view | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
LACC1_chr13_43874904_43898932 | 43882564 | G | GATATATA others(13): Show |
intron_variant | MODIFIER | HG00423.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0064 | 1 | 456 | 0.0022 | 20 | c.741 others(35): Show |
LACC1 | ENSG00000179630.11 | transcript | ENST00000325686.7 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
LACTB2_chr8_70632266_70674185 | 70668748 | G | GTTTTTTT others(13): Show |
intron_variant | MODIFIER | HG01192.hp1 HG01993.hp2 |
a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0020 | 2 | 352 | 0.0057 | 20 | c.122 others(35): Show |
LACTB2 | ENSG00000147592.9 | transcript | ENST00000276590.5 | protein_coding | 1/6 | chr8 | TogoVar | |||||||
LAD1_chr1_201375833_201404324 | 201382516 | T | TGAAATGA others(13): Show |
intron_variant | MODIFIER | HG02630.hp1 HG02818.hp1 HG02965.hp1 |
a0007a0009 | a0007c0007a0009c0010 | a0007c0007t0005a0009c0010t0005 | a0007c0007t0005g0115a0007c0007t0005g0116a0009c0010t0005g0071 | 3 | 432 | 0.0069 | 20 | c.147 others(37): Show |
LAD1 | ENSG00000159166.15 | transcript | ENST00000391967.7 | protein_coding | 8/9 | chr1 | TogoVar | |||||||
LAIR2_chr19_54497831_54515687 | 54514555 | G | GTTTTTTT others(13): Show |
downstream_gene_variant | MODIFIER | HG02647.hp1 | a0003 | a0003c0003 | a0003c0003t0004 | a0003c0003t0004g0018 | 1 | 475 | 0.0021 | 20 | c.*39 others(31): Show |
LAIR2 | ENSG00000167618.10 | transcript | ENST00000301202.7 | protein_coding | 3869 | chr19 | TogoVar | |||||||
LAMA1_chr18_6936742_7122797 | 7031680 | C | CAAATAAA others(13): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(59): Show |
a0001a0002a0003others(40): Show | a0001c0161a0001c0170a0001c0171others(54): Show | a0001c0161t0001a0001c0170t0002a0001c0171t0002others(55): Show | a0001c0161t0001g0155a0001c0170t0002g0111a0001c0171t0002g0110others(59): Show | 62 | 278 | 0.2230 | 20 | c.227 others(37): Show |
LAMA1 | ENSG00000101680.16 | transcript | ENST00000389658.4 | protein_coding | 16/62 | chr18 | TogoVar | |||||||
LAMA2_chr6_128878138_129521566 | 128962185 | T | TATATATA others(13): Show |
intron_variant | MODIFIER | HG03195.hp1 | a0002 | a0002c0003 | a0002c0003t0005 | a0002c0003t0005g0010 | 1 | 88 | 0.0114 | 20 | c.112 others(39): Show |
LAMA2 | ENSG00000196569.14 | transcript | ENST00000421865.3 | protein_coding | 1/64 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
LAMA2_chr6_128878138_129521566 | 128962185 | T | TATATATA others(13): Show |
intron_variant | MODIFIER | NA20129.hp2 | a0033 | a0033c0058 | a0033c0058t0009 | a0033c0058t0009g0004 | 1 | 88 | 0.0114 | 20 | c.112 others(39): Show |
LAMA2 | ENSG00000196569.14 | transcript | ENST00000421865.3 | protein_coding | 1/64 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
LAMA2_chr6_128878138_129521566 | 129048493 | T | TTTCTTTC others(13): Show |
intron_variant | MODIFIER | HG00099.hp2 | a0004 | a0004c0048 | a0004c0048t0003 | a0004c0048t0003g0013 | 1 | 88 | 0.0114 | 20 | c.113 others(37): Show |
LAMA2 | ENSG00000196569.14 | transcript | ENST00000421865.3 | protein_coding | 1/64 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
LAMA2_chr6_128878138_129521566 | 129048540 | C | CCTTCCTT others(13): Show |
intron_variant | MODIFIER | HG02723.hp1 | a0017 | a0017c0071 | a0017c0071t0005 | a0017c0071t0005g0050 | 1 | 88 | 0.0114 | 20 | c.113 others(37): Show |
LAMA2 | ENSG00000196569.14 | transcript | ENST00000421865.3 | protein_coding | 1/64 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
LAMA2_chr6_128878138_129521566 | 129066038 | G | GTATGTCT others(13): Show |
intron_variant | MODIFIER | HG01074.hp2 HG01261.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0056 | 2 | 88 | 0.0227 | 20 | c.396 others(37): Show |
LAMA2 | ENSG00000196569.14 | transcript | ENST00000421865.3 | protein_coding | 3/64 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
LAMA2_chr6_128878138_129521566 | 129205478 | G | GTATATAT others(13): Show |
intron_variant | MODIFIER | HG00140.hp1 HG02723.hp1 |
a0003a0017 | a0003c0027a0017c0071 | a0003c0027t0001a0017c0071t0005 | a0003c0027t0001g0002a0017c0071t0005g0050 | 2 | 88 | 0.0227 | 20 | c.178 others(41): Show |
LAMA2 | ENSG00000196569.14 | transcript | ENST00000421865.3 | protein_coding | 12/64 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
LAMA2_chr6_128878138_129521566 | 129309902 | A | ATTTTTTT others(13): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0004 | a0004c0051 | a0004c0051t0001 | a0004c0051t0001g0008 | 1 | 88 | 0.0114 | 20 | c.317 others(39): Show |
LAMA2 | ENSG00000196569.14 | transcript | ENST00000421865.3 | protein_coding | 22/64 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
LAMA2_chr6_128878138_129521566 | 129326745 | T | TATATATA others(13): Show |
intron_variant | MODIFIER | HG00140.hp1 HG03710.hp2 |
a0003 | a0003c0027a0003c0030 | a0003c0027t0001a0003c0030t0002 | a0003c0027t0001g0002a0003c0030t0002g0041 | 2 | 88 | 0.0227 | 20 | c.417 others(39): Show |
LAMA2 | ENSG00000196569.14 | transcript | ENST00000421865.3 | protein_coding | 28/64 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
LAMA2_chr6_128878138_129521566 | 129446514 | A | AGAGGGGA others(13): Show |
intron_variant | MODIFIER | HG02257.hp2 | a0034 | a0034c0055 | a0034c0055t0002 | a0034c0055t0002g0030 | 1 | 88 | 0.0114 | 20 | c.642 others(37): Show |
LAMA2 | ENSG00000196569.14 | transcript | ENST00000421865.3 | protein_coding | 45/64 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
LAMA3_chr18_23684453_23960066 | 23687746 | T | TTGTGTGT others(13): Show |
upstream_gene_variant | MODIFIER | HG02818.hp1 HG03041.hp1 HG03540.hp1 others(1): Show |
a0001 | a0001c0010a0001c0011a0001c0023 | a0001c0010t0001a0001c0011t0001a0001c0023t0001 | a0001c0010t0001g0158a0001c0011t0001g0113a0001c0011t0001g0114others(1): Show | 4 | 280 | 0.0143 | 20 | c.-19 others(31): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000313654.14 | protein_coding | 1706 | chr18 | TogoVar | |||||||
LAMA3_chr18_23684453_23960066 | 23699024 | T | TAGAGAGA others(13): Show |
intron_variant | MODIFIER | HG02257.hp1 | a0036 | a0036c0025 | a0036c0025t0001 | a0036c0025t0001g0149 | 1 | 280 | 0.0036 | 20 | c.294 others(37): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000313654.14 | protein_coding | 1/74 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
LAMA3_chr18_23684453_23960066 | 23837570 | G | GATATATA others(13): Show |
intron_variant | MODIFIER | HG00099.hp2 HG01074.hp2 HG01099.hp2 others(30): Show |
a0001a0003a0005others(4): Show | a0001c0001a0001c0010a0001c0011others(6): Show | a0001c0001t0002a0001c0010t0001a0001c0011t0001others(6): Show | a0001c0001t0002g0063a0001c0001t0002g0075a0001c0001t0002g0161others(30): Show | 33 | 280 | 0.1179 | 20 | c.309 others(37): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000313654.14 | protein_coding | 25/74 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
LAMA4_chr6_112102931_112259567 | 112130298 | T | TTGTGTGT others(13): Show |
intron_variant | MODIFIER | HG02622.hp1 | a0012 | a0012c0028 | a0012c0028t0002 | a0012c0028t0002g0155 | 1 | 314 | 0.0032 | 20 | c.396 others(37): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 29/38 | chr6 | TogoVar | |||||||
LAMA4_chr6_112102931_112259567 | 112190947 | C | CCTTTCTT others(13): Show |
intron_variant | MODIFIER | HG01175.hp1 HG01515.hp1 NA18971.hp1 |
a0003a0004a0007 | a0003c0004a0004c0007a0007c0014 | a0003c0004t0001a0004c0007t0014a0007c0014t0002 | a0003c0004t0001g0018a0004c0007t0014g0300a0007c0014t0002g0292 | 3 | 314 | 0.0096 | 20 | c.718 others(35): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | TogoVar | |||||||
LAMA4_chr6_112102931_112259567 | 112190947 | C | CTTTCCTT others(13): Show |
intron_variant | MODIFIER | NA18946.hp1 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0235 | 1 | 314 | 0.0032 | 20 | c.718 others(35): Show |
LAMA4 | ENSG00000112769.20 | transcript | ENST00000230538.12 | protein_coding | 6/38 | chr6 | TogoVar | |||||||
LAMA5_chr20_62304065_62372312 | 62309639 | T | TGGGGGGT others(13): Show |
intron_variant | MODIFIER | HG01358.hp1 HG02055.hp1 HG02717.hp2 others(2): Show |
a0049a0064a0072others(2): Show | a0049c0121a0064c0040a0072c0042others(2): Show | a0049c0121t0006a0064c0040t0001a0072c0042t0001others(2): Show | a0049c0121t0006g0076a0064c0040t0001g0023a0072c0042t0001g0021others(2): Show | 5 | 186 | 0.0269 | 20 | c.109 others(37): Show |
LAMA5 | ENSG00000130702.15 | transcript | ENST00000252999.7 | protein_coding | 79/79 | chr20 | TogoVar | |||||||
LAMA5_chr20_62304065_62372312 | 62317970 | T | TGGGGAAG others(13): Show |
intron_variant | MODIFIER | HG01256.hp1 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0132 | 1 | 186 | 0.0054 | 20 | c.724 others(37): Show |
LAMA5 | ENSG00000130702.15 | transcript | ENST00000252999.7 | protein_coding | 53/79 | chr20 | TogoVar | |||||||
LAMA5_chr20_62304065_62372312 | 62360602 | G | GTGGGTGG others(13): Show |
intron_variant | MODIFIER | HG01256.hp2 HG01358.hp2 HG02258.hp1 others(4): Show |
a0000a0001a0003others(4): Show | a0000c0065a0001c0001a0003c0002others(4): Show | a0000c0065t0001a0001c0001t0001a0003c0002t0001others(4): Show | a0000c0065t0001g0041a0001c0001t0001g0115a0003c0002t0001g0028others(4): Show | 7 | 186 | 0.0376 | 20 | c.450 others(37): Show |
LAMA5 | ENSG00000130702.15 | transcript | ENST00000252999.7 | protein_coding | 2/79 | chr20 | TogoVar | |||||||
LAMA5_chr20_62304065_62372312 | 62360614 | A | AGGAATAG others(13): Show |
intron_variant | MODIFIER | HG01243.hp2 HG01943.hp2 NA18971.hp1 |
a0006a0042 | a0006c0011a0042c0099 | a0006c0011t0001a0042c0099t0001 | a0006c0011t0001g0093a0006c0011t0001g0095a0042c0099t0001g0094 | 3 | 186 | 0.0161 | 20 | c.450 others(37): Show |
LAMA5 | ENSG00000130702.15 | transcript | ENST00000252999.7 | protein_coding | 2/79 | chr20 | TogoVar | |||||||
LAMB1_chr7_107918799_108008161 | 107977003 | C | CCTTTCCT others(13): Show |
intron_variant | MODIFIER | HG03516.hp1 | a0001 | a0001c0045 | a0001c0045t0001 | a0001c0045t0001g0038 | 1 | 364 | 0.0028 | 20 | c.100 others(39): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | TogoVar | |||||||
LAMB3_chr1_209609870_209657425 | 209624880 | G | GAGGAAGG others(13): Show |
intron_variant | MODIFIER | HG02004.hp1 HG02148.hp2 NA18990.hp1 others(1): Show |
a0001a0010 | a0001c0003a0010c0031 | a0001c0003t0002a0010c0031t0002a0010c0031t0006 | a0001c0003t0002g0044a0010c0031t0002g0299a0010c0031t0006g0300 | 4 | 444 | 0.0090 | 20 | c.197 others(37): Show |
LAMB3 | ENSG00000196878.15 | transcript | ENST00000356082.9 | protein_coding | 14/22 | chr1 | TogoVar | |||||||
LAMB4_chr7_108018553_108135361 | 108024714 | G | GATCCATC others(13): Show |
intron_variant | MODIFIER | HG02970.hp2 | a0007 | a0007c0011 | a0007c0011t0002 | a0007c0011t0002g0102 | 1 | 292 | 0.0034 | 20 | c.514 others(37): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | TogoVar | |||||||
LAMB4_chr7_108018553_108135361 | 108024739 | A | ATCCATCC others(13): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0016 | a0016c0061 | a0016c0061t0002 | a0016c0061t0002g0155 | 1 | 292 | 0.0034 | 20 | c.514 others(37): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | TogoVar | |||||||
LAMC1_chr1_183018420_183150592 | 183140245 | C | CAAAAAAA others(13): Show |
intron_variant | MODIFIER | HG02109.hp2 HG02622.hp2 HG02809.hp1 others(3): Show |
a0001a0010a0013others(1): Show | a0001c0013a0001c0018a0010c0025others(2): Show | a0001c0013t0009a0001c0018t0010a0010c0025t0022others(2): Show | a0001c0013t0009g0244a0001c0013t0009g0245a0001c0018t0010g0138others(3): Show | 6 | 308 | 0.0195 | 20 | c.447 others(37): Show |
LAMC1 | ENSG00000135862.6 | transcript | ENST00000258341.5 | protein_coding | 26/27 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
LAMC1_chr1_183018420_183150592 | 183145732 | A | ATATATAT others(13): Show |
downstream_gene_variant | MODIFIER | HG01891.hp2 HG02896.hp2 HG03516.hp2 |
a0004 | a0004c0007 | a0004c0007t0005 | a0004c0007t0005g0122a0004c0007t0005g0216a0004c0007t0005g0218 | 3 | 308 | 0.0097 | 20 | c.*29 others(31): Show |
LAMC1 | ENSG00000135862.6 | transcript | ENST00000258341.5 | protein_coding | 141 | chr1 | TogoVar | |||||||
LAMC3_chr9_131004174_131099473 | 131022215 | A | AACACACA others(13): Show |
intron_variant | MODIFIER | HG00738.hp1 HG02109.hp1 HG03834.hp1 others(3): Show |
a0036a0043a0056others(3): Show | a0036c0156a0043c0033a0056c0208others(3): Show | a0036c0156t0001a0043c0033t0031a0056c0208t0023others(3): Show | a0036c0156t0001g0052a0043c0033t0031g0054a0056c0208t0023g0360others(3): Show | 6 | 360 | 0.0167 | 20 | c.374 others(37): Show |
LAMC3 | ENSG00000050555.19 | transcript | ENST00000361069.9 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
LAMC3_chr9_131004174_131099473 | 131046518 | A | ATTTTTTT others(13): Show |
intron_variant | MODIFIER | HG01981.hp2 | a0038 | a0038c0200 | a0038c0200t0005 | a0038c0200t0005g0097 | 1 | 360 | 0.0028 | 20 | c.151 others(37): Show |
LAMC3 | ENSG00000050555.19 | transcript | ENST00000361069.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
LAMC3_chr9_131004174_131099473 | 131047165 | C | CTTTTTTT others(13): Show |
intron_variant | MODIFIER | HG02647.hp1 | a0055 | a0055c0207 | a0055c0207t0001 | a0055c0207t0001g0356 | 1 | 360 | 0.0028 | 20 | c.151 others(39): Show |
LAMC3 | ENSG00000050555.19 | transcript | ENST00000361069.9 | protein_coding | 8/27 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
LAMC3_chr9_131004174_131099473 | 131096449 | A | AGGGGAGG others(13): Show |
downstream_gene_variant | MODIFIER | HG00738.hp1 HG01106.hp1 NA18970.hp2 others(4): Show |
a0001a0011a0014others(2): Show | a0001c0011a0011c0017a0014c0014others(2): Show | a0001c0011t0001a0011c0017t0001a0014c0014t0001others(2): Show | a0001c0011t0001g0077a0011c0017t0001g0102a0011c0017t0001g0316others(4): Show | 7 | 360 | 0.0194 | 20 | c.*46 others(31): Show |
LAMC3 | ENSG00000050555.19 | transcript | ENST00000361069.9 | protein_coding | 1977 | chr9 | TogoVar | |||||||
LAMP1_chr13_113292239_113328672 | 113324404 | G | GAAAGCAG others(13): Show |
downstream_gene_variant | MODIFIER | NA18984.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0235 | 1 | 354 | 0.0028 | 20 | c.*19 others(31): Show |
LAMP1 | ENSG00000185896.11 | transcript | ENST00000332556.5 | protein_coding | 733 | chr13 | TogoVar | |||||||
LAMP3_chr3_183117215_183167734 | 183149572 | A | AATATATA others(13): Show |
intron_variant | MODIFIER | NA18941.hp2 | a0001 | a0001c0003 | a0001c0003t0002 | a0001c0003t0002g0050 | 1 | 372 | 0.0027 | 20 | c.888 others(37): Show |
LAMP3 | ENSG00000078081.8 | transcript | ENST00000265598.8 | protein_coding | 3/5 | chr3 | TogoVar | |||||||
LAMP3_chr3_183117215_183167734 | 183149574 | A | AATATATA others(13): Show |
intron_variant | MODIFIER | HG02165.hp2 NA18962.hp2 |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0002 | a0001c0003t0001g0112a0001c0003t0002g0052 | 2 | 372 | 0.0054 | 20 | c.888 others(37): Show |
LAMP3 | ENSG00000078081.8 | transcript | ENST00000265598.8 | protein_coding | 3/5 | chr3 | TogoVar | |||||||
LAMP5_chr20_9509590_9535524 | 9517621 | A | ATGTGTGT others(13): Show |
intron_variant | MODIFIER | HG01081.hp1 HG02258.hp2 HG02976.hp1 |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0002a0002c0002t0003 | a0002c0002t0001g0364a0002c0002t0002g0363a0002c0002t0003g0307 | 3 | 448 | 0.0067 | 20 | c.476 others(35): Show |
LAMP5 | ENSG00000125869.10 | transcript | ENST00000246070.3 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
LAMP5_chr20_9509590_9535524 | 9526860 | G | GTATATAT others(13): Show |
intron_variant | MODIFIER | NA19000.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0152 | 1 | 448 | 0.0022 | 20 | c.665 others(37): Show |
LAMP5 | ENSG00000125869.10 | transcript | ENST00000246070.3 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
LAMTOR3_chr4_99873336_99899427 | 99886918 | A | ATGTATGT others(13): Show |
intron_variant | MODIFIER | HG00735.hp2 HG02809.hp1 |
a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0094a0001c0001t0003g0097 | 2 | 384 | 0.0052 | 20 | c.103 others(35): Show |
LAMTOR3 | ENSG00000109270.13 | transcript | ENST00000499666.7 | protein_coding | 4/6 | chr4 | TogoVar | |||||||
LANCL1_chr2_210426251_210481759 | 210474739 | A | AAAATAAA others(13): Show |
intron_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(49): Show |
a0001a0006 | a0001c0001a0006c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0016others(5): Show | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(30): Show | 52 | 358 | 0.1453 | 20 | c.81+ others(35): Show |
LANCL1 | ENSG00000115365.13 | transcript | ENST00000450366.7 | protein_coding | 2/9 | chr2 | TogoVar | |||||||
LANCL2_chr7_55360337_55438737 | 55415621 | C | CTTTTTTT others(13): Show |
intron_variant | MODIFIER | HG00621.hp1 HG01175.hp2 HG01192.hp1 others(14): Show |
a0001a0002 | a0001c0004a0002c0003 | a0001c0004t0002a0001c0004t0013a0001c0004t0025others(2): Show | a0001c0004t0002g0183a0001c0004t0013g0032a0001c0004t0013g0033others(14): Show | 17 | 352 | 0.0483 | 20 | c.100 others(39): Show |
LANCL2 | ENSG00000132434.10 | transcript | ENST00000254770.3 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
LAP3_chr4_17572198_17612970 | 17573730 | G | GTGTGTGT others(13): Show |
upstream_gene_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0171 | 1 | 300 | 0.0033 | 20 | c.-37 others(31): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 3467 | chr4 | TogoVar | |||||||
LAP3_chr4_17572198_17612970 | 17573730 | G | GTGTGTGT others(13): Show |
upstream_gene_variant | MODIFIER | HG01192.hp2 HG03831.hp2 NA18945.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0011 | a0001c0001t0004g0003a0001c0001t0004g0017a0001c0001t0004g0220others(2): Show | 7 | 300 | 0.0233 | 20 | c.-37 others(31): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 3467 | chr4 | TogoVar | |||||||
LAPTM4B_chr8_97770788_97858013 | 97832676 | T | TTTTTATT others(13): Show |
intron_variant | MODIFIER | HG00558.hp2 HG02109.hp2 HG02257.hp2 others(7): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0003a0001c0001t0008a0002c0003t0013 | a0001c0001t0003g0314a0001c0001t0008g0020a0001c0001t0008g0022others(7): Show | 10 | 380 | 0.0263 | 20 | c.603 others(37): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
LAPTM4B_chr8_97770788_97858013 | 97834144 | G | GAAAAAAA others(13): Show |
intron_variant | MODIFIER | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(25): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(2): Show | a0001c0001t0001g0052a0001c0001t0001g0092a0001c0001t0001g0094others(25): Show | 28 | 380 | 0.0737 | 20 | c.603 others(37): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
LAPTM4B_chr8_97770788_97858013 | 97843780 | C | CAAATAAA others(13): Show |
intron_variant | MODIFIER | NA18954.hp2 NA19087.hp2 NA19088.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0273a0001c0001t0001g0291a0001c0001t0001g0298 | 3 | 380 | 0.0079 | 20 | c.604 others(37): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
LAPTM4B_chr8_97770788_97858013 | 97850465 | G | GGGGTGTG others(13): Show |
intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0003 | 1 | 380 | 0.0026 | 20 | c.604 others(35): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
LAPTM4B_chr8_97770788_97858013 | 97850474 | G | GTGTGTGT others(13): Show |
intron_variant | MODIFIER | HG01884.hp2 HG02109.hp2 HG02257.hp2 others(12): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(1): Show | a0001c0001t0003g0077a0001c0001t0007g0172a0001c0001t0007g0199others(12): Show | 15 | 380 | 0.0395 | 20 | c.604 others(35): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
LAPTM4B_chr8_97770788_97858013 | 97850476 | G | GTGTGTGT others(13): Show |
intron_variant | MODIFIER | NA18980.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0313 | 1 | 380 | 0.0026 | 20 | c.604 others(35): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | TogoVar |