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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
C1orf56_chr1_151042751_151056420 | 151051393 | G | GA | intragenic_variant | MODIFIER | HG00438.hp2 HG01069.hp1 HG01069.hp2 others(52): Show |
a0001a0002 | a0001c0001a0001c0004a0001c0005others(1): Show | a0001c0001t0002a0001c0001t0012a0001c0001t0020others(3): Show | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(6): Show | 55 | 342 | 0.1608 | 1 | n.151 others(10): Show |
C1orf56 | ENSG00000143443.10 | gene_variant | ENSG00000143443.10 | chr1 | TogoVar | ||||||||
C1orf56_chr1_151042751_151056420 | 151051393 | G | GAA | intragenic_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(33): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0006 | a0001c0001t0005a0001c0001t0013a0001c0001t0018others(2): Show | a0001c0001t0005g0001a0001c0001t0005g0002a0001c0001t0005g0003others(9): Show | 36 | 342 | 0.1053 | 2 | n.151 others(21): Show |
C1orf56 | ENSG00000143443.10 | gene_variant | ENSG00000143443.10 | chr1 | TogoVar | ||||||||
C1orf56_chr1_151042751_151056420 | 151051393 | G | GAAA | intragenic_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(134): Show |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0001a0001c0001t0010a0001c0001t0011others(3): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(9): Show | 137 | 342 | 0.4006 | 3 | n.151 others(22): Show |
C1orf56 | ENSG00000143443.10 | gene_variant | ENSG00000143443.10 | chr1 | TogoVar | ||||||||
C1orf56_chr1_151042751_151056420 | 151051393 | G | GAAAA | intragenic_variant | MODIFIER | HG00544.hp2 HG00673.hp2 HG00733.hp1 others(42): Show |
a0001a0005 | a0001c0001a0005c0007 | a0001c0001t0003a0001c0001t0015a0001c0001t0016others(3): Show | a0001c0001t0003g0001a0001c0001t0003g0004a0001c0001t0003g0005others(7): Show | 45 | 342 | 0.1316 | 4 | n.151 others(23): Show |
C1orf56 | ENSG00000143443.10 | gene_variant | ENSG00000143443.10 | chr1 | TogoVar | ||||||||
C1orf56_chr1_151042751_151056420 | 151051393 | G | GAAAAA | intragenic_variant | MODIFIER | HG01074.hp1 HG02004.hp1 HG02683.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0007a0001c0001t0017a0001c0001t0022 | a0001c0001t0007g0001a0001c0001t0007g0005a0001c0001t0017g0001others(1): Show | 8 | 342 | 0.0234 | 5 | n.151 others(24): Show |
C1orf56 | ENSG00000143443.10 | gene_variant | ENSG00000143443.10 | chr1 | TogoVar | ||||||||
CASTOR2_chr7_74959705_75036528 | 75031517 | G | GA | intragenic_variant | MODIFIER | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(25): Show |
a0001 | a0001c0001 | a0001c0001t0011a0001c0001t0012a0001c0001t0022others(13): Show | a0001c0001t0011g0001a0001c0001t0011g0078a0001c0001t0011g0120others(25): Show | 28 | 228 | 0.1228 | 1 | n.750 others(9): Show |
CASTOR2 | ENSG00000274070.2 | gene_variant | ENSG00000274070.2 | chr7 | TogoVar | ||||||||
CCDC66_chr3_56552175_56626837 | 56621818 | T | TA | intragenic_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(116): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0003a0001c0008others(9): Show | a0001c0001t0002a0001c0001t0009a0001c0003t0002others(10): Show | a0001c0001t0002g0122a0001c0001t0002g0128a0001c0001t0002g0134others(99): Show | 119 | 372 | 0.3199 | 1 | n.566 others(9): Show |
CCDC66 | ENSG00000180376.17 | gene_variant | ENSG00000180376.17 | chr3 | TogoVar | ||||||||
CCDC66_chr3_56552175_56626837 | 56621818 | T | TAA | intragenic_variant | MODIFIER | HG00408.hp1 HG00597.hp1 HG01952.hp2 others(53): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0005a0001c0008others(11): Show | a0001c0001t0003a0001c0005t0003a0001c0008t0003others(12): Show | a0001c0001t0003g0130a0001c0001t0003g0177a0001c0005t0003g0021others(51): Show | 56 | 372 | 0.1505 | 2 | n.566 others(19): Show |
CCDC66 | ENSG00000180376.17 | gene_variant | ENSG00000180376.17 | chr3 | TogoVar | ||||||||
CCDC66_chr3_56552175_56626837 | 56621818 | T | TAAA | intragenic_variant | MODIFIER | HG01167.hp2 HG01169.hp2 HG02109.hp2 others(11): Show |
a0002a0004 | a0002c0002a0004c0007a0004c0011others(1): Show | a0002c0002t0005a0004c0007t0005a0004c0011t0005others(1): Show | a0002c0002t0005g0270a0002c0002t0005g0275a0002c0002t0005g0277others(9): Show | 14 | 372 | 0.0376 | 3 | n.566 others(20): Show |
CCDC66 | ENSG00000180376.17 | gene_variant | ENSG00000180376.17 | chr3 | TogoVar | ||||||||
CCNK_chr14_99476409_99517440 | 99512428 | G | GA | intragenic_variant | MODIFIER | HG01978.hp1 HG02055.hp1 HG02622.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0001a0001c0001t0003g0035a0001c0001t0003g0074others(3): Show | 9 | 326 | 0.0276 | 1 | n.995 others(9): Show |
CCNK | ENSG00000090061.17 | gene_variant | ENSG00000090061.17 | chr14 | TogoVar | ||||||||
CLPSL1_chr6_35776019_35793150 | 35786783 | A | AAACCTTT others(12211): Show |
intragenic_variant | MODIFIER | NA18994.hp1 | a0002 | a0002c0004 | a0002c0004t0001 | a0002c0004t0001g0083 | 1 | 444 | 0.0023 | 12218 | n.357 others(12235): Show |
CLPSL1 | ENSG00000204140.10 | gene_variant | ENSG00000204140.10 | chr6 | TogoVar | ||||||||
CLPSL1_chr6_35776019_35793150 | 35786783 | A | AAACCTTT others(12209): Show |
intragenic_variant | MODIFIER | NA18965.hp1 | a0002 | a0002c0004 | a0002c0004t0001 | a0002c0004t0001g0084 | 1 | 444 | 0.0023 | 12216 | n.357 others(12233): Show |
CLPSL1 | ENSG00000204140.10 | gene_variant | ENSG00000204140.10 | chr6 | TogoVar | ||||||||
CLPSL1_chr6_35776019_35793150 | 35786783 | A | AAACCTTT others(12210): Show |
intragenic_variant | MODIFIER | HG01243.hp2 HG03579.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0107a0001c0001t0001g0160 | 2 | 444 | 0.0045 | 12217 | n.357 others(12234): Show |
CLPSL1 | ENSG00000204140.10 | gene_variant | ENSG00000204140.10 | chr6 | TogoVar | ||||||||
CLPSL1_chr6_35776019_35793150 | 35786783 | A | AAACCTTT others(12228): Show |
intragenic_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0112 | 1 | 444 | 0.0023 | 12235 | n.357 others(12252): Show |
CLPSL1 | ENSG00000204140.10 | gene_variant | ENSG00000204140.10 | chr6 | TogoVar | ||||||||
CLPSL1_chr6_35776019_35793150 | 35786783 | A | AAACCTTT others(12211): Show |
intragenic_variant | MODIFIER | NA19055.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0050 | 1 | 444 | 0.0023 | 12218 | n.357 others(12235): Show |
CLPSL1 | ENSG00000204140.10 | gene_variant | ENSG00000204140.10 | chr6 | TogoVar | ||||||||
CLPSL1_chr6_35776019_35793150 | 35786783 | A | AAACCTTT others(12230): Show |
intragenic_variant | MODIFIER | HG02717.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0109 | 1 | 444 | 0.0023 | 12237 | n.357 others(12254): Show |
CLPSL1 | ENSG00000204140.10 | gene_variant | ENSG00000204140.10 | chr6 | TogoVar | ||||||||
CLPSL1_chr6_35776019_35793150 | 35786783 | A | AAACCTTT others(12228): Show |
intragenic_variant | MODIFIER | NA19240.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0110 | 1 | 444 | 0.0023 | 12235 | n.357 others(12252): Show |
CLPSL1 | ENSG00000204140.10 | gene_variant | ENSG00000204140.10 | chr6 | TogoVar | ||||||||
CLPSL1_chr6_35776019_35793150 | 35786783 | A | AAACCTTT others(12226): Show |
intragenic_variant | MODIFIER | NA19043.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0108 | 1 | 444 | 0.0023 | 12233 | n.357 others(12250): Show |
CLPSL1 | ENSG00000204140.10 | gene_variant | ENSG00000204140.10 | chr6 | TogoVar | ||||||||
CLPSL1_chr6_35776019_35793150 | 35786783 | A | AAACCTTT others(12211): Show |
intragenic_variant | MODIFIER | NA18964.hp2 NA18982.hp1 |
a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0038 | 2 | 444 | 0.0045 | 12218 | n.357 others(12235): Show |
CLPSL1 | ENSG00000204140.10 | gene_variant | ENSG00000204140.10 | chr6 | TogoVar | ||||||||
CLPSL1_chr6_35776019_35793150 | 35786783 | A | AAACCTTT others(12225): Show |
intragenic_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0125 | 1 | 444 | 0.0023 | 12232 | n.357 others(12249): Show |
CLPSL1 | ENSG00000204140.10 | gene_variant | ENSG00000204140.10 | chr6 | TogoVar | ||||||||
CLPSL1_chr6_35776019_35793150 | 35786783 | A | AAACCTTT others(12223): Show |
intragenic_variant | MODIFIER | HG02970.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0126 | 1 | 444 | 0.0023 | 12230 | n.357 others(12247): Show |
CLPSL1 | ENSG00000204140.10 | gene_variant | ENSG00000204140.10 | chr6 | TogoVar | ||||||||
CLPSL1_chr6_35776019_35793150 | 35786783 | A | AAACCTTT others(12219): Show |
intragenic_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0129 | 1 | 444 | 0.0023 | 12226 | n.357 others(12243): Show |
CLPSL1 | ENSG00000204140.10 | gene_variant | ENSG00000204140.10 | chr6 | TogoVar | ||||||||
CLPSL1_chr6_35776019_35793150 | 35786783 | A | AAACCTTT others(12218): Show |
intragenic_variant | MODIFIER | HG02109.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0127 | 1 | 444 | 0.0023 | 12225 | n.357 others(12242): Show |
CLPSL1 | ENSG00000204140.10 | gene_variant | ENSG00000204140.10 | chr6 | TogoVar | ||||||||
CLPSL1_chr6_35776019_35793150 | 35786783 | A | AAACCTTT others(12222): Show |
intragenic_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0121 | 1 | 444 | 0.0023 | 12229 | n.357 others(12246): Show |
CLPSL1 | ENSG00000204140.10 | gene_variant | ENSG00000204140.10 | chr6 | TogoVar | ||||||||
CLPSL1_chr6_35776019_35793150 | 35786783 | A | AAACCTTT others(12213): Show |
intragenic_variant | MODIFIER | NA19006.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0057 | 1 | 444 | 0.0023 | 12220 | n.357 others(12237): Show |
CLPSL1 | ENSG00000204140.10 | gene_variant | ENSG00000204140.10 | chr6 | TogoVar | ||||||||
CLPSL1_chr6_35776019_35793150 | 35786783 | A | AAACCTTT others(12211): Show |
intragenic_variant | MODIFIER | HG00558.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0060 | 1 | 444 | 0.0023 | 12218 | n.357 others(12235): Show |
CLPSL1 | ENSG00000204140.10 | gene_variant | ENSG00000204140.10 | chr6 | TogoVar | ||||||||
CLPSL1_chr6_35776019_35793150 | 35786783 | A | AAACCTTT others(12210): Show |
intragenic_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0155 | 1 | 444 | 0.0023 | 12217 | n.357 others(12234): Show |
CLPSL1 | ENSG00000204140.10 | gene_variant | ENSG00000204140.10 | chr6 | TogoVar | ||||||||
CLPSL1_chr6_35776019_35793150 | 35786965 | T | TGGAGCCT others(12227): Show |
intragenic_variant | MODIFIER | HG02109.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0124 | 1 | 444 | 0.0023 | 12234 | n.357 others(12251): Show |
CLPSL1 | ENSG00000204140.10 | gene_variant | ENSG00000204140.10 | chr6 | TogoVar | ||||||||
CMC1_chr3_28236619_28330142 | 28325125 | T | TA | intragenic_variant | MODIFIER | HG00558.hp1 HG00597.hp1 HG00597.hp2 others(66): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0005a0001c0001t0010others(3): Show | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0007others(57): Show | 69 | 338 | 0.2041 | 1 | n.283 others(9): Show |
CMC1 | ENSG00000187118.14 | gene_variant | ENSG00000187118.14 | chr3 | TogoVar | ||||||||
COX7B_chrX_77894468_77912376 | 77906317 | A | AGTGTCAC others(3327): Show |
intragenic_variant | MODIFIER | HG02040.hp1 | a0001 | a0001c0001 | a0001c0001t0022 | a0001c0001t0022g0002 | 1 | 294 | 0.0034 | 3334 | n.779 others(3351): Show |
COX7B | ENSG00000131174.7 | gene_variant | ENSG00000131174.7 | chrX | TogoVar | ||||||||
DLEC1_chr3_38034208_38129025 | 38124010 | C | CA | intragenic_variant | MODIFIER | HG01884.hp1 HG02280.hp2 HG02630.hp1 others(7): Show |
a0001a0002 | a0001c0003a0001c0014a0001c0029others(1): Show | a0001c0003t0004a0001c0014t0005a0001c0029t0005others(1): Show | a0001c0003t0004g0011a0001c0003t0004g0164a0001c0003t0004g0165others(6): Show | 10 | 298 | 0.0336 | 1 | n.381 others(9): Show |
DLEC1 | ENSG00000008226.20 | gene_variant | ENSG00000008226.20 | chr3 | TogoVar | ||||||||
EBLN2_chr3_73056659_73068337 | 73063318 | T | TA | intragenic_variant | MODIFIER | HG01261.hp1 HG02129.hp1 HG02280.hp1 others(16): Show |
a0001a0002a0004 | a0001c0001a0001c0004a0001c0013others(2): Show | a0001c0001t0004a0001c0001t0021a0001c0004t0004others(4): Show | a0001c0001t0004g0000a0001c0001t0021g0000a0001c0004t0004g0000others(4): Show | 19 | 428 | 0.0444 | 1 | n.730 others(9): Show |
EBLN2 | ENSG00000255423.1 | gene_variant | ENSG00000255423.1 | chr3 | TogoVar | ||||||||
EBLN2_chr3_73056659_73068337 | 73063318 | T | TAA | intragenic_variant | MODIFIER | HG02109.hp1 HG02559.hp1 HG02630.hp1 others(6): Show |
a0001 | a0001c0004 | a0001c0004t0007a0001c0004t0016 | a0001c0004t0007g0000a0001c0004t0016g0000 | 9 | 428 | 0.0210 | 2 | n.730 others(19): Show |
EBLN2 | ENSG00000255423.1 | gene_variant | ENSG00000255423.1 | chr3 | TogoVar | ||||||||
EBLN2_chr3_73056659_73068337 | 73063318 | TA | T | intragenic_variant | MODIFIER | HG00733.hp1 HG00733.hp2 HG01361.hp1 others(7): Show |
a0001a0004 | a0001c0001a0004c0005 | a0001c0001t0006a0004c0005t0006 | a0001c0001t0006g0000a0004c0005t0006g0000 | 10 | 428 | 0.0234 | -1 | n.730 others(9): Show |
EBLN2 | ENSG00000255423.1 | gene_variant | ENSG00000255423.1 | chr3 | TogoVar | ||||||||
ESCO2_chr8_27769554_27810316 | 27805287 | C | CA | intragenic_variant | MODIFIER | HG00408.hp2 HG01517.hp1 HG01884.hp1 others(23): Show |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0008a0001c0001t0015a0001c0001t0030others(2): Show | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0043others(21): Show | 26 | 380 | 0.0684 | 1 | n.278 others(9): Show |
ESCO2 | ENSG00000171320.15 | gene_variant | ENSG00000171320.15 | chr8 | TogoVar | ||||||||
ESCO2_chr8_27769554_27810316 | 27805287 | C | CAA | intragenic_variant | MODIFIER | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(36): Show |
a0001a0006 | a0001c0001a0006c0005 | a0001c0001t0002a0001c0001t0043a0006c0005t0002 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0012others(26): Show | 39 | 380 | 0.1026 | 2 | n.278 others(19): Show |
ESCO2 | ENSG00000171320.15 | gene_variant | ENSG00000171320.15 | chr8 | TogoVar | ||||||||
ESCO2_chr8_27769554_27810316 | 27805287 | C | CAAA | intragenic_variant | MODIFIER | HG00673.hp1 HG01099.hp2 HG01123.hp1 others(28): Show |
a0001a0003a0006 | a0001c0001a0003c0003a0006c0005 | a0001c0001t0006a0001c0001t0041a0001c0001t0044others(4): Show | a0001c0001t0006g0005a0001c0001t0006g0011a0001c0001t0006g0012others(26): Show | 31 | 380 | 0.0816 | 3 | n.278 others(20): Show |
ESCO2 | ENSG00000171320.15 | gene_variant | ENSG00000171320.15 | chr8 | TogoVar | ||||||||
ESCO2_chr8_27769554_27810316 | 27805287 | C | CAAAA | intragenic_variant | MODIFIER | HG01952.hp2 HG01993.hp1 HG04184.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0011a0001c0001t0042 | a0001c0001t0011g0002a0001c0001t0011g0013a0001c0001t0011g0022others(7): Show | 12 | 380 | 0.0316 | 4 | n.278 others(21): Show |
ESCO2 | ENSG00000171320.15 | gene_variant | ENSG00000171320.15 | chr8 | TogoVar | ||||||||
ESCO2_chr8_27769554_27810316 | 27805287 | C | CAAAAA | intragenic_variant | MODIFIER | HG01358.hp2 HG02886.hp2 HG03239.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0013a0001c0001t0045 | a0001c0001t0013g0002a0001c0001t0013g0013a0001c0001t0013g0022others(5): Show | 8 | 380 | 0.0211 | 5 | n.278 others(22): Show |
ESCO2 | ENSG00000171320.15 | gene_variant | ENSG00000171320.15 | chr8 | TogoVar | ||||||||
ESCO2_chr8_27769554_27810316 | 27805287 | C | CAAAAAAA others(4): Show |
intragenic_variant | MODIFIER | HG02630.hp2 | a0001 | a0001c0001 | a0001c0001t0047 | a0001c0001t0047g0104 | 1 | 380 | 0.0026 | 11 | n.278 others(28): Show |
ESCO2 | ENSG00000171320.15 | gene_variant | ENSG00000171320.15 | chr8 | TogoVar | ||||||||
ESCO2_chr8_27769554_27810316 | 27805287 | C | CAAAAAAA others(19): Show |
intragenic_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0001 | a0001c0001t0040 | a0001c0001t0040g0174 | 1 | 380 | 0.0026 | 26 | n.278 others(43): Show |
ESCO2 | ENSG00000171320.15 | gene_variant | ENSG00000171320.15 | chr8 | TogoVar | ||||||||
FSTL3_chr19_671392_688385 | 683383 | C | CAAAG | intragenic_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(295): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(34): Show | a0001c0001t0002g0008a0001c0001t0002g0018a0001c0001t0002g0089others(124): Show | 298 | 434 | 0.6866 | 4 | n.683 others(17): Show |
FSTL3 | ENSG00000070404.10 | gene_variant | ENSG00000070404.10 | chr19 | TogoVar | ||||||||
GLS_chr2_190875821_190970552 | 190965542 | C | CA | intragenic_variant | MODIFIER | HG00738.hp2 HG02280.hp1 HG02280.hp2 others(6): Show |
a0001a0006 | a0001c0001a0001c0004a0001c0008others(1): Show | a0001c0001t0039a0001c0001t0053a0001c0001t0058others(3): Show | a0001c0001t0039g0180a0001c0001t0053g0332a0001c0001t0058g0311others(6): Show | 9 | 380 | 0.0237 | 1 | n.190 others(10): Show |
GLS | ENSG00000115419.14 | gene_variant | ENSG00000115419.14 | chr2 | TogoVar | ||||||||
GPR21_chr9_123028667_123040665 | 123035639 | CGT | C | intragenic_variant | MODIFIER | HG02257.hp1 HG02976.hp1 HG03834.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0001 | 4 | 358 | 0.0112 | -2 | n.123 others(21): Show |
GPR21 | ENSG00000188394.8 | gene_variant | ENSG00000188394.8 | chr9 | TogoVar | ||||||||
GPR21_chr9_123028667_123040665 | 123035639 | CGTGT | C | intragenic_variant | MODIFIER | HG02109.hp1 HG02165.hp1 HG02970.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0001 | 5 | 358 | 0.0140 | -4 | n.123 others(23): Show |
GPR21 | ENSG00000188394.8 | gene_variant | ENSG00000188394.8 | chr9 | TogoVar | ||||||||
GPR21_chr9_123028667_123040665 | 123035639 | CGTGTGT | C | intragenic_variant | MODIFIER | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(27): Show |
a0001a0004 | a0001c0001a0004c0003 | a0001c0001t0005a0004c0003t0005 | a0001c0001t0005g0001a0001c0001t0005g0003a0004c0003t0005g0001 | 30 | 358 | 0.0838 | -6 | n.123 others(25): Show |
GPR21 | ENSG00000188394.8 | gene_variant | ENSG00000188394.8 | chr9 | TogoVar | ||||||||
GPR21_chr9_123028667_123040665 | 123035639 | CGTGTGTG others(1): Show |
C | intragenic_variant | MODIFIER | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(59): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0008 | a0001c0001t0003a0001c0001t0009a0002c0002t0003others(1): Show | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0009g0001others(2): Show | 62 | 358 | 0.1732 | -8 | n.123 others(27): Show |
GPR21 | ENSG00000188394.8 | gene_variant | ENSG00000188394.8 | chr9 | TogoVar | ||||||||
GPR21_chr9_123028667_123040665 | 123035639 | CGTGTGTG others(3): Show |
C | intragenic_variant | MODIFIER | HG00099.hp1 HG00438.hp1 HG00558.hp2 others(130): Show |
a0001 | a0001c0001a0001c0004a0001c0007 | a0001c0001t0001a0001c0001t0011a0001c0001t0014others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0011g0001others(3): Show | 133 | 358 | 0.3715 | -10 | n.123 others(29): Show |
GPR21 | ENSG00000188394.8 | gene_variant | ENSG00000188394.8 | chr9 | TogoVar | ||||||||
GPR21_chr9_123028667_123040665 | 123035639 | CGTGTGTG others(5): Show |
C | intragenic_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(68): Show |
a0001a0003a0006others(1): Show | a0001c0001a0001c0006a0003c0009others(2): Show | a0001c0001t0002a0001c0006t0002a0003c0009t0002others(2): Show | a0001c0001t0002g0001a0001c0006t0002g0001a0003c0009t0002g0001others(2): Show | 71 | 358 | 0.1983 | -12 | n.123 others(31): Show |
GPR21 | ENSG00000188394.8 | gene_variant | ENSG00000188394.8 | chr9 | TogoVar | ||||||||
GPR21_chr9_123028667_123040665 | 123035639 | CGTGTGTG others(7): Show |
C | intragenic_variant | MODIFIER | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(35): Show |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0001 | 38 | 358 | 0.1062 | -14 | n.123 others(33): Show |
GPR21 | ENSG00000188394.8 | gene_variant | ENSG00000188394.8 | chr9 | TogoVar |