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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
FAM13B_chr5_137932960_138038079 | 137975980 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG03209.hp2 NA19030.hp2 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0166 a0001c0001t0002g0250 |
2 | 322 | 0.0062 | 18 | c.117 others(37): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | TogoVar | |||||||
FAM13B_chr5_137932960_138038079 | 138034995 | C | CTTTTTTT others(11): Show |
upstream_gene_variant | MODIFIER | HG03710.hp2 NA18994.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0093 a0001c0001t0001g0103 |
2 | 322 | 0.0062 | 18 | c.-24 others(29): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1917 | chr5 | TogoVar | |||||||
FAM13C_chr10_59241133_59367549 | 59269417 | T | TACACACA others(11): Show |
intron_variant | MODIFIER | HG02135.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0104 | 1 | 204 | 0.0049 | 18 | c.803 others(33): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 7/13 | chr10 | TogoVar | |||||||
FAM13C_chr10_59241133_59367549 | 59286516 | A | AATATATA others(11): Show |
intron_variant | MODIFIER | HG02258.hp2 HG02280.hp1 HG02723.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0070 a0001c0001t0001g0107 a0001c0001t0001g0153 others(1): Show |
4 | 204 | 0.0196 | 18 | c.508 others(35): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 5/13 | chr10 | TogoVar | |||||||
FAM149A_chr4_186099704_186180337 | 186110341 | C | CCTCAGGG others(11): Show |
intron_variant | MODIFIER | HG00323.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0377 | 1 | 390 | 0.0026 | 18 | c.566 others(35): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
FAM149A_chr4_186099704_186180337 | 186130263 | A | ATCTCTCT others(11): Show |
intron_variant | MODIFIER | HG00438.hp2 HG03239.hp1 |
a0001a0003 | a0001c0010a0003c0002 | a0001c0010t0005a0003c0002t0091 | a0001c0010t0005g0254 a0003c0002t0091g0323 |
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 | 186130293 | C | CTATATAT others(11): Show |
intron_variant | MODIFIER | HG01243.hp1 | a0004 | a0004c0003 | a0004c0003t0003 | a0004c0003t0003g0152 | 1 | 390 | 0.0026 | 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 | 186130293 | C | CTCTATAT others(11): Show |
intron_variant | MODIFIER | HG02896.hp2 HG02897.hp1 |
a0001 | a0001c0001 | a0001c0001t0029 | a0001c0001t0029g0228 a0001c0001t0029g0229 |
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 | 186130293 | C | CTCTCTAT others(11): Show |
intron_variant | MODIFIER | HG00323.hp2 HG01169.hp2 HG02083.hp2 others(2): Show |
a0001a0003 | a0001c0001a0003c0012 | a0001c0001t0001a0001c0001t0018a0003c0012t0030others(1): Show | a0001c0001t0001g0072 a0001c0001t0001g0132 a0001c0001t0018g0104 others(2): Show |
5 | 390 | 0.0128 | 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 | 186130293 | C | CTCTCTCT others(11): Show |
intron_variant | MODIFIER | NA18959.hp1 NA19062.hp1 NA19064.hp2 |
a0001a0006 | a0001c0001a0001c0020a0006c0023 | a0001c0001t0002a0001c0020t0005a0006c0023t0080 | a0001c0001t0002g0049 a0001c0020t0005g0259 a0006c0023t0080g0127 |
3 | 390 | 0.0077 | 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 | 186130293 | C | CTCTCTCT others(11): Show |
intron_variant | MODIFIER | HG02080.hp2 HG03704.hp2 NA18971.hp2 others(2): Show |
a0001a0032 | a0001c0001a0001c0005a0001c0010others(1): Show | a0001c0001t0002a0001c0005t0002a0001c0010t0056others(1): Show | a0001c0001t0002g0050 a0001c0001t0002g0151 a0001c0005t0002g0085 others(2): Show |
5 | 390 | 0.0128 | 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 | 186130293 | C | CTCTCTCT others(11): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00673.hp2 HG02155.hp1 others(5): Show |
a0001a0002a0003 | a0001c0001a0001c0005a0002c0007others(1): Show | a0001c0001t0001a0001c0001t0082a0001c0005t0002others(2): Show | a0001c0001t0001g0034 a0001c0001t0001g0088 a0001c0001t0082g0044 others(5): Show |
8 | 390 | 0.0205 | 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 | 186130293 | C | CTCTCTCT others(11): Show |
intron_variant | MODIFIER | HG00738.hp2 HG02074.hp2 |
a0001 | a0001c0001a0001c0031 | a0001c0001t0019a0001c0031t0002 | a0001c0001t0019g0033 a0001c0031t0002g0107 |
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 | 186130293 | C | CTCTCTCT others(11): Show |
intron_variant | MODIFIER | HG03710.hp1 NA18612.hp2 NA18940.hp1 others(1): Show |
a0001a0005a0030 | a0001c0005a0005c0006a0030c0041 | a0001c0005t0002a0005c0006t0007a0030c0041t0001 | a0001c0005t0002g0042 a0001c0005t0002g0043 a0005c0006t0007g0095 others(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 | 186130293 | C | CTCTCTCT others(11): Show |
intron_variant | MODIFIER | HG03491.hp2 HG03927.hp2 NA18612.hp1 others(1): Show |
a0001a0002a0003 | a0001c0001a0002c0007a0003c0002 | a0001c0001t0010a0002c0007t0011a0003c0002t0004 | a0001c0001t0010g0337 a0002c0007t0011g0252 a0002c0007t0011g0274 others(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 | 186130314 | T | TATATATA others(11): Show |
intron_variant | MODIFIER | NA18995.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0047 | 1 | 390 | 0.0026 | 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 | 186136940 | C | CTCTCTCT others(11): Show |
intron_variant | MODIFIER | HG01256.hp1 HG01258.hp2 |
a0006 | a0006c0009 | a0006c0009t0008 | a0006c0009t0008g0002 | 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 | 186176950 | T | TGTGTGTG others(11): Show |
downstream_gene_variant | MODIFIER | HG02280.hp2 NA19240.hp1 |
a0006 | a0006c0018 | a0006c0018t0026 | a0006c0018t0026g0266 a0006c0018t0026g0269 |
2 | 390 | 0.0051 | 18 | c.*49 others(29): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 1614 | chr4 | TogoVar | |||||||
FAM151B_chr5_80483100_80547563 | 80490019 | T | TACACACA others(11): Show |
intron_variant | MODIFIER | HG03471.hp1 HG04115.hp2 NA18612.hp2 |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0016 a0002c0002t0001g0017 a0002c0002t0001g0018 |
3 | 356 | 0.0084 | 18 | c.25+ others(33): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
FAM151B_chr5_80483100_80547563 | 80538426 | T | TTCTTTCT others(11): Show |
intron_variant | MODIFIER | NA20905.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0291 | 1 | 356 | 0.0028 | 18 | c.672 others(35): 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(11): Show |
downstream_gene_variant | MODIFIER | HG00738.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0219 | 1 | 400 | 0.0025 | 18 | c.*30 others(29): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1485 | chr2 | TogoVar | |||||||
FAM162B_chr6_116747197_116770719 | 116752711 | A | AATATATA others(11): Show |
intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0167 | 1 | 474 | 0.0021 | 18 | c.391 others(31): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | TogoVar | |||||||
FAM162B_chr6_116747197_116770719 | 116761650 | A | ATATATAT others(11): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(7): Show | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(172): Show |
278 | 474 | 0.5865 | 18 | c.390 others(33): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | TogoVar | |||||||
FAM162B_chr6_116747197_116770719 | 116761660 | T | TTATATAT others(11): Show |
intron_variant | MODIFIER | HG02257.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0232 | 1 | 474 | 0.0021 | 18 | c.390 others(33): Show |
FAM162B | ENSG00000183807.8 | transcript | ENST00000368557.6 | protein_coding | 3/3 | chr6 | TogoVar | |||||||
FAM163A_chr1_179738291_179821198 | 179795958 | C | CTATTATT others(11): Show |
intron_variant | MODIFIER | HG01952.hp2 HG02129.hp2 HG02145.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0037a0001c0001t0059 | a0001c0001t0002g0036 a0001c0001t0002g0041 a0001c0001t0002g0046 others(6): Show |
9 | 226 | 0.0398 | 18 | c.-13 others(39): Show |
FAM163A | ENSG00000143340.7 | transcript | ENST00000341785.5 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
FAM163B_chr9_133572081_133614389 | 133590213 | C | CCTCTCTC others(11): Show |
intron_variant | MODIFIER | HG02615.hp1 HG02818.hp1 HG03041.hp1 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0026 a0001c0001t0005g0090 |
3 | 382 | 0.0079 | 18 | c.-23 others(35): Show |
FAM163B | ENSG00000196990.10 | transcript | ENST00000673969.1 | protein_coding | 1/2 | chr9 | TogoVar | |||||||
FAM167A_chr8_11416476_11471753 | 11422373 | G | GGGGTGTG others(11): Show |
3_prime_UTR_variant | MODIFIER | HG04204.hp2 | a0001 | a0001c0001 | a0001c0001t0091 | a0001c0001t0091g0140 | 1 | 374 | 0.0027 | 18 | c.*19 others(29): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 3/3 | 1999 | chr8 | TogoVar | ||||||
FAM167A_chr8_11416476_11471753 | 11455891 | C | CTGAGTGT others(11): Show |
intron_variant | MODIFIER | HG02630.hp2 HG02886.hp1 HG03516.hp2 others(1): Show |
a0001 | a0001c0001a0001c0009 | a0001c0001t0009a0001c0009t0009 | a0001c0001t0009g0255 a0001c0001t0009g0256 a0001c0001t0009g0257 others(1): Show |
4 | 374 | 0.0107 | 18 | c.-39 others(39): Show |
FAM167A | ENSG00000154319.16 | transcript | ENST00000284486.9 | protein_coding | 1/2 | chr8 | TogoVar | |||||||
FAM168A_chr11_73395487_73603112 | 73426703 | C | CTGTGTGT others(11): Show |
intron_variant | MODIFIER | HG01167.hp2 HG01934.hp2 HG02683.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0007a0001c0001t0024 | a0001c0001t0007g0022 a0001c0001t0007g0023 a0001c0001t0007g0026 others(2): Show |
5 | 180 | 0.0278 | 18 | c.151 others(35): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 3/7 | chr11 | TogoVar | |||||||
FAM168A_chr11_73395487_73603112 | 73442955 | G | GATATATA others(11): Show |
intron_variant | MODIFIER | NA18983.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0163 | 1 | 180 | 0.0056 | 18 | c.71- others(35): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | TogoVar | |||||||
FAM168A_chr11_73395487_73603112 | 73445419 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG02615.hp1 NA19080.hp2 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0016 | a0001c0001t0003g0170 a0001c0001t0016g0136 |
2 | 180 | 0.0111 | 18 | c.71- others(35): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | TogoVar | |||||||
FAM168A_chr11_73395487_73603112 | 73496873 | T | TCACACAC others(11): Show |
intron_variant | MODIFIER | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0011 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0011g0149 others(1): Show |
4 | 180 | 0.0222 | 18 | c.-18 others(37): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | TogoVar | |||||||
FAM168B_chr2_131042876_131098460 | 131087063 | C | CAAAAAAA others(11): Show |
intron_variant | MODIFIER | HG01884.hp2 HG03516.hp2 NA19240.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008 | a0001c0001t0001g0144 a0001c0001t0008g0054 a0001c0001t0008g0055 |
3 | 260 | 0.0115 | 18 | c.-11 others(35): Show |
FAM168B | ENSG00000152102.18 | transcript | ENST00000389915.4 | protein_coding | 1/6 | chr2 | TogoVar | |||||||
FAM169A_chr5_74772574_74871387 | 74784510 | C | CAAAAAAA others(11): Show |
intron_variant | MODIFIER | NA20129.hp2 | a0001 | a0001c0003 | a0001c0003t0006 | a0001c0003t0006g0225 | 1 | 308 | 0.0033 | 18 | c.126 others(37): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 11/12 | chr5 | TogoVar | |||||||
FAM169A_chr5_74772574_74871387 | 74805524 | C | CTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG01884.hp2 HG02647.hp2 HG03209.hp2 |
a0001 | a0001c0002 | a0001c0002t0006 | a0001c0002t0006g0017 a0001c0002t0006g0018 a0001c0002t0006g0020 |
3 | 308 | 0.0097 | 18 | c.671 others(33): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 6/12 | chr5 | TogoVar | |||||||
FAM171A1_chr10_15206643_15376289 | 15331859 | G | GTATACAT others(11): Show |
intron_variant | MODIFIER | NA19087.hp1 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0294 | 1 | 303 | 0.0033 | 18 | c.97+ others(35): Show |
FAM171A1 | ENSG00000148468.17 | transcript | ENST00000378116.9 | protein_coding | 1/7 | chr10 | TogoVar | |||||||
FAM171A1_chr10_15206643_15376289 | 15331859 | G | GTGTATAC others(11): Show |
intron_variant | MODIFIER | NA18957.hp1 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0186 | 1 | 303 | 0.0033 | 18 | c.97+ others(35): Show |
FAM171A1 | ENSG00000148468.17 | transcript | ENST00000378116.9 | protein_coding | 1/7 | chr10 | TogoVar | |||||||
FAM171A2_chr17_44348215_44368853 | 44357730 | C | CGTGTGTG others(11): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(11): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0003 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(2): Show | a0001c0001t0001g0014 a0001c0001t0001g0020 a0001c0001t0001g0084 others(5): Show |
14 | 416 | 0.0337 | 18 | c.440 others(35): Show |
FAM171A2 | ENSG00000161682.15 | transcript | ENST00000293443.12 | protein_coding | 3/7 | chr17 | TogoVar | |||||||
FAM171A2_chr17_44348215_44368853 | 44368119 | A | AATATATA others(11): Show |
upstream_gene_variant | MODIFIER | HG02129.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 416 | 0.0024 | 18 | c.-44 others(29): Show |
FAM171A2 | ENSG00000161682.15 | transcript | ENST00000293443.12 | protein_coding | 4267 | chr17 | TogoVar | |||||||
FAM171A2_chr17_44348215_44368853 | 44368146 | A | ATATATAT others(11): Show |
upstream_gene_variant | MODIFIER | HG03486.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0028 | 1 | 416 | 0.0024 | 18 | c.-44 others(29): Show |
FAM171A2 | ENSG00000161682.15 | transcript | ENST00000293443.12 | protein_coding | 4294 | chr17 | TogoVar | |||||||
FAM171B_chr2_186689060_186770959 | 186689965 | C | CGTGTGTG others(11): Show |
upstream_gene_variant | MODIFIER | HG00558.hp1 HG03239.hp2 HG04199.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0016 | a0001c0001t0010a0001c0002t0005a0001c0002t0016others(1): Show | a0001c0001t0010g0279 a0001c0002t0005g0241 a0001c0002t0016g0226 others(1): Show |
4 | 332 | 0.0121 | 18 | c.-42 others(29): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 4094 | chr2 | TogoVar | |||||||
FAM171B_chr2_186689060_186770959 | 186736538 | C | CTGTGTGT others(11): Show |
intron_variant | MODIFIER | HG03710.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0267 | 1 | 332 | 0.0030 | 18 | c.239 others(35): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
FAM172A_chr5_93612725_94116663 | 93635459 | G | GTTTTTTT others(11): Show |
intron_variant | MODIFIER | HG02486.hp2 NA20129.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004 | a0001c0001t0002g0118 a0001c0001t0004g0089 |
2 | 126 | 0.0159 | 18 | c.110 others(39): Show |
FAM172A | ENSG00000113391.19 | transcript | ENST00000395965.8 | protein_coding | 10/10 | chr5 | TogoVar | |||||||
FAM172A_chr5_93612725_94116663 | 93779124 | T | TGTGTGTG others(11): Show |
intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0029 | 1 | 126 | 0.0079 | 18 | c.102 others(37): Show |
FAM172A | ENSG00000113391.19 | transcript | ENST00000395965.8 | protein_coding | 9/10 | chr5 | TogoVar | |||||||
FAM172A_chr5_93612725_94116663 | 93830297 | A | ATATATGT others(11): Show |
intron_variant | MODIFIER | HG03516.hp2 NA19003.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004 | a0001c0001t0002g0122 a0001c0001t0004g0013 |
2 | 126 | 0.0159 | 18 | c.787 others(35): Show |
FAM172A | ENSG00000113391.19 | transcript | ENST00000395965.8 | protein_coding | 7/10 | chr5 | TogoVar | |||||||
FAM172A_chr5_93612725_94116663 | 93830299 | A | ATATGTGT others(11): Show |
intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0025 | 1 | 126 | 0.0079 | 18 | c.787 others(35): Show |
FAM172A | ENSG00000113391.19 | transcript | ENST00000395965.8 | protein_coding | 7/10 | chr5 | TogoVar | |||||||
FAM172A_chr5_93612725_94116663 | 93830311 | G | GTGTATGT others(11): Show |
intron_variant | MODIFIER | HG00597.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0104 | 1 | 126 | 0.0079 | 18 | c.787 others(35): Show |
FAM172A | ENSG00000113391.19 | transcript | ENST00000395965.8 | protein_coding | 7/10 | chr5 | TogoVar | |||||||
FAM172A_chr5_93612725_94116663 | 93830311 | G | GTGTATGT others(11): Show |
intron_variant | MODIFIER | HG01168.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0085 | 1 | 126 | 0.0079 | 18 | c.787 others(35): Show |
FAM172A | ENSG00000113391.19 | transcript | ENST00000395965.8 | protein_coding | 7/10 | chr5 | TogoVar | |||||||
FAM172A_chr5_93612725_94116663 | 93830311 | G | GTGTGTAT others(11): Show |
intron_variant | MODIFIER | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0005 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0001g0069 others(13): Show |
16 | 126 | 0.1270 | 18 | c.787 others(35): Show |
FAM172A | ENSG00000113391.19 | transcript | ENST00000395965.8 | protein_coding | 7/10 | chr5 | TogoVar | |||||||
FAM172A_chr5_93612725_94116663 | 94035196 | C | CATACATA others(11): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00544.hp2 HG01099.hp2 others(19): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0036 a0001c0001t0001g0045 a0001c0001t0001g0068 others(19): Show |
22 | 126 | 0.1746 | 18 | c.309 others(37): Show |
FAM172A | ENSG00000113391.19 | transcript | ENST00000395965.8 | protein_coding | 4/10 | chr5 | TogoVar |