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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
KRTAP16-1_chr17_41302700_41314309 | 41310389 | G | GAAAGAAA others(33): Show |
upstream_gene_variant | MODIFIER | NA18975.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | 1 | 254 | 0.0039 | 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 | 254 | 0.0079 | 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 | 254 | 0.0079 | 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 | 403 | 0.0050 | 40 | c.-11 others(51): Show |
KRTAP19-7 | ENSG00000244362.3 | transcript | ENST00000334849.2 | protein_coding | 1079 | chr21 | TogoVar | |||||||
KRTAP4-9_chr17_41100389_41111488 | 41110054 | C | CAAGAAAG others(33): Show |
downstream_gene_variant | MODIFIER | HG00438.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | 1 | 130 | 0.0077 | 40 | c.*40 others(51): Show |
KRTAP4-9 | ENSG00000212722.9 | transcript | ENST00000391415.2 | protein_coding | 3567 | chr17 | TogoVar | |||||||
KRTAP4-9_chr17_41100389_41111488 | 41110054 | C | CAAGCAAG others(33): Show |
downstream_gene_variant | MODIFIER | HG02109.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0000 | 1 | 130 | 0.0077 | 40 | c.*40 others(51): Show |
KRTAP4-9 | ENSG00000212722.9 | transcript | ENST00000391415.2 | protein_coding | 3567 | chr17 | 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 |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0004 | a0001c0001t0001a0002c0002t0001a0004c0004t0001 | a0001c0001t0001g0000 a0002c0002t0001g0000 a0004c0004t0001g0000 |
5 | 121 | 0.0413 | 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 | a0001 | a0001c0001 | a0001c0001t0000 | a0001c0001t0000g0000 | 1 | 15 | 0.0667 | 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 | 103 | 0.0097 | 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 | a0001c0001t0117 | a0001c0001t0117g0121 | 1 | 182 | 0.0055 | 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 | a0001c0001t0002a0001c0001t0023a0001c0001t0032others(10): Show | a0001c0001t0002g0164 a0001c0001t0023g0171 a0001c0001t0032g0025 others(10): Show |
13 | 135 | 0.0963 | 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 | a0001c0001t0001g0154 a0001c0001t0001g0196 a0001c0001t0009g0259 |
3 | 123 | 0.0244 | 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 | a0001c0001t0006 | a0001c0001t0006g0044 | 1 | 160 | 0.0063 | 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 | 2 | 0.5000 | 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(5): Show |
a0001a0006a0015others(2): Show | a0001c0012a0001c0067a0001c0068others(5): Show | a0001c0012t0001a0001c0067t0001a0001c0068t0003others(5): Show | a0001c0012t0001g0068 a0001c0067t0001g0070 a0001c0068t0003g0067 others(5): Show |
8 | 83 | 0.0964 | 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 | a0004 | a0004c0020 | a0004c0020t0008 | a0004c0020t0008g0027 | 1 | 53 | 0.0189 | 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 |
a0002a0003a0030 | a0002c0003a0003c0004a0030c0058 | a0002c0003t0001a0003c0004t0001a0030c0058t0001 | a0002c0003t0001g0279 a0003c0004t0001g0248 a0003c0004t0001g0260 others(3): Show |
6 | 132 | 0.0455 | 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 | a0082 | a0082c0135 | a0082c0135t0001 | a0082c0135t0001g0186 | 1 | 155 | 0.0065 | 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 |
a0001a0025 | a0001c0002a0001c0007a0025c0061 | a0001c0002t0001a0001c0007t0001a0025c0061t0001 | a0001c0002t0001g0118 a0001c0007t0001g0007 a0025c0061t0001g0119 |
3 | 237 | 0.0127 | 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 | a0003c0004t0001g0079 a0003c0004t0001g0080 a0003c0004t0001g0157 others(2): Show |
5 | 284 | 0.0176 | 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 | a0001c0002t0002g0031 a0001c0034t0002g0089 |
2 | 130 | 0.0154 | 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 | a0001c0004t0002g0184 a0001c0004t0006g0177 a0001c0004t0006g0178 others(14): Show |
17 | 269 | 0.0632 | 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 | a0001c0001t0010g0179 | 1 | 196 | 0.0051 | 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 | a0001c0001t0004g0191 | 1 | 378 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0017 others(257): Show |
260 | 354 | 0.7345 | 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 | a0001c0001t0002g0141 a0001c0001t0002g0142 a0001c0001t0003g0076 others(21): Show |
24 | 118 | 0.2034 | 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 | a0001c0001t0006g0119 | 1 | 378 | 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 | a0001c0001t0001g0273 a0001c0001t0001g0291 a0001c0001t0001g0298 |
3 | 378 | 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 | a0001c0001t0001g0177 a0001c0001t0001g0275 |
2 | 160 | 0.0125 | 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 | a0001c0001t0007g0132 | 1 | 159 | 0.0063 | 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 | 159 | 0.0063 | 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 | a0001c0001t0008g0185 a0003c0003t0001g0167 |
2 | 291 | 0.0069 | 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 | a0001c0001t0004g0170 | 1 | 296 | 0.0034 | 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 | a0001c0001t0001g0165 | 1 | 296 | 0.0034 | 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 | a0001c0001t0001g0179 | 1 | 282 | 0.0035 | 40 | c.804 others(57): Show |
LARP4 | ENSG00000161813.23 | transcript | ENST00000398473.7 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | TogoVar | ||||||
LATS2_chr13_20968036_21066586 | 21050125 | C | CAGACAGA others(33): Show |
intron_variant | MODIFIER | NA20129.hp2 | a0004 | a0004c0004 | a0004c0004t0004 | a0004c0004t0004g0296 | 1 | 285 | 0.0035 | 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 | a0001c0001t0001g0222 | 1 | 55 | 0.0182 | 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 | a0004c0004t0045g0312 | 1 | 55 | 0.0182 | 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 | a0001c0001t0001g0270 a0002c0002t0003g0098 a0003c0003t0007g0310 others(2): Show |
5 | 59 | 0.0847 | 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 | a0001c0001t0001g0092 a0001c0001t0001g0262 a0001c0001t0001g0264 others(7): Show |
10 | 64 | 0.1563 | 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 | HG00423.hp1 HG00642.hp1 HG01070.hp1 others(26): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(7): Show | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0195 others(26): Show |
29 | 83 | 0.3494 | 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 | NA19004.hp2 NA19065.hp2 NA19087.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0010 | a0001c0001t0002g0002 a0001c0001t0002g0166 a0002c0002t0010g0279 |
4 | 58 | 0.0690 | 40 | c.-20 others(59): Show |
LATS2 | ENSG00000150457.9 | transcript | ENST00000382592.5 | protein_coding | 1/7 | chr13 | TogoVar | |||||||
LAX1_chr1_203760183_203781372 | 203770433 | A | AAGAGAGA others(33): Show |
intron_variant | MODIFIER | NA18975.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0208 | 1 | 153 | 0.0065 | 40 | c.90- others(53): Show |
LAX1 | ENSG00000122188.13 | transcript | ENST00000442561.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
LCK_chr1_32246265_32291165 | 32272623 | A | AAGAGAGA others(33): Show |
intron_variant | MODIFIER | HG02257.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0183 | 1 | 255 | 0.0039 | 40 | c.-5- others(55): Show |
LCK | ENSG00000182866.18 | transcript | ENST00000336890.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
LCLAT1_chr2_30442246_30649225 | 30638782 | T | TTCTCCCA others(33): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00642.hp1 others(30): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0031a0001c0001t0063others(4): Show | a0001c0001t0004g0261 a0001c0001t0004g0262 a0001c0001t0004g0263 others(30): Show |
33 | 271 | 0.1218 | 40 | c.629 others(57): Show |
LCLAT1 | ENSG00000172954.14 | transcript | ENST00000379509.8 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
LCMT2_chr15_43318649_43335573 | 43334633 | T | TTATATAT others(33): Show |
upstream_gene_variant | MODIFIER | NA19075.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0000 | 1 | 19 | 0.0526 | 40 | c.-41 others(51): Show |
LCMT2 | ENSG00000168806.8 | transcript | ENST00000305641.7 | protein_coding | 4061 | chr15 | TogoVar | |||||||
LCN10_chr9_136733170_136747940 | 136746217 | G | GGGGGAAA others(33): Show |
upstream_gene_variant | MODIFIER | HG02965.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 390 | 0.0026 | 40 | c.-33 others(51): Show |
LCN10 | ENSG00000187922.14 | transcript | ENST00000497771.6 | protein_coding | 3278 | chr9 | TogoVar | |||||||
LCN15_chr9_136754634_136769518 | 136769471 | C | CGCCACCC others(33): Show |
upstream_gene_variant | MODIFIER | HG02109.hp2 | a0002 | a0002c0004 | a0002c0004t0001 | a0002c0004t0001g0011 | 1 | 353 | 0.0028 | 40 | c.-49 others(51): Show |
LCN15 | ENSG00000177984.7 | transcript | ENST00000316144.6 | protein_coding | 4954 | chr9 | TogoVar | |||||||
LCP2_chr5_170241233_170302777 | 170268880 | C | CATGCACA others(33): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(214): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(34): Show | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(211): Show |
217 | 348 | 0.6236 | 40 | c.524 others(55): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | TogoVar | |||||||
LDAH_chr2_20679031_20828101 | 20710606 | G | GTGTGTAT others(33): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0242 | 1 | 237 | 0.0042 | 40 | c.704 others(57): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | TogoVar |