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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
FAM118B_chr11_126206782_126267968 | 126249743 | AAAAAAAA others(11): Show |
A | intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0170 | 1 | 346 | 0.0029 | -18 | c.340 others(33): Show |
FAM118B | ENSG00000197798.9 | transcript | ENST00000533050.6 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
FAM120A_chr9_93446685_93571112 | 93554120 | TACACACA others(11): Show |
T | intron_variant | MODIFIER | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(8): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0002 | a0001c0002t0001g0206a0001c0003t0002g0005a0001c0003t0002g0006others(8): Show | 11 | 318 | 0.0346 | -18 | c.227 others(37): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
FAM120A_chr9_93446685_93571112 | 93561760 | CATTAAAT others(11): Show |
C | intron_variant | MODIFIER | HG02896.hp1 HG02897.hp2 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0197a0001c0002t0001g0202 | 2 | 318 | 0.0063 | -18 | c.294 others(35): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | |||||
FAM120B_chr6_170301758_170412067 | 170361198 | GTATATAT others(11): Show |
G | intron_variant | MODIFIER | HG02015.hp1 HG02129.hp1 NA18939.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0194a0001c0001t0008g0195a0001c0001t0008g0197others(2): Show | 5 | 289 | 0.0173 | -18 | c.228 others(37): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
FAM120B_chr6_170301758_170412067 | 170361219 | TATATATA others(11): Show |
T | intron_variant | MODIFIER | NA18990.hp2 | a0002 | a0002c0003 | a0002c0003t0002 | a0002c0003t0002g0115 | 1 | 289 | 0.0035 | -18 | c.228 others(37): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
FAM124A_chr13_51217398_51289239 | 51288443 | TCTCCTCC others(11): Show |
T | downstream_gene_variant | MODIFIER | HG00099.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0332 | 1 | 406 | 0.0025 | -18 | c.*71 others(29): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4205 | chr13 | TogoVar | ||||||
FAM124A_chr13_51217398_51289239 | 51288544 | CCTCCTCC others(11): Show |
C | downstream_gene_variant | MODIFIER | HG01167.hp2 HG01169.hp1 HG02080.hp1 others(6): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0014 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(4): Show | a0001c0001t0001g0010a0001c0001t0002g0130a0001c0001t0005g0082others(6): Show | 9 | 406 | 0.0222 | -18 | c.*72 others(29): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4306 | chr13 | TogoVar | ||||||
FAM133A_chrX_93669206_93717265 | 93679915 | ATTTTTTT others(11): Show |
A | intron_variant | MODIFIER | HG02896.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0029 | 1 | 298 | 0.0034 | -18 | c.-19 others(37): Show |
FAM133A | ENSG00000179083.7 | transcript | ENST00000683942.1 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
FAM135A_chr6_70408508_70566174 | 70450716 | GTTTTTTT others(11): Show |
G | intron_variant | MODIFIER | HG00280.hp1 HG00597.hp1 HG00609.hp1 others(53): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0016 | a0001c0001t0001a0001c0002t0002a0002c0016t0002 | a0001c0001t0001g0210a0001c0002t0002g0167a0001c0002t0002g0173others(53): Show | 56 | 268 | 0.2090 | -18 | c.78- others(33): Show |
FAM135A | ENSG00000082269.17 | transcript | ENST00000418814.7 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
FAM135B_chr8_138125023_138502261 | 138197101 | GTGTGTGT others(11): Show |
G | intron_variant | MODIFIER | HG02145.hp1 HG02451.hp1 HG02615.hp2 others(4): Show |
a0001a0002a0003 | a0001c0004a0001c0005a0001c0006others(3): Show | a0001c0004t0002a0001c0005t0001a0001c0005t0002others(4): Show | a0001c0004t0002g0156a0001c0005t0001g0090a0001c0005t0002g0151others(4): Show | 7 | 212 | 0.0330 | -18 | c.823 others(33): Show |
FAM135B | ENSG00000147724.12 | transcript | ENST00000395297.6 | protein_coding | 8/19 | chr8 | TogoVar | ||||||
FAM135B_chr8_138125023_138502261 | 138197103 | GTGTGTGT others(11): Show |
G | intron_variant | MODIFIER | HG01975.hp2 HG03195.hp1 |
a0001a0003 | a0001c0013a0003c0001 | a0001c0013t0002a0003c0001t0006 | a0001c0013t0002g0137a0003c0001t0006g0162 | 2 | 212 | 0.0094 | -18 | c.823 others(33): Show |
FAM135B | ENSG00000147724.12 | transcript | ENST00000395297.6 | protein_coding | 8/19 | chr8 | TogoVar | ||||||
FAM135B_chr8_138125023_138502261 | 138214439 | ATTTGTGT others(11): Show |
A | intron_variant | MODIFIER | HG02615.hp2 HG03098.hp2 NA19240.hp1 |
a0001a0003 | a0001c0005a0003c0001 | a0001c0005t0001a0001c0005t0002a0003c0001t0009 | a0001c0005t0001g0090a0001c0005t0002g0151a0003c0001t0009g0180 | 3 | 212 | 0.0142 | -18 | c.670 others(37): Show |
FAM135B | ENSG00000147724.12 | transcript | ENST00000395297.6 | protein_coding | 7/19 | chr8 | TogoVar | ||||||
FAM135B_chr8_138125023_138502261 | 138218787 | AGAGAGAG others(11): Show |
A | intron_variant | MODIFIER | HG02257.hp2 | a0008 | a0008c0016 | a0008c0016t0008 | a0008c0016t0008g0127 | 1 | 212 | 0.0047 | -18 | c.670 others(37): Show |
FAM135B | ENSG00000147724.12 | transcript | ENST00000395297.6 | protein_coding | 7/19 | chr8 | TogoVar | ||||||
FAM135B_chr8_138125023_138502261 | 138425964 | CATATATA others(11): Show |
C | intron_variant | MODIFIER | HG01099.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0105 | 1 | 212 | 0.0047 | -18 | c.-19 others(37): Show |
FAM135B | ENSG00000147724.12 | transcript | ENST00000395297.6 | protein_coding | 1/19 | chr8 | TogoVar | ||||||
FAM13A_chr4_88720960_89062185 | 88945990 | GTATATAT others(11): Show |
G | intron_variant | MODIFIER | HG00323.hp2 HG01069.hp2 HG01106.hp1 others(16): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0011others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0003t0004others(4): Show | a0001c0001t0001g0013a0001c0001t0001g0022a0001c0001t0001g0026others(16): Show | 19 | 208 | 0.0914 | -18 | c.606 others(35): Show |
FAM13A | ENSG00000138640.15 | transcript | ENST00000264344.10 | protein_coding | 4/23 | chr4 | TogoVar | ||||||
FAM13A_chr4_88720960_89062185 | 88961347 | CTTTTTTT others(11): Show |
C | intron_variant | MODIFIER | HG03942.hp2 | a0001 | a0001c0003 | a0001c0003t0007 | a0001c0003t0007g0019 | 1 | 208 | 0.0048 | -18 | c.606 others(37): Show |
FAM13A | ENSG00000138640.15 | transcript | ENST00000264344.10 | protein_coding | 4/23 | chr4 | TogoVar | ||||||
FAM13B_chr5_137932960_138038079 | 137966474 | TATATATA others(11): Show |
T | intron_variant | MODIFIER | HG02970.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0261 | 1 | 322 | 0.0031 | -18 | c.118 others(37): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | TogoVar | ||||||
FAM13B_chr5_137932960_138038079 | 137966476 | TATATATA others(11): Show |
T | intron_variant | MODIFIER | HG02896.hp2 HG02897.hp1 NA18906.hp2 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0006 | a0001c0001t0004g0265a0001c0001t0006g0262a0001c0001t0006g0263 | 3 | 322 | 0.0093 | -18 | c.118 others(37): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | TogoVar | ||||||
FAM13B_chr5_137932960_138038079 | 137966482 | TATATATA others(11): Show |
T | intron_variant | MODIFIER | HG02145.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0259 | 1 | 322 | 0.0031 | -18 | c.118 others(37): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | TogoVar | ||||||
FAM13B_chr5_137932960_138038079 | 138034995 | CTTTTTTT others(11): Show |
C | upstream_gene_variant | MODIFIER | HG01243.hp2 HG03098.hp2 HG03540.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0257 | 3 | 322 | 0.0093 | -18 | c.-24 others(29): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1917 | chr5 | TogoVar | ||||||
FAM13C_chr10_59241133_59367549 | 59319103 | ACACACAC others(11): Show |
A | intron_variant | MODIFIER | HG01167.hp1 HG01891.hp1 HG02622.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0178a0001c0001t0001g0200a0001c0001t0001g0201others(2): Show | 5 | 204 | 0.0245 | -18 | c.443 others(35): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | TogoVar | ||||||
FAM13C_chr10_59241133_59367549 | 59329342 | GTTTTTTT others(11): Show |
G | intron_variant | MODIFIER | NA19090.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0073 | 1 | 204 | 0.0049 | -18 | c.325 others(35): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 3/13 | chr10 | TogoVar | ||||||
FAM149A_chr4_186099704_186180337 | 186136946 | CTCTCTCT others(11): Show |
C | intron_variant | MODIFIER | HG02486.hp1 HG06807.hp2 NA19011.hp2 others(1): Show |
a0004a0005 | a0004c0003a0005c0006 | a0004c0003t0003a0004c0003t0005a0005c0006t0017 | a0004c0003t0003g0177a0004c0003t0005g0222a0005c0006t0017g0158others(1): Show | 4 | 390 | 0.0103 | -18 | c.567 others(37): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
FAM149A_chr4_186099704_186180337 | 186136964 | TTCTCTCT others(11): Show |
T | intron_variant | MODIFIER | HG02280.hp2 HG02717.hp2 |
a0006 | a0006c0018 | a0006c0018t0026a0006c0018t0069 | a0006c0018t0026g0266a0006c0018t0069g0265 | 2 | 390 | 0.0051 | -18 | c.567 others(37): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
FAM149A_chr4_186099704_186180337 | 186144924 | GGCGGGCG others(11): Show |
G | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
a0001a0002a0003others(17): Show | a0001c0001a0001c0010a0001c0014others(26): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(65): Show | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(171): Show | 175 | 390 | 0.4487 | -18 | 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 | 186160275 | AACACACC others(11): Show |
A | intron_variant | MODIFIER | NA19009.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0313 | 1 | 390 | 0.0026 | -18 | c.160 others(37): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
FAM149B1_chr10_73163119_73249504 | 73204944 | ATTTTTTT others(11): Show |
A | intron_variant | MODIFIER | HG00735.hp2 HG02257.hp2 HG02717.hp2 others(2): Show |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0001a0001c0001t0004a0003c0003t0001others(1): Show | a0001c0001t0001g0117a0001c0001t0001g0157a0001c0001t0004g0194others(2): Show | 5 | 236 | 0.0212 | -18 | c.543 others(35): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
FAM151B_chr5_80483100_80547563 | 80517484 | TCAAGTTT others(11): Show |
T | intron_variant | MODIFIER | NA19056.hp1 NA19075.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0071a0001c0001t0001g0129 | 2 | 356 | 0.0056 | -18 | c.318 others(35): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 3/5 | chr5 | TogoVar | ||||||
FAM161A_chr2_61819848_61859060 | 61848890 | ATATATTT others(11): Show |
A | intron_variant | MODIFIER | HG00738.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0016a0002c0002t0002g0219 | 4 | 400 | 0.0100 | -18 | c.183 others(35): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | TogoVar | ||||||
FAM163B_chr9_133572081_133614389 | 133586263 | CCAGCTCA others(11): Show |
C | intron_variant | MODIFIER | NA19002.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0252 | 1 | 382 | 0.0026 | -18 | c.-23 others(35): Show |
FAM163B | ENSG00000196990.10 | transcript | ENST00000673969.1 | protein_coding | 1/2 | chr9 | TogoVar | ||||||
FAM163B_chr9_133572081_133614389 | 133590171 | CCCTTCTT others(11): Show |
C | intron_variant | MODIFIER | HG02145.hp2 HG03139.hp2 HG03209.hp2 others(3): Show |
a0001 | a0001c0001a0001c0011 | a0001c0001t0003a0001c0011t0003 | a0001c0001t0003g0021a0001c0001t0003g0061a0001c0001t0003g0295others(1): Show | 6 | 382 | 0.0157 | -18 | c.-23 others(35): Show |
FAM163B | ENSG00000196990.10 | transcript | ENST00000673969.1 | protein_coding | 1/2 | chr9 | TogoVar | ||||||
FAM167A_chr8_11416476_11471753 | 11422373 | GGTGTGTG others(11): Show |
G | 3_prime_UTR_variant | MODIFIER | HG02647.hp2 HG03579.hp2 NA20129.hp2 |
a0001 | a0001c0001 | a0001c0001t0055a0001c0001t0076a0001c0001t0089 | a0001c0001t0055g0025a0001c0001t0076g0266a0001c0001t0089g0024 | 3 | 374 | 0.0080 | -18 | c.*19 others(29): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1982 | chr8 | TogoVar | |||||
FAM168A_chr11_73395487_73603112 | 73442955 | GATATATA others(11): Show |
G | intron_variant | MODIFIER | HG00323.hp2 | a0001 | a0001c0002 | a0001c0002t0051 | a0001c0002t0051g0108 | 1 | 180 | 0.0056 | -18 | c.71- others(35): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | TogoVar | ||||||
FAM169A_chr5_74772574_74871387 | 74773632 | CCTGTCTC others(11): Show |
C | downstream_gene_variant | MODIFIER | HG00642.hp2 | a0001 | a0001c0001 | a0001c0001t0023 | a0001c0001t0023g0186 | 1 | 308 | 0.0033 | -18 | c.*78 others(29): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 3941 | chr5 | TogoVar | ||||||
FAM171A1_chr10_15206643_15376289 | 15211314 | CTTTTTTT others(11): Show |
C | downstream_gene_variant | MODIFIER | HG02647.hp2 HG03098.hp1 HG03490.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0014a0002c0002 | a0001c0001t0003a0001c0001t0010a0001c0014t0003others(1): Show | a0001c0001t0003g0278a0001c0001t0003g0297a0001c0001t0010g0007others(2): Show | 5 | 303 | 0.0165 | -18 | c.*15 others(29): Show |
FAM171A1 | ENSG00000148468.17 | transcript | ENST00000378116.9 | protein_coding | 328 | chr10 | TogoVar | ||||||
FAM171A2_chr17_44348215_44368853 | 44368138 | ATATATAT others(11): Show |
A | upstream_gene_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023 | 1 | 416 | 0.0024 | -18 | c.-44 others(29): Show |
FAM171A2 | ENSG00000161682.15 | transcript | ENST00000293443.12 | protein_coding | 4286 | chr17 | TogoVar | ||||||
FAM172A_chr5_93612725_94116663 | 93653511 | CAAAAAAA others(11): Show |
C | intron_variant | MODIFIER | HG00099.hp2 HG00733.hp1 HG01070.hp1 others(23): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(23): Show | 26 | 126 | 0.2064 | -18 | c.110 others(39): Show |
FAM172A | ENSG00000113391.19 | transcript | ENST00000395965.8 | protein_coding | 10/10 | chr5 | TogoVar | ||||||
FAM172A_chr5_93612725_94116663 | 93983170 | GGTGTGTG others(11): Show |
G | intron_variant | MODIFIER | HG03516.hp2 NA18970.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0068a0001c0001t0002g0122 | 2 | 126 | 0.0159 | -18 | c.310 others(37): Show |
FAM172A | ENSG00000113391.19 | transcript | ENST00000395965.8 | protein_coding | 4/10 | chr5 | TogoVar | ||||||
FAM174B_chr15_92612448_92660775 | 92618728 | GCACACGC others(11): Show |
G | 3_prime_UTR_variant | MODIFIER | HG02486.hp2 | a0001 | a0001c0001 | a0001c0001t0052 | a0001c0001t0052g0317 | 1 | 394 | 0.0025 | -18 | c.*71 others(27): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 3/3 | 710 | chr15 | TogoVar | |||||
FAM174B_chr15_92612448_92660775 | 92640551 | CAAAAAAA others(11): Show |
C | intron_variant | MODIFIER | HG01891.hp1 HG02055.hp2 HG02572.hp2 others(8): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0003a0001c0001t0009a0001c0001t0059others(1): Show | a0001c0001t0003g0001a0001c0001t0003g0018a0001c0001t0009g0019others(6): Show | 11 | 394 | 0.0279 | -18 | c.345 others(37): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | TogoVar | ||||||
FAM177A1_chr14_35041272_35088378 | 35070114 | CAAAAAAA others(11): Show |
C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(74): Show | 108 | 370 | 0.2919 | -18 | c.340 others(35): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
FAM178B_chr2_96870885_96991580 | 96905814 | GTGTGTAT others(11): Show |
G | intron_variant | MODIFIER | HG02083.hp1 | a0002 | a0002c0008 | a0002c0008t0001 | a0002c0008t0001g0232 | 1 | 250 | 0.0040 | -18 | c.156 others(37): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | TogoVar | ||||||
FAM178B_chr2_96870885_96991580 | 96905852 | ATATATAT others(11): Show |
A | intron_variant | MODIFIER | HG01358.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0044 | 1 | 250 | 0.0040 | -18 | c.156 others(37): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | TogoVar | ||||||
FAM178B_chr2_96870885_96991580 | 96930210 | CAAAAAAA others(11): Show |
C | intron_variant | MODIFIER | NA19074.hp1 NA19074.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0050a0002c0002t0001g0169 | 2 | 250 | 0.0080 | -18 | c.107 others(35): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | TogoVar | ||||||
FAM178B_chr2_96870885_96991580 | 96945284 | CACACTAG others(11): Show |
C | intron_variant | MODIFIER | HG01106.hp2 HG02602.hp2 HG02698.hp2 others(3): Show |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0206a0002c0002t0001g0207a0002c0002t0001g0208others(3): Show | 6 | 250 | 0.0240 | -18 | c.107 others(37): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 8/16 | chr2 | TogoVar | ||||||
FAM178B_chr2_96870885_96991580 | 96987178 | CAAAAAAA others(11): Show |
C | upstream_gene_variant | MODIFIER | HG01891.hp1 | a0014 | a0014c0021 | a0014c0021t0001 | a0014c0021t0001g0225 | 1 | 250 | 0.0040 | -18 | c.-88 others(27): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 599 | chr2 | TogoVar | ||||||
FAM180A_chr7_135724592_135753813 | 135732689 | TCACACAC others(11): Show |
T | intron_variant | MODIFIER | HG01123.hp2 HG01192.hp2 HG01261.hp2 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0006 | a0001c0001t0002g0010a0001c0001t0002g0055a0001c0001t0002g0058others(3): Show | 14 | 436 | 0.0321 | -18 | c.*32 others(35): Show |
FAM180A | ENSG00000189320.9 | transcript | ENST00000338588.8 | protein_coding | 3/3 | chr7 | TogoVar | ||||||
FAM180B_chr11_47581678_47594194 | 47588707 | AGTGTGTG others(11): Show |
A | 3_prime_UTR_variant | MODIFIER | HG02486.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0003a0001c0001t0008g0013 | 11 | 414 | 0.0266 | -18 | c.*28 others(27): Show |
FAM180B | ENSG00000196666.6 | transcript | ENST00000538490.3 | protein_coding | 3/3 | 285 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||
FAM184A_chr6_118954763_119083664 | 119034035 | TATATATA others(11): Show |
T | intron_variant | MODIFIER | HG01168.hp1 HG02895.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0100a0001c0001t0005g0026 | 2 | 286 | 0.0070 | -18 | c.160 others(35): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | TogoVar | ||||||
FAM184A_chr6_118954763_119083664 | 119034041 | TAGAGAGA others(11): Show |
T | intron_variant | MODIFIER | HG01074.hp2 HG01433.hp2 HG01496.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0081a0001c0001t0001g0243a0001c0001t0001g0244others(1): Show | 4 | 286 | 0.0140 | -18 | c.160 others(35): Show |
FAM184A | ENSG00000111879.20 | transcript | ENST00000338891.12 | protein_coding | 1/17 | chr6 | TogoVar |