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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
KNDC1_chr10_133155219_133231412 | 133223322 | T | TGTGTGTG others(33): Show |
intron_variant | MODIFIER | HG03130.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0239 | 1 | 332 | 0.0030 | 40 | c.501 others(59): Show |
KNDC1 | ENSG00000171798.19 | transcript | ENST00000304613.8 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
KNTC1_chr12_122522249_122631396 | 122541287 | G | GCCTGCCT others(33): Show |
intron_variant | MODIFIER | HG03471.hp1 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0124 | 1 | 320 | 0.0031 | 40 | c.446 others(55): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
KNTC1_chr12_122522249_122631396 | 122541287 | G | GCCTGCCT others(33): Show |
intron_variant | MODIFIER | HG02280.hp2 | a0011 | a0011c0015 | a0011c0015t0001 | a0011c0015t0001g0274 | 1 | 320 | 0.0031 | 40 | c.446 others(55): Show |
KNTC1 | ENSG00000184445.12 | transcript | ENST00000333479.12 | protein_coding | 5/63 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
KPNA1_chr3_122416902_122519939 | 122452564 | G | GGGAGGGA others(33): Show |
intron_variant | MODIFIER | HG02040.hp2 | a0001 | a0001c0001 | a0001c0001t0034 | a0001c0001t0034g0324 | 1 | 400 | 0.0025 | 40 | c.565 others(55): Show |
KPNA1 | ENSG00000114030.13 | transcript | ENST00000344337.11 | protein_coding | 6/13 | chr3 | TogoVar | ||||||
KPNA1_chr3_122416902_122519939 | 122452564 | G | GGGAGGGA others(33): Show |
intron_variant | MODIFIER | HG03688.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0299 | 1 | 400 | 0.0025 | 40 | c.565 others(55): Show |
KPNA1 | ENSG00000114030.13 | transcript | ENST00000344337.11 | protein_coding | 6/13 | chr3 | TogoVar | ||||||
KPNA1_chr3_122416902_122519939 | 122452572 | G | GGGAGGGA others(33): Show |
intron_variant | MODIFIER | NA18999.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0346 | 1 | 400 | 0.0025 | 40 | c.565 others(55): Show |
KPNA1 | ENSG00000114030.13 | transcript | ENST00000344337.11 | protein_coding | 6/13 | chr3 | TogoVar | ||||||
KRBA1_chr7_149709951_149739575 | 149738218 | A | ATATATAT others(33): Show |
downstream_gene_variant | MODIFIER | HG02723.hp2 HG02895.hp2 |
a0006 | a0006c0008 | a0006c0008t0003 | a0006c0008t0003g0032a0006c0008t0003g0046 | 2 | 414 | 0.0048 | 40 | c.*41 others(51): Show |
KRBA1 | ENSG00000133619.18 | transcript | ENST00000496259.6 | protein_coding | 3644 | chr7 | TogoVar | ||||||
KREMEN1_chr22_29068035_29151820 | 29131718 | G | GTATATAT others(33): Show |
intron_variant | MODIFIER | HG00621.hp2 HG01928.hp1 HG01993.hp1 |
a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0171a0001c0001t0012g0172a0001c0001t0012g0339 | 3 | 368 | 0.0082 | 40 | c.632 others(57): Show |
KREMEN1 | ENSG00000183762.13 | transcript | ENST00000400335.9 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
KRT40_chr17_40972715_40989326 | 40974458 | G | GTTTCTTT others(33): Show |
downstream_gene_variant | MODIFIER | HG03139.hp2 | a0006 | a0006c0006 | a0006c0006t0002 | a0006c0006t0002g0006 | 1 | 451 | 0.0022 | 40 | c.*37 others(51): Show |
KRT40 | ENSG00000204889.11 | transcript | ENST00000377755.9 | protein_coding | 3256 | chr17 | TogoVar | ||||||
KRTAP16-1_chr17_41302700_41314309 | 41310389 | G | GAAAGAAA others(33): Show |
upstream_gene_variant | MODIFIER | HG01943.hp2 HG02027.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | 2 | 421 | 0.0048 | 40 | c.-11 others(51): Show |
KRTAP16-1 | ENSG00000212657.2 | transcript | ENST00000391352.2 | protein_coding | 1081 | chr17 | TogoVar | ||||||
KRTAP16-1_chr17_41302700_41314309 | 41310389 | G | GAAAGAAA others(33): Show |
upstream_gene_variant | MODIFIER | NA18985.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | 1 | 421 | 0.0024 | 40 | c.-11 others(51): Show |
KRTAP16-1 | ENSG00000212657.2 | transcript | ENST00000391352.2 | protein_coding | 1081 | chr17 | TogoVar | ||||||
KRTAP16-1_chr17_41302700_41314309 | 41310389 | G | GAAAGAAA others(33): Show |
upstream_gene_variant | MODIFIER | NA18975.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | 1 | 421 | 0.0024 | 40 | c.-11 others(51): Show |
KRTAP16-1 | ENSG00000212657.2 | transcript | ENST00000391352.2 | protein_coding | 1081 | chr17 | TogoVar | ||||||
KRTAP17-1_chr17_41309912_41320710 | 41310389 | G | GAAAGAAA others(33): Show |
downstream_gene_variant | MODIFIER | HG01943.hp1 HG02027.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | 2 | 413 | 0.0048 | 40 | c.*49 others(51): Show |
KRTAP17-1 | ENSG00000186860.5 | transcript | ENST00000334202.5 | protein_coding | 4522 | chr17 | TogoVar | ||||||
KRTAP17-1_chr17_41309912_41320710 | 41310389 | G | GAAAGAAA others(33): Show |
downstream_gene_variant | MODIFIER | NA18975.hp2 NA18977.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | 2 | 413 | 0.0048 | 40 | c.*49 others(51): Show |
KRTAP17-1 | ENSG00000186860.5 | transcript | ENST00000334202.5 | protein_coding | 4522 | chr17 | TogoVar | ||||||
KRTAP19-7_chr21_30555875_30566314 | 30562392 | T | TATATATA others(33): Show |
upstream_gene_variant | MODIFIER | HG02647.hp1 HG03225.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | 2 | 422 | 0.0047 | 40 | c.-11 others(51): Show |
KRTAP19-7 | ENSG00000244362.3 | transcript | ENST00000334849.2 | protein_coding | 1079 | chr21 | TogoVar | ||||||
KRTAP5-1_chr11_1579342_1590283 | 1583879 | G | GGTGTGTG others(33): Show |
downstream_gene_variant | MODIFIER | HG01496.hp1 HG03486.hp1 NA18969.hp1 others(2): Show |
a0002a0003a0005 | a0002c0002a0003c0003a0005c0005 | a0002c0002t0001a0003c0003t0001a0005c0005t0001 | a0002c0002t0001g0000a0003c0003t0001g0000a0005c0005t0001g0000 | 5 | 429 | 0.0117 | 40 | c.*53 others(49): Show |
KRTAP5-1 | ENSG00000205869.2 | transcript | ENST00000382171.2 | protein_coding | 462 | chr11 | TogoVar | ||||||
KRTAP9-6_chr17_41260378_41270860 | 41263222 | T | TGAAGGAA others(33): Show |
upstream_gene_variant | MODIFIER | HG02965.hp2 | a0000 | a0000c0001 | a0000c0001t0000 | a0000c0001t0000g0000 | 1 | 248 | 0.0040 | 40 | c.-21 others(51): Show |
KRTAP9-6 | ENSG00000212659.2 | transcript | ENST00000391355.2 | protein_coding | 2155 | chr17 | TogoVar | ||||||
KSR1_chr17_27451448_27631435 | 27526044 | T | TTTCTTTT others(33): Show |
intron_variant | MODIFIER | HG03130.hp2 | a0001 | a0001c0006 | a0001c0006t0012 | a0001c0006t0012g0132 | 1 | 246 | 0.0041 | 40 | c.232 others(59): Show |
KSR1 | ENSG00000141068.17 | transcript | ENST00000644974.2 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
KSR2_chr12_117448012_117973990 | 117606391 | C | CCCTCCCT others(33): Show |
intron_variant | MODIFIER | HG02723.hp2 | a0001 | a0001c0001 | a0001c0001t0134 | a0001c0001t0134g0121 | 1 | 196 | 0.0051 | 40 | c.117 others(61): Show |
KSR2 | ENSG00000171435.15 | transcript | ENST00000339824.7 | protein_coding | 5/19 | chr12 | TogoVar | ||||||
KSR2_chr12_117448012_117973990 | 117606481 | T | TCTCCTTC others(33): Show |
intron_variant | MODIFIER | HG00323.hp2 HG01109.hp2 HG01192.hp1 others(10): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0020a0001c0001t0021a0001c0001t0030others(10): Show | a0001c0001t0020g0171a0001c0001t0021g0164a0001c0001t0030g0025others(10): Show | 13 | 196 | 0.0663 | 40 | c.117 others(61): Show |
KSR2 | ENSG00000171435.15 | transcript | ENST00000339824.7 | protein_coding | 5/19 | chr12 | TogoVar | ||||||
KTN1_chr14_55575207_55689579 | 55646460 | T | TTTTCCTT others(33): Show |
intron_variant | MODIFIER | HG00323.hp2 HG03669.hp1 NA18985.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0009 | a0001c0001t0001g0156a0001c0001t0001g0198a0001c0001t0009g0260 | 3 | 314 | 0.0096 | 40 | c.217 others(57): Show |
KTN1 | ENSG00000126777.18 | transcript | ENST00000395314.8 | protein_coding | 18/43 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
KYNU_chr2_142872664_143060833 | 142977372 | G | GATATATA others(33): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0042 | 1 | 332 | 0.0030 | 40 | c.730 others(57): Show |
KYNU | ENSG00000115919.15 | transcript | ENST00000264170.9 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
L3MBTL4_chr18_5949717_6419911 | 6099585 | A | AATATATA others(33): Show |
intron_variant | MODIFIER | HG04115.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0025 | 1 | 94 | 0.0106 | 40 | c.120 others(59): Show |
L3MBTL4 | ENSG00000154655.16 | transcript | ENST00000317931.12 | protein_coding | 14/18 | chr18 | TogoVar | ||||||
LAMA2_chr6_128878138_129521566 | 128879455 | A | ATATATAT others(33): Show |
upstream_gene_variant | MODIFIER | HG00140.hp2 HG01074.hp1 HG03688.hp1 others(6): Show |
a0001a0007a0013others(2): Show | a0001c0001a0001c0012a0001c0067others(6): Show | a0001c0001t0001a0001c0012t0001a0001c0067t0001others(6): Show | a0001c0001t0001g0070a0001c0012t0001g0074a0001c0067t0001g0073others(6): Show | 9 | 88 | 0.1023 | 40 | c.-37 others(51): Show |
LAMA2 | ENSG00000196569.14 | transcript | ENST00000421865.3 | protein_coding | 3682 | chr6 | TogoVar | ||||||
LAMA2_chr6_128878138_129521566 | 129205478 | G | GTATATAT others(33): Show |
intron_variant | MODIFIER | HG06807.hp1 | a0003 | a0003c0020 | a0003c0020t0008 | a0003c0020t0008g0027 | 1 | 88 | 0.0114 | 40 | c.178 others(61): Show |
LAMA2 | ENSG00000196569.14 | transcript | ENST00000421865.3 | protein_coding | 12/64 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
LAMA3_chr18_23684453_23960066 | 23687746 | T | TTGTGTGT others(33): Show |
upstream_gene_variant | MODIFIER | HG03471.hp1 NA18747.hp2 NA18955.hp2 others(3): Show |
a0002a0003a0035 | a0002c0003a0003c0004a0035c0058 | a0002c0003t0001a0003c0004t0001a0035c0058t0001 | a0002c0003t0001g0279a0003c0004t0001g0248a0003c0004t0001g0260others(3): Show | 6 | 280 | 0.0214 | 40 | c.-19 others(51): Show |
LAMA3 | ENSG00000053747.17 | transcript | ENST00000313654.14 | protein_coding | 1706 | chr18 | TogoVar | ||||||
LAMA5_chr20_62304065_62372312 | 62360517 | G | GGGTGGAG others(33): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0095 | a0095c0136 | a0095c0136t0001 | a0095c0136t0001g0186 | 1 | 186 | 0.0054 | 40 | c.450 others(57): Show |
LAMA5 | ENSG00000130702.15 | transcript | ENST00000252999.7 | protein_coding | 2/79 | chr20 | TogoVar | ||||||
LAMB1_chr7_107918799_108008161 | 107976861 | T | TTCCTTCC others(33): Show |
intron_variant | MODIFIER | HG02559.hp2 NA18962.hp2 NA19057.hp1 |
a0001a0027 | a0001c0002a0001c0007a0027c0061 | a0001c0002t0001a0001c0007t0001a0027c0061t0001 | a0001c0002t0001g0122a0001c0007t0001g0007a0027c0061t0001g0123 | 3 | 364 | 0.0082 | 40 | c.100 others(57): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | TogoVar | ||||||
LAMB1_chr7_107918799_108008161 | 107976948 | C | CCTCCTTC others(33): Show |
intron_variant | MODIFIER | NA18612.hp1 NA18953.hp2 NA18981.hp1 others(2): Show |
a0003 | a0003c0004 | a0003c0004t0001 | a0003c0004t0001g0079a0003c0004t0001g0080a0003c0004t0001g0157others(2): Show | 5 | 364 | 0.0137 | 40 | c.100 others(59): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | TogoVar | ||||||
LAMC1_chr1_183018420_183150592 | 183077776 | G | GTGTGTGT others(33): Show |
intron_variant | MODIFIER | HG01074.hp2 HG01109.hp1 |
a0001 | a0001c0002a0001c0034 | a0001c0002t0002a0001c0034t0002 | a0001c0002t0002g0027a0001c0034t0002g0087 | 2 | 308 | 0.0065 | 40 | c.419 others(59): Show |
LAMC1 | ENSG00000135862.6 | transcript | ENST00000258341.5 | protein_coding | 1/27 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
LANCL2_chr7_55360337_55438737 | 55402744 | C | CGCTCCTC others(33): Show |
intron_variant | MODIFIER | HG01891.hp2 HG01993.hp2 HG02055.hp1 others(14): Show |
a0001a0004 | a0001c0004a0004c0006 | a0001c0004t0002a0001c0004t0006a0004c0006t0006 | a0001c0004t0002g0183a0001c0004t0006g0176a0001c0004t0006g0177others(14): Show | 17 | 352 | 0.0483 | 40 | c.825 others(57): Show |
LANCL2 | ENSG00000132434.10 | transcript | ENST00000254770.3 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
LAPTM4B_chr8_97770788_97858013 | 97834144 | G | GAAAAAAA others(33): Show |
intron_variant | MODIFIER | HG00639.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0180 | 1 | 380 | 0.0026 | 40 | c.603 others(57): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
LAPTM4B_chr8_97770788_97858013 | 97840771 | T | TGCTCCTC others(33): Show |
intron_variant | MODIFIER | HG00099.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0192 | 1 | 380 | 0.0026 | 40 | c.604 others(59): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
LAPTM4B_chr8_97770788_97858013 | 97841153 | T | TGGGCAGA others(33): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(257): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0018others(257): Show | 260 | 380 | 0.6842 | 40 | c.604 others(59): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
LAPTM4B_chr8_97770788_97858013 | 97841153 | T | TGGGTAGA others(33): Show |
intron_variant | MODIFIER | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(21): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(9): Show | a0001c0001t0002g0142a0001c0001t0002g0143a0001c0001t0003g0077others(21): Show | 24 | 380 | 0.0632 | 40 | c.604 others(59): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
LAPTM4B_chr8_97770788_97858013 | 97841164 | G | GCTCCTCA others(33): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0120 | 1 | 380 | 0.0026 | 40 | c.604 others(59): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
LAPTM4B_chr8_97770788_97858013 | 97841172 | C | CTTCCCAG others(33): Show |
intron_variant | MODIFIER | NA18954.hp2 NA19087.hp2 NA19088.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0273a0001c0001t0001g0291a0001c0001t0001g0298 | 3 | 380 | 0.0079 | 40 | c.604 others(59): Show |
LAPTM4B | ENSG00000104341.17 | transcript | ENST00000521545.7 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
LARP1B_chr4_128056312_128216988 | 128098747 | G | GTGTGTAT others(33): Show |
intron_variant | MODIFIER | HG01099.hp1 HG02080.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0180a0001c0001t0001g0275 | 2 | 336 | 0.0060 | 40 | c.813 others(55): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
LARP1B_chr4_128056312_128216988 | 128098747 | G | GTGTGTGT others(33): Show |
intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0131 | 1 | 336 | 0.0030 | 40 | c.813 others(55): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
LARP1B_chr4_128056312_128216988 | 128098747 | G | GTGTGTGT others(33): Show |
intron_variant | MODIFIER | HG00438.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0259 | 1 | 336 | 0.0030 | 40 | c.813 others(55): Show |
LARP1B | ENSG00000138709.20 | transcript | ENST00000326639.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
LARP4_chr12_50395885_50485004 | 50446360 | T | TCTCTCTC others(33): Show |
intron_variant | MODIFIER | HG03579.hp2 NA18969.hp1 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0008a0003c0003t0001 | a0001c0001t0008g0184a0003c0003t0001g0166 | 2 | 318 | 0.0063 | 40 | c.804 others(57): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
LARP4_chr12_50395885_50485004 | 50446364 | T | TCTCTCTC others(33): Show |
intron_variant | MODIFIER | HG02055.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0169 | 1 | 318 | 0.0031 | 40 | c.804 others(57): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
LARP4_chr12_50395885_50485004 | 50446364 | T | TCTCTCTC others(33): Show |
intron_variant | MODIFIER | HG01169.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0164 | 1 | 318 | 0.0031 | 40 | c.804 others(57): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
LARP4_chr12_50395885_50485004 | 50446366 | T | TCTCTCTC others(33): Show |
intron_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0178 | 1 | 318 | 0.0031 | 40 | c.804 others(57): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | |||||
LAT2_chr7_74205006_74234834 | 74214545 | T | TATATATA others(33): Show |
intron_variant | MODIFIER | homoSapiens_chm13v2.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0319 | 1 | 344 | 0.0029 | 40 | c.-21 others(57): Show |
LAT2 | ENSG00000086730.17 | transcript | ENST00000460943.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
LATS2_chr13_20968036_21066586 | 21050125 | C | CAGACAGA others(33): Show |
intron_variant | MODIFIER | NA20129.hp2 | a0004 | a0004c0004 | a0004c0004t0004 | a0004c0004t0004g0298 | 1 | 316 | 0.0032 | 40 | c.-20 others(59): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | TogoVar | ||||||
LATS2_chr13_20968036_21066586 | 21050147 | G | GATAGATA others(33): Show |
intron_variant | MODIFIER | HG00597.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0224 | 1 | 316 | 0.0032 | 40 | c.-20 others(59): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | TogoVar | ||||||
LATS2_chr13_20968036_21066586 | 21050147 | G | GATAGATA others(33): Show |
intron_variant | MODIFIER | HG02738.hp2 | a0004 | a0004c0004 | a0004c0004t0045 | a0004c0004t0045g0314 | 1 | 316 | 0.0032 | 40 | c.-20 others(59): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | TogoVar | ||||||
LATS2_chr13_20968036_21066586 | 21050147 | G | GATAGATA others(33): Show |
intron_variant | MODIFIER | HG01074.hp1 HG01257.hp2 HG03139.hp1 others(2): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0001a0002c0002t0003a0003c0003t0007others(1): Show | a0001c0001t0001g0272a0002c0002t0003g0098a0003c0003t0007g0312others(2): Show | 5 | 316 | 0.0158 | 40 | c.-20 others(59): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | TogoVar | ||||||
LATS2_chr13_20968036_21066586 | 21050147 | G | GATAGATA others(33): Show |
intron_variant | MODIFIER | HG01106.hp1 HG01255.hp1 HG01496.hp1 others(7): Show |
a0001a0004a0005others(1): Show | a0001c0001a0004c0004a0005c0016others(1): Show | a0001c0001t0001a0004c0004t0005a0004c0004t0025others(2): Show | a0001c0001t0001g0092a0001c0001t0001g0264a0001c0001t0001g0265others(7): Show | 10 | 316 | 0.0317 | 40 | c.-20 others(59): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | TogoVar |