ENST00000296604.8 | protein_coding | 1/13 | chr5 | TogoVar | |||||||
RANBP9_chr6_13616498_13716835 | 13666600 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG01496.hp2 HG02055.hp1 |
a0001 | a0001c0002 | a0001c0002t0006 | a0001c0002t0006g0358 a0001c0002t0006g0359 |
2 | 360 | 0.0056 | -15 | c.684 others(32): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | TogoVar | |||||||
RANBP9_chr6_13616498_13716835 | 13682404 | AAAAAAAA others(8): Show |
A | intron_variant | MODIFIER | HG02055.hp2 NA19043.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | 360 | 0.0056 | -15 | c.683 others(34): Show |
RANBP9 | ENSG00000010017.13 | transcript | ENST00000011619.6 | protein_coding | 2/13 | chr6 | TogoVar | |||||||
RAP1A_chr1_111614789_111721691 | 111680798 | TAGAAGGA others(8): Show |
T | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(199): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(15): Show | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0040 others(188): Show |
202 | 380 | 0.5316 | -15 | c.-27 others(34): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
RAP1A_chr1_111614789_111721691 | 111708490 | AAAACTAA others(8): Show |
A | intron_variant | MODIFIER | HG01433.hp2 | a0002 | a0002c0002 | a0002c0002t0006 | a0002c0002t0006g0215 | 1 | 380 | 0.0026 | -15 | c.469 others(30): Show |
RAP1A | ENSG00000116473.15 | transcript | ENST00000369709.4 | protein_coding | 6/7 | chr1 | TogoVar | |||||||
RAP1B_chr12_68605899_68676901 | 68618698 | CTGTCCTA others(8): Show |
C | intron_variant | MODIFIER | HG01516.hp2 HG01517.hp2 NA20805.hp1 |
a0001 | a0001c0001 | a0001c0001t0026a0001c0001t0048 | a0001c0001t0026g0013 a0001c0001t0048g0358 |
3 | 388 | 0.0077 | -15 | c.-27 others(32): Show |
RAP1B | ENSG00000127314.18 | transcript | ENST00000250559.14 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
RAP1GAP2_chr17_2791438_3042741 | 2801593 | GGGTATGT others(8): Show |
G | intron_variant | MODIFIER | HG02056.hp1 | a0001 | a0001c0005 | a0001c0005t0120 | a0001c0005t0120g0147 | 1 | 218 | 0.0046 | -15 | c.80+ others(30): Show |
RAP1GAP2 | ENSG00000132359.17 | transcript | ENST00000254695.13 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RAP1GAP2_chr17_2791438_3042741 | 2830016 | GTGAGAAC others(8): Show |
G | intron_variant | MODIFIER | NA18945.hp2 | a0001 | a0001c0002 | a0001c0002t0010 | a0001c0002t0010g0149 | 1 | 218 | 0.0046 | -15 | c.80+ others(32): Show |
RAP1GAP2 | ENSG00000132359.17 | transcript | ENST00000254695.13 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
RAP1GAP2_chr17_2791438_3042741 | 2950559 | CACCTCAT others(8): Show |
C | intron_variant | MODIFIER | HG03654.hp2 | a0002 | a0002c0003 | a0002c0003t0006 | a0002c0003t0006g0099 | 1 | 218 | 0.0046 | -15 | c.166 others(32): Show |
RAP1GAP2 | ENSG00000132359.17 | transcript | ENST00000254695.13 | protein_coding | 3/24 | chr17 | TogoVar | |||||||
RAP1GAP_chr1_21591221_21674357 | 21616134 | CCAACACA others(8): Show |
C | intron_variant | MODIFIER | NA19070.hp1 | a0002 | a0002c0001 | a0002c0001t0001 | a0002c0001t0001g0257 | 1 | 372 | 0.0027 | -15 | c.291 others(32): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 7/24 | chr1 | TogoVar | |||||||
RAP1GAP_chr1_21591221_21674357 | 21628400 | TAAAAAAA others(8): Show |
T | intron_variant | MODIFIER | HG01261.hp2 HG02897.hp2 HG03704.hp2 |
a0002 | a0002c0001a0002c0016 | a0002c0001t0001a0002c0016t0001 | a0002c0001t0001g0094 a0002c0001t0001g0169 a0002c0016t0001g0128 |
3 | 372 | 0.0081 | -15 | c.-11 others(34): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | TogoVar | |||||||
RAP1GAP_chr1_21591221_21674357 | 21643561 | AAAAAAAA others(8): Show |
A | intron_variant | MODIFIER | HG03195.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0156 | 1 | 372 | 0.0027 | -15 | c.-11 others(34): Show |
RAP1GAP | ENSG00000076864.21 | transcript | ENST00000374765.9 | protein_coding | 2/24 | chr1 | TogoVar | |||||||
RAPGEF1_chr9_131571775_131745076 | 131627213 | CAAAAAAA others(8): Show |
C | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(92): Show |
a0001a0004a0005 | a0001c0001a0001c0002a0001c0005others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0207 others(91): Show |
95 | 368 | 0.2582 | -15 | c.120 others(32): Show |
RAPGEF1 | ENSG00000107263.19 | transcript | ENST00000683357.1 | protein_coding | 9/26 | chr9 | TogoVar | |||||||
RAPGEF1_chr9_131571775_131745076 | 131649200 | ATTTTTTT others(8): Show |
A | intron_variant | MODIFIER | HG03139.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0195 | 1 | 368 | 0.0027 | -15 | c.315 others(30): Show |
RAPGEF1 | ENSG00000107263.19 | transcript | ENST00000683357.1 | protein_coding | 3/26 | chr9 | TogoVar | |||||||
RAPGEF2_chr4_159098079_159365173 | 159182386 | CTTTTTTT others(8): Show |
C | intron_variant | MODIFIER | NA19043.hp2 NA21309.hp2 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0092 a0001c0001t0005g0093 |
2 | 194 | 0.0103 | -15 | c.70- others(30): Show |
RAPGEF2 | ENSG00000109756.10 | transcript | ENST00000691494.1 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr4 | TogoVar |