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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
C1orf56_chr1_151042751_151056420 | 151051393 | G | GA | intragenic_variant | MODIFIER | HG00438.hp2 HG01069.hp1 HG01069.hp2 others(52): Show |
a0001a0002 | a0001c0001a0001c0004a0001c0005others(1): Show | a0001c0001t0002a0001c0001t0012a0001c0001t0021others(3): Show | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(6): Show |
55 | 80 | 0.6875 | 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 | a0001c0001t0005g0001 a0001c0001t0005g0002 a0001c0001t0005g0003 others(9): Show |
36 | 61 | 0.5902 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(9): Show |
137 | 162 | 0.8457 | 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 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0005 others(7): Show |
45 | 70 | 0.6429 | 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 | a0001c0001t0007a0001c0001t0017a0001c0001t0023 | a0001c0001t0007g0001 a0001c0001t0007g0005 a0001c0001t0017g0001 others(1): Show |
8 | 33 | 0.2424 | 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 | a0001c0001t0011g0003 a0001c0001t0011g0084 a0001c0001t0011g0118 others(25): Show |
28 | 196 | 0.1429 | 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(2): Show | a0001c0001a0001c0003a0001c0008others(9): Show | a0001c0001t0002a0001c0001t0009a0001c0003t0002others(10): Show | a0001c0001t0002g0001 a0001c0001t0002g0030 a0001c0001t0002g0123 others(93): Show |
119 | 295 | 0.4034 | 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(5): Show | a0001c0001a0001c0005a0001c0008others(11): Show | a0001c0001t0003a0001c0005t0003a0001c0008t0003others(12): Show | a0001c0001t0003g0030 a0001c0001t0003g0144 a0001c0005t0003g0005 others(46): Show |
56 | 232 | 0.2414 | 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 | a0002c0002t0005g0038 a0002c0002t0005g0239 a0002c0002t0005g0241 others(5): Show |
14 | 190 | 0.0737 | 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 | a0001c0001t0003g0001 a0001c0001t0003g0034 a0001c0001t0003g0075 others(3): Show |
9 | 315 | 0.0286 | 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 | a0002c0004t0001g0081 | 1 | 393 | 0.0025 | 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 | a0002c0004t0001g0082 | 1 | 393 | 0.0025 | 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 | a0001c0001t0001g0105 a0001c0001t0001g0156 |
2 | 394 | 0.0051 | 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 | a0001c0001t0001g0110 | 1 | 393 | 0.0025 | 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 | a0001c0001t0001g0048 | 1 | 393 | 0.0025 | 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 | a0001c0001t0001g0107 | 1 | 393 | 0.0025 | 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 | a0001c0001t0001g0108 | 1 | 393 | 0.0025 | 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 | a0001c0001t0001g0106 | 1 | 393 | 0.0025 | 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 | a0001c0005t0001g0037 | 2 | 394 | 0.0051 | 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 | a0001c0001t0001g0123 | 1 | 393 | 0.0025 | 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 | a0001c0001t0001g0124 | 1 | 393 | 0.0025 | 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 | a0001c0001t0001g0127 | 1 | 393 | 0.0025 | 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 | a0001c0001t0001g0125 | 1 | 393 | 0.0025 | 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 | a0001c0001t0001g0119 | 1 | 393 | 0.0025 | 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 | a0001c0001t0001g0055 | 1 | 393 | 0.0025 | 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 | a0001c0001t0001g0058 | 1 | 393 | 0.0025 | 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 | a0001c0001t0001g0151 | 1 | 393 | 0.0025 | 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 | a0001c0001t0001g0122 | 1 | 442 | 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 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0003 others(55): Show |
69 | 330 | 0.2091 | 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 | a0001c0001t0020 | a0001c0001t0020g0002 | 1 | 292 | 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 | a0001c0003t0004g0011 a0001c0003t0004g0164 a0001c0003t0004g0165 others(6): Show |
10 | 295 | 0.0339 | 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 | a0001c0001t0004g0000 a0001c0001t0021g0000 a0001c0004t0004g0000 others(4): Show |
19 | 403 | 0.0471 | 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 | a0001c0004t0007g0000 a0001c0004t0016g0000 |
9 | 393 | 0.0229 | 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 | a0001c0001t0006g0000 a0004c0005t0006g0000 |
10 | 394 | 0.0254 | -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 | a0001c0001t0001a0001c0001t0005a0001c0001t0016others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(19): Show |
26 | 189 | 0.1376 | 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 |
a0001a0005 | a0001c0001a0005c0005 | a0001c0001t0001a0005c0005t0001 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(23): Show |
39 | 202 | 0.1931 | 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 |
a0001a0003a0005 | a0001c0001a0003c0003a0005c0005 | a0001c0001t0001a0001c0001t0016a0001c0001t0030others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(22): Show |
31 | 194 | 0.1598 | 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 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0028 others(6): Show |
12 | 175 | 0.0686 | 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 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0029 others(5): Show |
8 | 171 | 0.0468 | 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 | a0001c0001t0001 | a0001c0001t0001g0099 | 1 | 164 | 0.0061 | 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 | a0001c0001t0029 | a0001c0001t0029g0145 | 1 | 164 | 0.0061 | 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 |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0002c0007others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(25): Show | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0014 others(105): Show |
298 | 432 | 0.6898 | 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 |
a0001a0005 | a0001c0001a0001c0004a0001c0008others(1): Show | a0001c0001t0038a0001c0001t0052a0001c0001t0057others(3): Show | a0001c0001t0038g0180 a0001c0001t0052g0332 a0001c0001t0057g0311 others(6): Show |
9 | 374 | 0.0241 | 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 | a0001c0001t0001 | a0001c0001t0001g0001 | 4 | 11 | 0.3636 | -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 | a0001c0001t0001 | a0001c0001t0001g0001 | 5 | 12 | 0.4167 | -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 |
a0001a0006 | a0001c0001a0006c0003 | a0001c0001t0001a0006c0003t0001 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0006c0003t0001g0001 |
30 | 37 | 0.8108 | -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 |
a0001a0002a0007 | a0001c0001a0002c0002a0007c0008 | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(1): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0002g0001 others(2): Show |
62 | 69 | 0.8986 | -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(129): Show |
a0001 | a0001c0001a0001c0004a0001c0007 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(2): Show | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0003g0001 others(3): Show |
132 | 139 | 0.9496 | -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 |
a0001a0003a0004others(1): Show | a0001c0001a0001c0006a0003c0009others(2): Show | a0001c0001t0001a0001c0006t0001a0003c0009t0001others(2): Show | a0001c0001t0001g0001 a0001c0006t0001g0001 a0003c0009t0001g0001 others(2): Show |
71 | 78 | 0.9103 | -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 | a0001c0001t0001 | a0001c0001t0001g0001 | 38 | 45 | 0.8444 | -14 | n.123 others(33): Show |
GPR21 | ENSG00000188394.8 | gene_variant | ENSG00000188394.8 | chr9 | TogoVar |