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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
FAF1_chr1_50432028_50965267 | 50554390 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | NA18957.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0038 | 1 | 190 | 0.0053 | 30 | c.126 others(51): Show |
FAF1 | ENSG00000185104.21 | transcript | ENST00000396153.7 | protein_coding | 13/18 | chr1 | TogoVar | |||||||
FAF1_chr1_50432028_50965267 | 50554390 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | NA20300.hp1 | a0001 | a0001c0001 | a0001c0001t0033 | a0001c0001t0033g0121 | 1 | 190 | 0.0053 | 30 | c.126 others(51): Show |
FAF1 | ENSG00000185104.21 | transcript | ENST00000396153.7 | protein_coding | 13/18 | chr1 | TogoVar | |||||||
FAF1_chr1_50432028_50965267 | 50554390 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | HG01517.hp2 | a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0006 | 1 | 190 | 0.0053 | 30 | c.126 others(51): Show |
FAF1 | ENSG00000185104.21 | transcript | ENST00000396153.7 | protein_coding | 13/18 | chr1 | TogoVar | |||||||
FAF1_chr1_50432028_50965267 | 50554390 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | HG02145.hp1 | a0001 | a0001c0001 | a0001c0001t0036 | a0001c0001t0036g0120 | 1 | 190 | 0.0053 | 30 | c.126 others(51): Show |
FAF1 | ENSG00000185104.21 | transcript | ENST00000396153.7 | protein_coding | 13/18 | chr1 | TogoVar | |||||||
FAF1_chr1_50432028_50965267 | 50819739 | A | ATACGTAT others(23): Show |
intron_variant | MODIFIER | HG00140.hp1 HG01255.hp1 HG01256.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(4): Show | a0001c0001t0001g0145 a0001c0001t0002g0126 a0001c0001t0002g0128 others(10): Show |
13 | 190 | 0.0684 | 30 | c.115 others(49): Show |
FAF1 | ENSG00000185104.21 | transcript | ENST00000396153.7 | protein_coding | 2/18 | chr1 | TogoVar | |||||||
FAF1_chr1_50432028_50965267 | 50885312 | T | TCTCACAC others(23): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0183 | 1 | 190 | 0.0053 | 30 | c.46- others(47): Show |
FAF1 | ENSG00000185104.21 | transcript | ENST00000396153.7 | protein_coding | 1/18 | chr1 | TogoVar | |||||||
FAH_chr15_80147999_80191349 | 80153171 | G | GGGAGTGG others(23): Show |
intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0024 a0001c0001t0001g0204 |
4 | 428 | 0.0094 | 30 | c.81+ others(41): Show |
FAH | ENSG00000103876.14 | transcript | ENST00000561421.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | ||||||
FAM104A_chr17_73202365_73237394 | 73224960 | G | GACAGCAC others(23): Show |
intron_variant | MODIFIER | HG00280.hp2 HG00642.hp2 HG01515.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0020 | a0001c0001t0001g0068 a0001c0001t0001g0355 a0001c0001t0001g0356 others(1): Show |
4 | 400 | 0.0100 | 30 | c.321 others(47): Show |
FAM104A | ENSG00000133193.13 | transcript | ENST00000405159.8 | protein_coding | 2/3 | chr17 | TogoVar | |||||||
FAM104A_chr17_73202365_73237394 | 73224960 | G | GACAGGAC others(23): Show |
intron_variant | MODIFIER | HG02145.hp2 HG02559.hp2 HG02809.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0009a0001c0001t0017 | a0001c0001t0001g0017 a0001c0001t0001g0175 a0001c0001t0001g0177 others(4): Show |
9 | 400 | 0.0225 | 30 | c.321 others(47): Show |
FAM104A | ENSG00000133193.13 | transcript | ENST00000405159.8 | protein_coding | 2/3 | chr17 | TogoVar | |||||||
FAM104A_chr17_73202365_73237394 | 73225899 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG01106.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0205 | 1 | 400 | 0.0025 | 30 | c.321 others(47): Show |
FAM104A | ENSG00000133193.13 | transcript | ENST00000405159.8 | protein_coding | 2/3 | chr17 | TogoVar | |||||||
FAM104A_chr17_73202365_73237394 | 73225900 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | NA19078.hp1 | a0002 | a0002c0005 | a0002c0005t0001 | a0002c0005t0001g0265 | 1 | 400 | 0.0025 | 30 | c.321 others(47): Show |
FAM104A | ENSG00000133193.13 | transcript | ENST00000405159.8 | protein_coding | 2/3 | chr17 | TogoVar | |||||||
FAM104A_chr17_73202365_73237394 | 73234773 | C | CTGTGTGT others(23): Show |
upstream_gene_variant | MODIFIER | HG02083.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 | 1 | 400 | 0.0025 | 30 | c.-24 others(41): Show |
FAM104A | ENSG00000133193.13 | transcript | ENST00000405159.8 | protein_coding | 2380 | chr17 | TogoVar | |||||||
FAM107B_chr10_14513557_14779897 | 14572736 | A | ATTATATA others(23): Show |
intron_variant | MODIFIER | HG03540.hp1 | a0001 | a0001c0001 | a0001c0001t0024 | a0001c0001t0024g0136 | 1 | 272 | 0.0037 | 30 | c.470 others(49): Show |
FAM107B | ENSG00000065809.14 | transcript | ENST00000181796.7 | protein_coding | 2/4 | chr10 | TogoVar | |||||||
FAM107B_chr10_14513557_14779897 | 14572736 | A | ATTTTATA others(23): Show |
intron_variant | MODIFIER | NA20129.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 | 1 | 272 | 0.0037 | 30 | c.470 others(49): Show |
FAM107B | ENSG00000065809.14 | transcript | ENST00000181796.7 | protein_coding | 2/4 | chr10 | TogoVar | |||||||
FAM107B_chr10_14513557_14779897 | 14737766 | T | TTCTCTCT others(23): Show |
intron_variant | MODIFIER | HG00544.hp1 HG02559.hp2 HG03942.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(2): Show | a0001c0001t0001g0037 a0001c0001t0001g0084 a0001c0001t0001g0135 others(4): Show |
7 | 272 | 0.0257 | 30 | c.411 others(49): Show |
FAM107B | ENSG00000065809.14 | transcript | ENST00000181796.7 | protein_coding | 1/4 | chr10 | TogoVar | |||||||
FAM107B_chr10_14513557_14779897 | 14767024 | G | GTATATAT others(23): Show |
intron_variant | MODIFIER | HG01884.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0120 | 1 | 272 | 0.0037 | 30 | c.411 others(47): Show |
FAM107B | ENSG00000065809.14 | transcript | ENST00000181796.7 | protein_coding | 1/4 | chr10 | TogoVar | |||||||
FAM107B_chr10_14513557_14779897 | 14767055 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | HG01255.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0104 | 1 | 272 | 0.0037 | 30 | c.411 others(47): Show |
FAM107B | ENSG00000065809.14 | transcript | ENST00000181796.7 | protein_coding | 1/4 | chr10 | TogoVar | |||||||
FAM107B_chr10_14513557_14779897 | 14767055 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | HG03831.hp2 | a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0226 | 1 | 272 | 0.0037 | 30 | c.411 others(47): Show |
FAM107B | ENSG00000065809.14 | transcript | ENST00000181796.7 | protein_coding | 1/4 | chr10 | TogoVar | |||||||
FAM107B_chr10_14513557_14779897 | 14767055 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | HG01934.hp2 NA19063.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0007 a0001c0001t0002g0067 |
2 | 272 | 0.0074 | 30 | c.411 others(47): Show |
FAM107B | ENSG00000065809.14 | transcript | ENST00000181796.7 | protein_coding | 1/4 | chr10 | TogoVar | |||||||
FAM110B_chr8_57989523_58153784 | 58006901 | G | GTATATAT others(23): Show |
intron_variant | MODIFIER | HG01255.hp1 HG02027.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0230 a0001c0001t0006g0155 |
2 | 300 | 0.0067 | 30 | c.-51 others(51): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
FAM110B_chr8_57989523_58153784 | 58006923 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG02965.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0294 | 1 | 300 | 0.0033 | 30 | c.-51 others(51): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
FAM110B_chr8_57989523_58153784 | 58047591 | C | CCTCTCTC others(23): Show |
intron_variant | MODIFIER | HG00408.hp2 HG02717.hp1 NA19084.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0007 | a0001c0001t0002g0240 a0001c0001t0003g0255 a0001c0001t0007g0300 |
3 | 300 | 0.0100 | 30 | c.-41 others(51): Show |
FAM110B | ENSG00000169122.12 | transcript | ENST00000519262.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
FAM114A1_chr4_38862806_38950739 | 38880095 | A | AAATAGAG others(23): Show |
intron_variant | MODIFIER | HG02280.hp1 | a0002 | a0002c0003 | a0002c0003t0005 | a0002c0003t0005g0339 | 1 | 372 | 0.0027 | 30 | c.348 others(47): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
FAM114A1_chr4_38862806_38950739 | 38880107 | G | GTAGAATA others(23): Show |
intron_variant | MODIFIER | HG02809.hp2 HG03834.hp1 |
a0007a0012 | a0007c0021a0012c0051 | a0007c0021t0013a0012c0051t0005 | a0007c0021t0013g0340 a0012c0051t0005g0344 |
2 | 372 | 0.0054 | 30 | c.348 others(47): Show |
FAM114A1 | ENSG00000197712.12 | transcript | ENST00000358869.5 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
FAM120A_chr9_93446685_93571112 | 93545780 | C | CTTTTTTT others(23): Show |
intron_variant | MODIFIER | HG02717.hp1 NA19087.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003 | a0001c0001t0002g0098 a0001c0001t0003g0082 |
2 | 318 | 0.0063 | 30 | c.215 others(49): Show |
FAM120A | ENSG00000048828.18 | transcript | ENST00000277165.11 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr9 | TogoVar | ||||||
FAM120B_chr6_170301758_170412067 | 170381140 | T | TTATGCTC others(23): Show |
intron_variant | MODIFIER | NA19001.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0053 | 1 | 289 | 0.0035 | 30 | c.228 others(49): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||||
FAM120B_chr6_170301758_170412067 | 170407726 | C | CAGACAAA others(23): Show |
downstream_gene_variant | MODIFIER | HG03710.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0201 | 1 | 289 | 0.0035 | 30 | c.*29 others(41): Show |
FAM120B | ENSG00000112584.14 | transcript | ENST00000476287.4 | protein_coding | 660 | chr6 | TogoVar | |||||||
FAM120C_chrX_54063324_54188254 | 54117354 | A | AAAAATAA others(23): Show |
intron_variant | MODIFIER | HG00621.hp1 HG01167.hp1 HG01169.hp1 |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0017 | a0001c0001t0008g0158 a0001c0001t0017g0005 a0001c0001t0017g0171 |
3 | 190 | 0.0158 | 30 | c.206 others(47): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | TogoVar | |||||||
FAM131C_chr1_16052769_16078651 | 16058340 | G | GATGCCCT others(23): Show |
3_prime_UTR_variant | MODIFIER | HG02258.hp2 | a0002 | a0002c0002 | a0002c0002t0019 | a0002c0002t0019g0135 | 1 | 376 | 0.0027 | 30 | c.*67 others(37): Show |
FAM131C | ENSG00000185519.9 | transcript | ENST00000375662.5 | protein_coding | 7/7 | 96 | chr1 | TogoVar | ||||||
FAM135B_chr8_138125023_138502261 | 138226184 | T | TGTGTGTG others(23): Show |
intron_variant | MODIFIER | homoSapiens_chm13v2.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0070 | 1 | 212 | 0.0047 | 30 | c.669 others(49): Show |
FAM135B | ENSG00000147724.12 | transcript | ENST00000395297.6 | protein_coding | 7/19 | chr8 | TogoVar | |||||||
FAM13A_chr4_88720960_89062185 | 88945990 | G | GTATGTAT others(23): Show |
intron_variant | MODIFIER | HG02258.hp1 | a0001 | a0001c0009 | a0001c0009t0033 | a0001c0009t0033g0200 | 1 | 208 | 0.0048 | 30 | c.606 others(47): Show |
FAM13A | ENSG00000138640.15 | transcript | ENST00000264344.10 | protein_coding | 4/23 | chr4 | TogoVar | |||||||
FAM13A_chr4_88720960_89062185 | 88945990 | G | GTGTGTGT others(23): Show |
intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0003 | a0001c0003t0024 | a0001c0003t0024g0057 | 1 | 208 | 0.0048 | 30 | c.606 others(47): Show |
FAM13A | ENSG00000138640.15 | transcript | ENST00000264344.10 | protein_coding | 4/23 | chr4 | TogoVar | |||||||
FAM13C_chr10_59241133_59367549 | 59286516 | A | AATATATA others(23): Show |
intron_variant | MODIFIER | NA18959.hp1 NA20300.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0089 a0001c0001t0002g0014 |
2 | 204 | 0.0098 | 30 | c.508 others(47): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | TogoVar | |||||||
FAM13C_chr10_59241133_59367549 | 59304761 | G | GAGGGAAG others(23): Show |
intron_variant | MODIFIER | HG00609.hp2 HG00738.hp2 HG01081.hp2 others(17): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0002a0001c0006t0001 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0042 others(17): Show |
20 | 204 | 0.0980 | 30 | c.444 others(47): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | TogoVar | |||||||
FAM13C_chr10_59241133_59367549 | 59304761 | G | GAGGGAAG others(23): Show |
intron_variant | MODIFIER | HG00558.hp2 HG01106.hp1 HG01167.hp1 others(16): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0001 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0001g0054 others(15): Show |
19 | 204 | 0.0931 | 30 | c.444 others(47): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | TogoVar | |||||||
FAM13C_chr10_59241133_59367549 | 59304786 | A | AAAGGAAG others(23): Show |
intron_variant | MODIFIER | NA19090.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0073 | 1 | 204 | 0.0049 | 30 | c.444 others(47): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | TogoVar | |||||||
FAM149A_chr4_186099704_186180337 | 186130293 | C | CTCTCTCT others(23): Show |
intron_variant | MODIFIER | NA18943.hp2 | a0003 | a0003c0002 | a0003c0002t0004 | a0003c0002t0004g0325 | 1 | 390 | 0.0026 | 30 | c.567 others(49): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
FAM149A_chr4_186099704_186180337 | 186130293 | C | CTCTCTCT others(23): Show |
intron_variant | MODIFIER | HG02132.hp2 NA18953.hp1 NA18964.hp2 |
a0001a0002a0003 | a0001c0001a0002c0004a0003c0002 | a0001c0001t0001a0002c0004t0001a0003c0002t0004 | a0001c0001t0001g0119 a0002c0004t0001g0120 a0003c0002t0004g0344 |
3 | 390 | 0.0077 | 30 | c.567 others(49): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
FAM149A_chr4_186099704_186180337 | 186130293 | C | CTCTCTCT others(23): Show |
intron_variant | MODIFIER | HG00558.hp1 NA18985.hp2 |
a0003 | a0003c0002 | a0003c0002t0004 | a0003c0002t0004g0352 a0003c0002t0004g0372 |
2 | 390 | 0.0051 | 30 | c.567 others(49): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
FAM149A_chr4_186099704_186180337 | 186130293 | C | CTCTCTCT others(23): Show |
intron_variant | MODIFIER | NA18990.hp2 NA18992.hp1 |
a0003a0009 | a0003c0002a0009c0015 | a0003c0002t0004a0009c0015t0003 | a0003c0002t0004g0346 a0009c0015t0003g0299 |
2 | 390 | 0.0051 | 30 | c.567 others(49): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
FAM149A_chr4_186099704_186180337 | 186130293 | C | CTCTCTCT others(23): Show |
intron_variant | MODIFIER | HG02080.hp1 | a0003 | a0003c0002 | a0003c0002t0004 | a0003c0002t0004g0373 | 1 | 390 | 0.0026 | 30 | c.567 others(49): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
FAM149A_chr4_186099704_186180337 | 186136936 | A | ATCTCTCT others(23): Show |
intron_variant | MODIFIER | HG03927.hp2 | a0003 | a0003c0002 | a0003c0002t0004 | a0003c0002t0004g0338 | 1 | 390 | 0.0026 | 30 | c.567 others(49): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
FAM149B1_chr10_73163119_73249504 | 73169951 | T | TTATTAAT others(23): Show |
intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(100): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0002c0009others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0044 a0001c0001t0002g0059 a0001c0001t0003g0217 others(100): Show |
103 | 236 | 0.4364 | 30 | c.47+ others(45): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
FAM151B_chr5_80483100_80547563 | 80538448 | C | CTTTCTCT others(23): Show |
intron_variant | MODIFIER | HG01168.hp1 HG01169.hp2 |
a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0001 | 2 | 356 | 0.0056 | 30 | c.672 others(47): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
FAM151B_chr5_80483100_80547563 | 80538450 | C | CTTTCTTT others(23): Show |
intron_variant | MODIFIER | HG01109.hp2 HG01884.hp1 HG03041.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0003t0001 | a0001c0001t0002g0285 a0001c0003t0001g0292 a0001c0003t0001g0294 |
3 | 356 | 0.0084 | 30 | c.672 others(47): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
FAM161A_chr2_61819848_61859060 | 61823362 | C | CATATATA others(23): Show |
downstream_gene_variant | MODIFIER | HG03225.hp1 NA18962.hp1 NA18997.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0002 | a0001c0001t0002g0218 a0002c0002t0002g0232 a0002c0002t0002g0273 |
3 | 400 | 0.0075 | 30 | c.*30 others(41): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1485 | chr2 | TogoVar | |||||||
FAM162B_chr6_116747197_116770719 | 116752711 | A | AATATATA others(23): Show |
intron_variant | MODIFIER | HG02965.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0161 | 1 | 474 | 0.0021 | 30 | c.391 others(43): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | TogoVar | |||||||
FAM163A_chr1_179738291_179821198 | 179795958 | C | CTATTATT others(23): Show |
intron_variant | MODIFIER | HG00609.hp1 HG01069.hp2 HG01109.hp2 others(20): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(9): Show | a0001c0001t0002g0052 a0001c0001t0002g0071 a0001c0001t0005g0034 others(19): Show |
23 | 226 | 0.1018 | 30 | c.-13 others(51): Show |
FAM163A | ENSG00000143340.7 | transcript | ENST00000341785.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
FAM171A2_chr17_44348215_44368853 | 44357730 | C | CGTGTGTG others(23): Show |
intron_variant | MODIFIER | NA19065.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0074 | 1 | 416 | 0.0024 | 30 | c.440 others(47): Show |
FAM171A2 | ENSG00000161682.15 | transcript | ENST00000293443.12 | protein_coding | 3/7 | chr17 | TogoVar | |||||||
FAM172A_chr5_93612725_94116663 | 94035196 | C | CATACATA others(23): Show |
intron_variant | MODIFIER | HG03225.hp1 HG03579.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0002c0002t0006 | a0001c0001t0002g0029 a0002c0002t0006g0084 |
2 | 126 | 0.0159 | 30 | c.309 others(49): Show |
FAM172A | ENSG00000113391.19 | transcript | ENST00000395965.8 | protein_coding | 4/10 | chr5 | TogoVar |