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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
FAM117B_chr2_202629969_202774757 | 202655707 | TGAGAGAG others(9): Show |
T | intron_variant | MODIFIER | HG03098.hp2 HG03471.hp1 HG03831.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0055a0002c0002t0097a0002c0002t0098 | a0001c0001t0055g0161a0002c0002t0097g0315a0002c0002t0098g0316 | 3 | 318 | 0.0094 | -16 | c.601 others(35): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
FAM117B_chr2_202629969_202774757 | 202741416 | CAAAAAAA others(9): Show |
C | intron_variant | MODIFIER | HG00642.hp1 | a0001 | a0001c0001 | a0001c0001t0137 | a0001c0001t0137g0032 | 1 | 318 | 0.0031 | -16 | c.961 others(35): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
FAM117B_chr2_202629969_202774757 | 202746948 | GAAAAAAA others(9): Show |
G | intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0007 | a0001c0007t0106 | a0001c0007t0106g0286 | 1 | 318 | 0.0031 | -16 | c.961 others(33): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
FAM117B_chr2_202629969_202774757 | 202746957 | ACAAAACA others(9): Show |
A | intron_variant | MODIFIER | HG02109.hp1 | a0001 | a0001c0001 | a0001c0001t0101 | a0001c0001t0101g0287 | 1 | 318 | 0.0031 | -16 | c.961 others(33): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 4/7 | chr2 | TogoVar | ||||||
FAM117B_chr2_202629969_202774757 | 202766061 | AACACACA others(9): Show |
A | 3_prime_UTR_variant | MODIFIER | NA18969.hp1 | a0001 | a0001c0001 | a0001c0001t0125 | a0001c0001t0125g0079 | 1 | 318 | 0.0031 | -16 | c.*32 others(25): Show |
FAM117B | ENSG00000138439.12 | transcript | ENST00000392238.3 | protein_coding | 8/8 | 328 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||
FAM118A_chr22_45304934_45346955 | 45323041 | CTGTGTGT others(9): Show |
C | intron_variant | MODIFIER | HG01978.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0063 | 1 | 416 | 0.0024 | -16 | c.48- others(28): Show |
FAM118A | ENSG00000100376.12 | transcript | ENST00000441876.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
FAM118B_chr11_126206782_126267968 | 126214498 | TTTTTGTT others(9): Show |
T | intron_variant | MODIFIER | HG02071.hp2 NA18992.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0027a0001c0001t0001g0219 | 2 | 346 | 0.0058 | -16 | c.-77 others(33): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
FAM118B_chr11_126206782_126267968 | 126219349 | CTTTTTTT others(9): Show |
C | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp2 HG00733.hp1 others(67): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0009a0001c0001t0001g0164a0001c0001t0001g0165others(66): Show | 70 | 346 | 0.2023 | -16 | c.-77 others(33): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
FAM120A_chr9_93446685_93571112 | 93554120 | TACACACA others(9): Show |
T | intron_variant | MODIFIER | HG01123.hp1 HG01358.hp2 HG02109.hp1 others(14): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0001t0006a0001c0001t0016others(3): Show | a0001c0001t0002g0273a0001c0001t0002g0310a0001c0001t0002g0311others(14): Show | 17 | 318 | 0.0535 | -16 | c.227 others(35): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
FAM124A_chr13_51217398_51289239 | 51225976 | CTTTTTTT others(9): Show |
C | intron_variant | MODIFIER | HG00544.hp1 HG00558.hp1 HG03209.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0009a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(4): Show | a0001c0001t0001g0237a0001c0001t0002g0235a0001c0001t0004g0233others(4): Show | 7 | 406 | 0.0172 | -16 | c.68+ others(31): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | |||||
FAM124A_chr13_51217398_51289239 | 51274860 | AGTGAAGA others(9): Show |
A | intron_variant | MODIFIER | NA18997.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0118 | 1 | 406 | 0.0025 | -16 | c.835 others(33): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | TogoVar | ||||||
FAM131C_chr1_16052769_16078651 | 16075333 | CAAAAAAA others(9): Show |
C | upstream_gene_variant | MODIFIER | HG03831.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0082 | 1 | 376 | 0.0027 | -16 | c.-19 others(27): Show |
FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 1683 | chr1 | TogoVar | ||||||
FAM133A_chrX_93669206_93717265 | 93702837 | TAAAAAAA others(9): Show |
T | intron_variant | MODIFIER | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0014 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0180others(6): Show | 11 | 298 | 0.0369 | -16 | c.-10 others(35): Show |
FAM133A | ENSG00000179083.7 | transcript | ENST00000683942.1 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
FAM133B_chr7_92555758_92595390 | 92581794 | TTGTGTGT others(9): Show |
T | intron_variant | MODIFIER | HG02970.hp2 HG03209.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | 328 | 0.0061 | -16 | c.25- others(29): Show |
FAM133B | ENSG00000234545.8 | transcript | ENST00000445716.6 | protein_coding | 1/10 | chr7 | TogoVar | ||||||
FAM135A_chr6_70408508_70566174 | 70450716 | GTTTTTTT others(9): Show |
G | intron_variant | MODIFIER | NA18962.hp1 NA19070.hp2 NA19083.hp1 |
a0001a0002 | a0001c0002a0002c0003 | a0001c0002t0002a0002c0003t0001 | a0001c0002t0002g0168a0002c0003t0001g0116a0002c0003t0001g0117 | 3 | 268 | 0.0112 | -16 | c.78- others(31): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
FAM135B_chr8_138125023_138502261 | 138197103 | GTGTGTGT others(9): Show |
G | intron_variant | MODIFIER | HG02559.hp1 HG02723.hp2 HG02976.hp2 |
a0003 | a0003c0001 | a0003c0001t0004a0003c0001t0006a0003c0001t0031 | a0003c0001t0004g0020a0003c0001t0006g0174a0003c0001t0031g0126 | 3 | 212 | 0.0142 | -16 | c.823 others(31): Show |
FAM135B | ENSG00000147724.12 | transcript | ENST00000395297.6 | protein_coding | 8/19 | chr8 | TogoVar | ||||||
FAM135B_chr8_138125023_138502261 | 138197105 | GTGTGTGT others(9): Show |
G | intron_variant | MODIFIER | HG02965.hp1 HG03486.hp2 HG03834.hp2 others(1): Show |
a0001a0002a0003 | a0001c0006a0002c0002a0003c0001 | a0001c0006t0002a0002c0002t0001a0003c0001t0004others(1): Show | a0001c0006t0002g0183a0002c0002t0001g0039a0003c0001t0004g0002others(1): Show | 4 | 212 | 0.0189 | -16 | c.823 others(31): Show |
FAM135B | ENSG00000147724.12 | transcript | ENST00000395297.6 | protein_coding | 8/19 | chr8 | TogoVar | ||||||
FAM135B_chr8_138125023_138502261 | 138218789 | AGAGAGAG others(9): Show |
A | intron_variant | MODIFIER | HG00423.hp2 HG00639.hp2 HG00741.hp2 others(23): Show |
a0001a0002a0003others(2): Show | a0001c0003a0001c0004a0001c0006others(5): Show | a0001c0003t0003a0001c0003t0018a0001c0004t0001others(10): Show | a0001c0003t0003g0016a0001c0003t0003g0067a0001c0003t0003g0085others(23): Show | 26 | 212 | 0.1226 | -16 | c.670 others(35): Show |
FAM135B | ENSG00000147724.12 | transcript | ENST00000395297.6 | protein_coding | 7/19 | chr8 | TogoVar | ||||||
FAM135B_chr8_138125023_138502261 | 138218796 | GAGAGAGA others(9): Show |
G | intron_variant | MODIFIER | HG02135.hp1 NA20300.hp1 |
a0001 | a0001c0003a0001c0007 | a0001c0003t0003a0001c0007t0004 | a0001c0003t0003g0033a0001c0007t0004g0068 | 2 | 212 | 0.0094 | -16 | c.670 others(35): Show |
FAM135B | ENSG00000147724.12 | transcript | ENST00000395297.6 | protein_coding | 7/19 | chr8 | TogoVar | ||||||
FAM135B_chr8_138125023_138502261 | 138242165 | TTGTGTGT others(9): Show |
T | intron_variant | MODIFIER | HG02559.hp1 HG02723.hp2 HG03579.hp2 |
a0003 | a0003c0001 | a0003c0001t0004a0003c0001t0006a0003c0001t0027 | a0003c0001t0004g0020a0003c0001t0006g0174a0003c0001t0027g0115 | 3 | 212 | 0.0142 | -16 | c.669 others(31): Show |
FAM135B | ENSG00000147724.12 | transcript | ENST00000395297.6 | protein_coding | 7/19 | chr8 | TogoVar | ||||||
FAM135B_chr8_138125023_138502261 | 138394689 | TCTCTCGA others(9): Show |
T | intron_variant | MODIFIER | HG02145.hp1 HG02647.hp1 HG03579.hp2 |
a0001a0003 | a0001c0003a0001c0006a0003c0001 | a0001c0003t0003a0001c0006t0011a0003c0001t0027 | a0001c0003t0003g0074a0001c0006t0011g0117a0003c0001t0027g0115 | 3 | 212 | 0.0142 | -16 | c.-19 others(35): Show |
FAM135B | ENSG00000147724.12 | transcript | ENST00000395297.6 | protein_coding | 1/19 | chr8 | TogoVar | ||||||
FAM135B_chr8_138125023_138502261 | 138425964 | CATATATA others(9): Show |
C | intron_variant | MODIFIER | HG01981.hp1 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0101 | 1 | 212 | 0.0047 | -16 | c.-19 others(35): Show |
FAM135B | ENSG00000147724.12 | transcript | ENST00000395297.6 | protein_coding | 1/19 | chr8 | TogoVar | ||||||
FAM136A_chr2_70290976_70307067 | 70291014 | AACACACA others(9): Show |
A | downstream_gene_variant | MODIFIER | HG00323.hp2 HG02738.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0001 | a0001c0001t0002g0006a0002c0002t0001g0002 | 2 | 440 | 0.0046 | -16 | c.*62 others(27): Show |
FAM136A | ENSG00000035141.10 | transcript | ENST00000430566.6 | protein_coding | 4961 | chr2 | TogoVar | ||||||
FAM13A_chr4_88720960_89062185 | 88961347 | CTTTTTTT others(9): Show |
C | intron_variant | MODIFIER | HG00323.hp1 HG00639.hp1 HG01074.hp1 others(54): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0005others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0037others(54): Show | 57 | 208 | 0.2740 | -16 | c.606 others(35): Show |
FAM13A | ENSG00000138640.15 | transcript | ENST00000264344.10 | protein_coding | 4/23 | chr4 | TogoVar | ||||||
FAM13A_chr4_88720960_89062185 | 89061579 | GTTTTTTT others(9): Show |
G | upstream_gene_variant | MODIFIER | HG01069.hp2 HG01106.hp1 HG01167.hp1 others(20): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0011others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0003t0004others(5): Show | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(20): Show | 23 | 208 | 0.1106 | -16 | c.-46 others(27): Show |
FAM13A | ENSG00000138640.15 | transcript | ENST00000264344.10 | protein_coding | 4395 | chr4 | TogoVar | ||||||
FAM13B_chr5_137932960_138038079 | 137966480 | TATATATA others(9): Show |
T | intron_variant | MODIFIER | HG02280.hp2 HG06807.hp1 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0258a0001c0001t0004g0264 | 2 | 322 | 0.0062 | -16 | c.118 others(35): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | TogoVar | ||||||
FAM13B_chr5_137932960_138038079 | 137966482 | TATATATA others(9): Show |
T | intron_variant | MODIFIER | HG02717.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0260 | 1 | 322 | 0.0031 | -16 | c.118 others(35): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | TogoVar | ||||||
FAM13B_chr5_137932960_138038079 | 137983176 | TAAAAAAA others(9): Show |
T | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(120): Show |
a0001a0003a0004 | a0001c0001a0001c0004a0003c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(120): Show | 123 | 322 | 0.3820 | -16 | c.117 others(35): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | TogoVar | ||||||
FAM13B_chr5_137932960_138038079 | 138026938 | CAAATAAA others(9): Show |
C | intron_variant | MODIFIER | HG01070.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0074 | 1 | 322 | 0.0031 | -16 | c.-20 others(35): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1/23 | chr5 | TogoVar | ||||||
FAM13C_chr10_59241133_59367549 | 59319072 | AACACACA others(9): Show |
A | intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0091 | 1 | 204 | 0.0049 | -16 | c.443 others(33): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | TogoVar | ||||||
FAM13C_chr10_59241133_59367549 | 59329582 | CTCCTGAC others(9): Show |
C | intron_variant | MODIFIER | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | 204 | 0.0245 | -16 | c.325 others(33): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | TogoVar | ||||||
FAM149A_chr4_186099704_186180337 | 186136948 | CTCTCTCT others(9): Show |
C | intron_variant | MODIFIER | HG02809.hp2 HG03540.hp1 |
a0002 | a0002c0004a0002c0016 | a0002c0004t0015a0002c0016t0084 | a0002c0004t0015g0383a0002c0016t0084g0384 | 2 | 390 | 0.0051 | -16 | c.567 others(35): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
FAM149A_chr4_186099704_186180337 | 186136960 | CTCTTTCT others(9): Show |
C | intron_variant | MODIFIER | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(11): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0005a0002c0004others(6): Show | a0001c0001t0001a0001c0001t0010a0001c0005t0002others(8): Show | a0001c0001t0001g0077a0001c0001t0010g0377a0001c0005t0002g0043others(11): Show | 14 | 390 | 0.0359 | -16 | c.567 others(35): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
FAM149A_chr4_186099704_186180337 | 186136964 | TTCTCTCT others(9): Show |
T | intron_variant | MODIFIER | HG02165.hp1 HG02257.hp2 HG02615.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0002a0002c0004t0005a0002c0004t0020 | a0001c0001t0002g0084a0001c0001t0002g0123a0002c0004t0005g0165others(2): Show | 5 | 390 | 0.0128 | -16 | c.567 others(35): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
FAM149A_chr4_186099704_186180337 | 186152605 | CGCGATCT others(9): Show |
C | intron_variant | MODIFIER | HG01884.hp2 HG02976.hp2 |
a0005 | a0005c0006 | a0005c0006t0072a0005c0006t0087 | a0005c0006t0072g0295a0005c0006t0087g0374 | 2 | 390 | 0.0051 | -16 | c.959 others(31): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
FAM149A_chr4_186099704_186180337 | 186160201 | ACACACAC others(9): Show |
A | intron_variant | MODIFIER | HG02280.hp2 HG02717.hp2 NA19009.hp2 others(1): Show |
a0001a0006 | a0001c0001a0006c0018 | a0001c0001t0002a0006c0018t0026a0006c0018t0069 | a0001c0001t0002g0082a0006c0018t0026g0266a0006c0018t0026g0269others(1): Show | 4 | 390 | 0.0103 | -16 | c.160 others(35): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
FAM149A_chr4_186099704_186180337 | 186176917 | ATGTGTGT others(9): Show |
A | downstream_gene_variant | MODIFIER | HG00099.hp2 HG01167.hp1 HG01169.hp1 others(2): Show |
a0005a0022 | a0005c0006a0022c0056 | a0005c0006t0007a0022c0056t0057 | a0005c0006t0007g0064a0005c0006t0007g0128a0005c0006t0007g0129others(2): Show | 5 | 390 | 0.0128 | -16 | c.*49 others(27): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 1581 | chr4 | TogoVar | ||||||
FAM149B1_chr10_73163119_73249504 | 73188756 | GGGAAGGA others(9): Show |
G | intron_variant | MODIFIER | NA18953.hp2 NA18970.hp2 NA18993.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0100a0001c0001t0001g0182a0001c0001t0001g0189 | 3 | 236 | 0.0127 | -16 | c.283 others(33): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
FAM149B1_chr10_73163119_73249504 | 73204944 | ATTTTTTT others(9): Show |
A | intron_variant | MODIFIER | HG01069.hp2 HG03471.hp1 HG06807.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0015a0001c0001t0021 | a0001c0001t0001g0208a0001c0001t0015g0214a0001c0001t0021g0192 | 3 | 236 | 0.0127 | -16 | c.543 others(33): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
FAM151B_chr5_80483100_80547563 | 80494456 | TTTTCTTT others(9): Show |
T | intron_variant | MODIFIER | HG00323.hp1 HG03654.hp1 NA18906.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0305a0001c0001t0001g0342a0001c0001t0001g0343 | 3 | 356 | 0.0084 | -16 | c.25+ others(31): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
FAM151B_chr5_80483100_80547563 | 80521116 | CTTTTTTT others(9): Show |
C | intron_variant | MODIFIER | HG02717.hp1 HG02895.hp1 HG02896.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0228a0001c0001t0001g0231a0001c0001t0001g0233others(1): Show | 4 | 356 | 0.0112 | -16 | c.536 others(31): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
FAM151B_chr5_80483100_80547563 | 80538372 | TTTTCTTT others(9): Show |
T | intron_variant | MODIFIER | NA20905.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0114 | 1 | 356 | 0.0028 | -16 | c.672 others(33): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
FAM151B_chr5_80483100_80547563 | 80538436 | CTTTCTTT others(9): Show |
C | intron_variant | MODIFIER | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0065others(5): Show | 8 | 356 | 0.0225 | -16 | c.672 others(33): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
FAM151B_chr5_80483100_80547563 | 80538440 | CTTTCTTT others(9): Show |
C | intron_variant | MODIFIER | NA20752.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0328 | 1 | 356 | 0.0028 | -16 | c.672 others(33): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
FAM151B_chr5_80483100_80547563 | 80538444 | CTTTCTCT others(9): Show |
C | intron_variant | MODIFIER | HG02109.hp2 HG02735.hp1 HG02965.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0019a0001c0001t0001g0106a0001c0001t0001g0164others(1): Show | 4 | 356 | 0.0112 | -16 | c.672 others(33): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
FAM151B_chr5_80483100_80547563 | 80538509 | TTTCTTTC others(9): Show |
T | intron_variant | MODIFIER | HG02922.hp2 HG03516.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0300a0001c0001t0001g0308 | 2 | 356 | 0.0056 | -16 | c.672 others(33): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
FAM151B_chr5_80483100_80547563 | 80538513 | TTTCCTTC others(9): Show |
T | intron_variant | MODIFIER | HG00323.hp1 HG00438.hp2 HG01496.hp2 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0077a0001c0001t0001g0302a0001c0001t0001g0305others(8): Show | 11 | 356 | 0.0309 | -16 | c.672 others(33): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
FAM161B_chr14_73927276_73955094 | 73934979 | GGAGACTG others(9): Show |
G | intron_variant | MODIFIER | NA18969.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0084 | 1 | 442 | 0.0023 | -16 | c.180 others(33): Show |
FAM161B | ENSG00000156050.10 | transcript | ENST00000286544.5 | protein_coding | 8/8 | chr14 | TogoVar | ||||||
FAM162A_chr3_122379182_122417334 | 122389381 | GGATAGAT others(9): Show |
G | intron_variant | MODIFIER | HG00639.hp2 HG01081.hp2 HG01167.hp2 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0130others(4): Show | 16 | 422 | 0.0379 | -16 | c.34+ others(31): Show |
FAM162A | ENSG00000114023.16 | transcript | ENST00000477892.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
FAM162B_chr6_116747197_116770719 | 116749272 | GCTATCGT others(9): Show |
G | downstream_gene_variant | MODIFIER | NA19059.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0034 | 1 | 474 | 0.0021 | -16 | c.*33 others(27): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 2924 | chr6 | TogoVar |