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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
HSD17B3_chr9_96230306_96307176 | 96300253 | C | CACACACA others(4): Show |
intron_variant | MODIFIER | HG00738.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0213 | 1 | 374 | 0.0027 | 11 | c.154 others(28): Show |
HSD17B3 | ENSG00000130948.10 | transcript | ENST00000375263.8 | protein_coding | 1/10 | chr9 | TogoVar | ||||||
HSD17B4_chr5_119447497_119547332 | 119494325 | T | TTTCTTTC others(4): Show |
intron_variant | MODIFIER | NA18972.hp2 | a0005 | a0005c0005 | a0005c0005t0001 | a0005c0005t0001g0266 | 1 | 380 | 0.0026 | 11 | c.868 others(26): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
HSD17B4_chr5_119447497_119547332 | 119494390 | T | TTTCTTTC others(4): Show |
intron_variant | MODIFIER | HG04199.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0283 | 1 | 380 | 0.0026 | 11 | c.868 others(26): Show |
HSD17B4 | ENSG00000133835.18 | transcript | ENST00000510025.7 | protein_coding | 11/23 | chr5 | TogoVar | ||||||
HSD3B7_chr16_30980207_30994147 | 30992693 | G | GGGGGTGG others(4): Show |
downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0002c0004others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(15): Show | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(25): Show | 306 | 314 | 0.9745 | 11 | c.*45 others(22): Show |
HSD3B7 | ENSG00000099377.14 | transcript | ENST00000297679.10 | protein_coding | 3547 | chr16 | TogoVar | ||||||
HSDL1_chr16_84117141_84150177 | 84148596 | C | CTCTCTTT others(4): Show |
upstream_gene_variant | MODIFIER | HG02895.hp2 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0209 | 1 | 448 | 0.0022 | 11 | c.-35 others(22): Show |
HSDL1 | ENSG00000103160.12 | transcript | ENST00000219439.9 | protein_coding | 3420 | chr16 | TogoVar | ||||||
HSDL1_chr16_84117141_84150177 | 84148596 | C | CTTTTTTT others(4): Show |
upstream_gene_variant | MODIFIER | HG02165.hp1 | a0001 | a0001c0001 | a0001c0001t0032 | a0001c0001t0032g0091 | 1 | 448 | 0.0022 | 11 | c.-35 others(22): Show |
HSDL1 | ENSG00000103160.12 | transcript | ENST00000219439.9 | protein_coding | 3420 | chr16 | TogoVar | ||||||
HSDL2_chr9_112375108_112477405 | 112474100 | C | CATCATCT others(4): Show |
downstream_gene_variant | MODIFIER | HG00733.hp2 HG02080.hp2 NA18957.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0075a0001c0001t0001g0303a0001c0001t0002g0240others(1): Show | 4 | 366 | 0.0109 | 11 | c.*35 others(22): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 1696 | chr9 | TogoVar | ||||||
HSDL2_chr9_112375108_112477405 | 112476260 | G | GCCCCCCC others(4): Show |
downstream_gene_variant | MODIFIER | NA19003.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0069 | 1 | 366 | 0.0027 | 11 | c.*57 others(22): Show |
HSDL2 | ENSG00000119471.15 | transcript | ENST00000398805.8 | protein_coding | 3856 | chr9 | TogoVar | ||||||
HSF1_chr8_144286604_144319720 | 144313736 | G | GCCCCGCC others(4): Show |
intron_variant | MODIFIER | HG02572.hp1 HG02976.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0141a0001c0001t0001g0143 | 2 | 330 | 0.0061 | 11 | c.124 others(28): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
HSF1_chr8_144286604_144319720 | 144313736 | G | GCCTCCCC others(4): Show |
intron_variant | MODIFIER | HG00621.hp1 HG01952.hp1 HG02071.hp2 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0038others(13): Show | 17 | 330 | 0.0515 | 11 | c.124 others(28): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
HSF1_chr8_144286604_144319720 | 144313736 | G | GCGCCGCC others(4): Show |
intron_variant | MODIFIER | HG00558.hp2 HG00609.hp1 HG02145.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0157others(3): Show | 8 | 330 | 0.0242 | 11 | c.124 others(28): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
HSF1_chr8_144286604_144319720 | 144313775 | G | GCCTCCCC others(4): Show |
intron_variant | MODIFIER | HG00140.hp2 HG02818.hp2 HG03139.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0178a0001c0001t0001g0201a0001c0001t0001g0263 | 3 | 330 | 0.0091 | 11 | c.124 others(26): Show |
HSF1 | ENSG00000185122.11 | transcript | ENST00000528838.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
HSF4_chr16_67159745_67174941 | 67167490 | A | AATTTGGG others(4): Show |
frameshift_variant | HIGH | NA19055.hp2 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0001 | 1 | 266 | 0.0038 | 11 | c.747 others(18): Show |
p.Ser others(5): Show |
HSF4 | ENSG00000102878.18 | transcript | ENST00000521374.6 | protein_coding | 8/13 | 825/1702 | 758/1479 | 253/492 | INFO_REALIGN_3_PRIME | chr16 | TogoVar | |
HSF5_chr17_58415167_58493408 | 58433911 | A | ATTTTTTT others(4): Show |
intron_variant | MODIFIER | NA18994.hp2 NA18999.hp2 NA19067.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0180a0001c0001t0001g0215a0002c0002t0001g0225 | 3 | 332 | 0.0090 | 11 | c.172 others(32): Show |
HSF5 | ENSG00000176160.11 | transcript | ENST00000323777.8 | protein_coding | 5/5 | chr17 | TogoVar | ||||||
HSH2D_chr19_16138685_16163575 | 16159722 | C | CAAAAAAA others(4): Show |
downstream_gene_variant | MODIFIER | HG00558.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 | 1 | 394 | 0.0025 | 11 | c.*19 others(22): Show |
HSH2D | ENSG00000196684.12 | transcript | ENST00000613986.4 | protein_coding | 1148 | chr19 | TogoVar | ||||||
HSP90AA1_chr14_102075742_102092044 | 102087280 | T | TCGCACGC others(4): Show |
upstream_gene_variant | MODIFIER | HG00408.hp2 HG02083.hp2 HG02129.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 7 | 398 | 0.0176 | 11 | c.-30 others(20): Show |
HSP90AA1 | ENSG00000080824.19 | transcript | ENST00000216281.13 | protein_coding | 237 | chr14 | TogoVar | ||||||
HSPA12A_chr10_116666192_116747566 | 116696002 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG03471.hp2 NA20129.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0017 | a0001c0001t0002g0147a0001c0001t0017g0258 | 2 | 320 | 0.0063 | 11 | c.546 others(28): Show |
HSPA12A | ENSG00000165868.16 | transcript | ENST00000369209.8 | protein_coding | 5/11 | chr10 | TogoVar | ||||||
HSPA12A_chr10_116666192_116747566 | 116711017 | T | TACAAAGG others(4): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
a0001a0003a0005 | a0001c0001a0001c0002a0001c0006others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(170): Show | 176 | 320 | 0.5500 | 11 | c.41- others(26): Show |
HSPA12A | ENSG00000165868.16 | transcript | ENST00000369209.8 | protein_coding | 1/11 | chr10 | TogoVar | ||||||
HSPA12A_chr10_116666192_116747566 | 116714034 | G | GGGTGGGT others(4): Show |
intron_variant | MODIFIER | HG00735.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(3): Show | a0001c0001t0001g0152a0001c0001t0002g0147a0001c0001t0002g0151others(14): Show | 18 | 320 | 0.0563 | 11 | c.41- others(26): Show |
HSPA12A | ENSG00000165868.16 | transcript | ENST00000369209.8 | protein_coding | 1/11 | chr10 | TogoVar | ||||||
HSPA12B_chr20_3727685_3758111 | 3746301 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | NA19064.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0097 | 1 | 424 | 0.0024 | 11 | c.675 others(26): Show |
HSPA12B | ENSG00000132622.11 | transcript | ENST00000254963.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
HSPA1A_chr6_31810543_31822942 | 31816790 | A | AGCCAGGA others(4): Show |
frameshift_variant | HIGH | NA19062.hp2 | a0005 | a0005c0012 | a0005c0012t0001 | a0005c0012t0001g0000 | 1 | 419 | 0.0024 | 11 | c.103 others(20): Show |
p.Val others(5): Show |
HSPA1A | ENSG00000204389.10 | transcript | ENST00000375651.7 | protein_coding | 1/1 | 1250/2400 | 1036/1926 | 346/641 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |
HSPA1L_chr6_31804619_31820283 | 31809556 | A | ACACACAC others(4): Show |
downstream_gene_variant | MODIFIER | HG02056.hp1 HG06807.hp2 |
a0001a0007 | a0001c0009a0007c0011 | a0001c0009t0001a0007c0011t0001 | a0001c0009t0001g0028a0007c0011t0001g0054 | 2 | 429 | 0.0047 | 11 | c.*49 others(20): Show |
HSPA1L | ENSG00000204390.10 | transcript | ENST00000375654.5 | protein_coding | 62 | chr6 | TogoVar | ||||||
HSPA1L_chr6_31804619_31820283 | 31809595 | A | ACACACAC others(4): Show |
downstream_gene_variant | MODIFIER | HG00642.hp1 HG01517.hp2 HG03669.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0004a0002c0002t0001g0001 | 3 | 429 | 0.0070 | 11 | c.*45 others(20): Show |
HSPA1L | ENSG00000204390.10 | transcript | ENST00000375654.5 | protein_coding | 23 | chr6 | TogoVar | ||||||
HSPA1L_chr6_31804619_31820283 | 31816790 | A | AGCCAGGA others(4): Show |
upstream_gene_variant | MODIFIER | NA19062.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0025 | 1 | 429 | 0.0023 | 11 | c.-19 others(22): Show |
HSPA1L | ENSG00000204390.10 | transcript | ENST00000375654.5 | protein_coding | 1508 | chr6 | TogoVar | ||||||
HSPA4_chr5_133047013_133111449 | 133102913 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG00609.hp2 HG01106.hp1 HG01243.hp2 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(6): Show | a0001c0001t0001g0160a0001c0001t0003g0076a0001c0001t0003g0092others(10): Show | 13 | 364 | 0.0357 | 11 | c.215 others(28): Show |
HSPA4 | ENSG00000170606.16 | transcript | ENST00000304858.7 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
HSPA8_chr11_123052489_123067136 | 123059944 | A | AGATTCCA others(4): Show |
frameshift_variant | HIGH | NA19055.hp1 | a0003 | a0003c0010 | a0003c0010t0003 | a0003c0010t0003g0045 | 1 | 424 | 0.0024 | 11 | c.638 others(18): Show |
p.Phe others(5): Show |
HSPA8 | ENSG00000109971.14 | transcript | ENST00000534624.6 | protein_coding | 5/9 | 726/2264 | 648/1941 | 216/646 | chr11 | TogoVar | ||
HSPB3_chr5_54450699_54461377 | 54451503 | A | AGAGGCAA others(4): Show |
upstream_gene_variant | MODIFIER | HG01433.hp1 HG02486.hp2 HG02818.hp1 others(1): Show |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0000 | 4 | 462 | 0.0087 | 11 | c.-42 others(22): Show |
HSPB3 | ENSG00000169271.3 | transcript | ENST00000302005.3 | protein_coding | 4195 | chr5 | TogoVar | ||||||
HSPG2_chr1_21817244_21942310 | 21863060 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02895.hp2 NA18522.hp1 |
a0014a0066 | a0014c0016a0066c0075 | a0014c0016t0002a0066c0075t0002 | a0014c0016t0002g0058a0066c0075t0002g0166 | 2 | 310 | 0.0065 | 11 | c.474 others(28): Show |
HSPG2 | ENSG00000142798.20 | transcript | ENST00000374695.8 | protein_coding | 37/96 | chr1 | TogoVar | ||||||
HSPG2_chr1_21817244_21942310 | 21870097 | A | AGTCCCCT others(4): Show |
intron_variant | MODIFIER | NA19010.hp1 NA19065.hp2 NA19080.hp1 others(1): Show |
a0001a0074 | a0001c0001a0074c0119 | a0001c0001t0001a0074c0119t0001 | a0001c0001t0001g0008a0001c0001t0001g0291a0074c0119t0001g0297 | 4 | 310 | 0.0129 | 11 | c.422 others(30): Show |
HSPG2 | ENSG00000142798.20 | transcript | ENST00000374695.8 | protein_coding | 33/96 | chr1 | TogoVar | ||||||
HTR1F_chr3_87787706_87998839 | 87869435 | A | AGATAGAT others(4): Show |
intron_variant | MODIFIER | HG00639.hp1 NA19043.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0045a0001c0001t0003g0049 | 2 | 250 | 0.0080 | 11 | c.-43 others(30): Show |
HTR1F | ENSG00000179097.7 | transcript | ENST00000319595.7 | protein_coding | 2/2 | chr3 | TogoVar | ||||||
HTR1F_chr3_87787706_87998839 | 87869439 | A | AGATAGAT others(4): Show |
intron_variant | MODIFIER | HG01255.hp1 HG02257.hp1 HG03041.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003 | a0001c0001t0002g0032a0001c0001t0002g0109a0001c0001t0002g0112others(4): Show | 7 | 250 | 0.0280 | 11 | c.-43 others(30): Show |
HTR1F | ENSG00000179097.7 | transcript | ENST00000319595.7 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
HTR2A_chr13_46826546_46902053 | 46876404 | A | ATATATAT others(4): Show |
intron_variant | MODIFIER | NA18946.hp2 NA18998.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0091a0001c0001t0002g0092 | 2 | 336 | 0.0060 | 11 | c.613 others(30): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | TogoVar | ||||||
HTR2A_chr13_46826546_46902053 | 46876405 | T | TATATATA others(4): Show |
intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0080 | 1 | 336 | 0.0030 | 11 | c.613 others(30): Show |
HTR2A | ENSG00000102468.11 | transcript | ENST00000542664.4 | protein_coding | 3/3 | chr13 | TogoVar | ||||||
HTR2C_chrX_114579086_114915061 | 114616585 | C | CCATCTGT others(4): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(29): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(7): Show | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0016others(29): Show | 32 | 176 | 0.1818 | 11 | c.-80 others(28): Show |
HTR2C | ENSG00000147246.10 | transcript | ENST00000276198.6 | protein_coding | 2/5 | chrX | TogoVar | ||||||
HTR2C_chrX_114579086_114915061 | 114641055 | T | TCTTTTCT others(4): Show |
intron_variant | MODIFIER | HG01167.hp1 HG02257.hp1 HG02486.hp1 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0008a0002c0002t0002g0009a0002c0002t0002g0010others(1): Show | 4 | 176 | 0.0227 | 11 | c.-80 others(30): Show |
HTR2C | ENSG00000147246.10 | transcript | ENST00000276198.6 | protein_coding | 2/5 | chrX | TogoVar | ||||||
HTR2C_chrX_114579086_114915061 | 114734564 | T | TAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG01109.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0058 | 1 | 176 | 0.0057 | 11 | c.349 others(28): Show |
HTR2C | ENSG00000147246.10 | transcript | ENST00000276198.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
HTR2C_chrX_114579086_114915061 | 114741524 | T | TAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG03239.hp2 HG03942.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0100a0001c0001t0001g0165 | 2 | 176 | 0.0114 | 11 | c.349 others(28): Show |
HTR2C | ENSG00000147246.10 | transcript | ENST00000276198.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
HTR2C_chrX_114579086_114915061 | 114764924 | T | TTTCTTTC others(4): Show |
intron_variant | MODIFIER | HG02257.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0009 | 1 | 176 | 0.0057 | 11 | c.349 others(30): Show |
HTR2C | ENSG00000147246.10 | transcript | ENST00000276198.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
HTR2C_chrX_114579086_114915061 | 114805860 | A | ATATACCA others(4): Show |
intron_variant | MODIFIER | HG02572.hp1 HG02615.hp2 HG02886.hp1 others(6): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002a0002c0002t0004 | a0001c0001t0001g0144a0002c0002t0002g0012a0002c0002t0002g0013others(6): Show | 9 | 176 | 0.0511 | 11 | c.350 others(30): Show |
HTR2C | ENSG00000147246.10 | transcript | ENST00000276198.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
HTR2C_chrX_114579086_114915061 | 114806064 | C | CACCATAT others(4): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(123): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0059others(123): Show | 126 | 176 | 0.7159 | 11 | c.350 others(30): Show |
HTR2C | ENSG00000147246.10 | transcript | ENST00000276198.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
HTR2C_chrX_114579086_114915061 | 114807196 | A | ATATACAC others(4): Show |
intron_variant | MODIFIER | HG00639.hp1 HG01106.hp1 HG02559.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0143others(3): Show | 6 | 176 | 0.0341 | 11 | c.350 others(30): Show |
HTR2C | ENSG00000147246.10 | transcript | ENST00000276198.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
HTR2C_chrX_114579086_114915061 | 114807196 | A | ATATATAC others(4): Show |
intron_variant | MODIFIER | HG02615.hp2 NA19030.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0002 | a0001c0001t0001g0144a0002c0002t0002g0015 | 2 | 176 | 0.0114 | 11 | c.350 others(30): Show |
HTR2C | ENSG00000147246.10 | transcript | ENST00000276198.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
HTR2C_chrX_114579086_114915061 | 114807200 | A | ATACCATG others(4): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(44): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(7): Show | a0001c0001t0001g0066a0001c0001t0001g0070a0001c0001t0001g0074others(44): Show | 47 | 176 | 0.2671 | 11 | c.350 others(30): Show |
HTR2C | ENSG00000147246.10 | transcript | ENST00000276198.6 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
HTR2C_chrX_114579086_114915061 | 114894075 | A | ATGGGACT others(4): Show |
intron_variant | MODIFIER | HG02896.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0056 | 1 | 176 | 0.0057 | 11 | c.551 others(30): Show |
HTR2C | ENSG00000147246.10 | transcript | ENST00000276198.6 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
HTR3B_chr11_113899796_113954079 | 113913350 | A | ATTTTTTT others(4): Show |
intron_variant | MODIFIER | HG00423.hp1 HG01496.hp2 HG01981.hp1 others(2): Show |
a0002 | a0002c0002 | a0002c0002t0006 | a0002c0002t0006g0173a0002c0002t0006g0174a0002c0002t0006g0175others(2): Show | 5 | 418 | 0.0120 | 11 | c.213 others(28): Show |
HTR3B | ENSG00000149305.8 | transcript | ENST00000260191.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
HTR3C_chr3_184048047_184065673 | 184055884 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG00597.hp1 HG01192.hp1 HG03688.hp2 others(4): Show |
a0002a0003 | a0002c0002a0003c0003 | a0002c0002t0001a0003c0003t0001 | a0002c0002t0001g0032a0003c0003t0001g0022a0003c0003t0001g0104 | 7 | 442 | 0.0158 | 11 | c.280 others(26): Show |
HTR3C | ENSG00000178084.2 | transcript | ENST00000318351.2 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
HTR3C_chr3_184048047_184065673 | 184065521 | C | CTTTTTTT others(4): Show |
downstream_gene_variant | MODIFIER | HG00621.hp2 HG01346.hp1 HG01346.hp2 others(22): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0001a0001c0001t0004a0002c0002t0001others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(11): Show | 25 | 442 | 0.0566 | 11 | c.*51 others(22): Show |
HTR3C | ENSG00000178084.2 | transcript | ENST00000318351.2 | protein_coding | 4849 | chr3 | TogoVar | ||||||
HTR3E_chr3_184092064_184111995 | 184099739 | A | AAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG01891.hp1 HG03579.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0031 | 2 | 422 | 0.0047 | 11 | c.68- others(24): Show |
HTR3E | ENSG00000186038.9 | transcript | ENST00000415389.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
HTR3E_chr3_184092064_184111995 | 184109324 | C | CAAAAAAA others(4): Show |
downstream_gene_variant | MODIFIER | HG02895.hp2 | a0017 | a0017c0016 | a0017c0016t0001 | a0017c0016t0001g0070 | 1 | 422 | 0.0024 | 11 | c.*26 others(22): Show |
HTR3E | ENSG00000186038.9 | transcript | ENST00000415389.6 | protein_coding | 2330 | chr3 | TogoVar | ||||||
HTR4_chr5_148476547_148659527 | 148576110 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02145.hp1 NA19082.hp2 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0006 | a0001c0001t0003g0095a0001c0001t0006g0203 | 2 | 310 | 0.0065 | 11 | c.27- others(28): Show |
HTR4 | ENSG00000164270.19 | transcript | ENST00000377888.8 | protein_coding | 2/6 | chr5 | TogoVar |