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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
FAM13A_chr4_88720960_89062185 | 89061579 | GTTTTTTT others(7): Show |
G | upstream_gene_variant | MODIFIER | HG00639.hp2 HG02895.hp2 NA18906.hp1 |
a0001a0002 | a0001c0003a0001c0005a0002c0004 | a0001c0003t0026a0001c0005t0012a0002c0004t0010 | a0001c0003t0026g0052a0001c0005t0012g0053a0002c0004t0010g0056 | 3 | 208 | 0.0144 | -14 | c.-46 others(25): Show |
FAM13A | ENSG00000138640.15 | transcript | ENST00000264344.10 | protein_coding | 4395 | chr4 | TogoVar | ||||||
FAM13B_chr5_137932960_138038079 | 137981077 | ATTTTTTT others(7): Show |
A | intron_variant | MODIFIER | HG00642.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0284 | 1 | 322 | 0.0031 | -14 | c.117 others(33): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | TogoVar | ||||||
FAM13B_chr5_137932960_138038079 | 137983176 | TAAAAAAA others(7): Show |
T | intron_variant | MODIFIER | HG01081.hp1 HG01361.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0047a0001c0001t0002g0056 | 2 | 322 | 0.0062 | -14 | c.117 others(33): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | TogoVar | ||||||
FAM13B_chr5_137932960_138038079 | 137984199 | GATTATTT others(7): Show |
G | intron_variant | MODIFIER | HG00741.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0073 | 1 | 322 | 0.0031 | -14 | c.117 others(33): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 10/23 | chr5 | TogoVar | ||||||
FAM13B_chr5_137932960_138038079 | 138034995 | CTTTTTTT others(7): Show |
C | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00642.hp1 HG01346.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0001g0172others(4): Show | 7 | 322 | 0.0217 | -14 | c.-24 others(25): Show |
FAM13B | ENSG00000031003.11 | transcript | ENST00000689681.1 | protein_coding | 1917 | chr5 | TogoVar | ||||||
FAM13C_chr10_59241133_59367549 | 59319107 | ACACACAC others(7): Show |
A | intron_variant | MODIFIER | HG02572.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 4 | 204 | 0.0196 | -14 | c.443 others(31): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 4/13 | chr10 | TogoVar | ||||||
FAM13C_chr10_59241133_59367549 | 59360853 | GAAAAAAA others(7): Show |
G | intron_variant | MODIFIER | HG01070.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0169a0001c0001t0001g0172a0001c0001t0001g0173others(8): Show | 11 | 204 | 0.0539 | -14 | c.62+ others(29): Show |
FAM13C | ENSG00000148541.13 | transcript | ENST00000618804.5 | protein_coding | 1/13 | chr10 | TogoVar | ||||||
FAM149A_chr4_186099704_186180337 | 186104741 | CGCGGGCG others(7): Show |
C | 5_prime_UTR_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(66): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0005a0002c0004others(7): Show | a0001c0001t0004a0001c0001t0010a0001c0001t0012others(15): Show | a0001c0001t0004g0332a0001c0001t0004g0347a0001c0001t0010g0333others(66): Show | 69 | 390 | 0.1769 | -14 | c.-32 others(23): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 1/14 | 308 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||
FAM149A_chr4_186099704_186180337 | 186136950 | CTCTCTCT others(7): Show |
C | intron_variant | MODIFIER | HG01256.hp2 | a0021 | a0021c0046 | a0021c0046t0016 | a0021c0046t0016g0003 | 1 | 390 | 0.0026 | -14 | c.567 others(33): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
FAM149A_chr4_186099704_186180337 | 186136962 | CTTTCTCT others(7): Show |
C | intron_variant | MODIFIER | HG00597.hp1 HG01109.hp2 HG01993.hp2 others(10): Show |
a0001a0003a0004others(5): Show | a0001c0001a0003c0002a0004c0003others(7): Show | a0001c0001t0078a0003c0002t0004a0004c0003t0003others(8): Show | a0001c0001t0078g0032a0003c0002t0004g0370a0004c0003t0003g0176others(10): Show | 13 | 390 | 0.0333 | -14 | c.567 others(33): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
FAM149A_chr4_186099704_186180337 | 186136964 | TTCTCTCT others(7): Show |
T | intron_variant | MODIFIER | HG00140.hp2 HG01496.hp1 HG02738.hp1 |
a0001a0003 | a0001c0001a0003c0012 | a0001c0001t0001a0003c0012t0005 | a0001c0001t0001g0034a0001c0001t0001g0035a0003c0012t0005g0250 | 3 | 390 | 0.0077 | -14 | c.567 others(33): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
FAM149A_chr4_186099704_186180337 | 186140441 | CTTTTTTT others(7): Show |
C | intron_variant | MODIFIER | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
a0001a0002a0005others(2): Show | a0001c0040a0002c0004a0002c0007others(3): Show | a0001c0040t0009a0002c0004t0003a0002c0004t0045others(5): Show | a0001c0040t0009g0294a0002c0004t0003g0387a0002c0004t0045g0309others(5): Show | 8 | 390 | 0.0205 | -14 | c.567 others(31): Show |
FAM149A | ENSG00000109794.14 | transcript | ENST00000706927.1 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
FAM149B1_chr10_73163119_73249504 | 73204944 | ATTTTTTT others(7): Show |
A | intron_variant | MODIFIER | HG02559.hp1 HG02976.hp2 HG03209.hp1 others(2): Show |
a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0112a0003c0003t0001g0121a0003c0003t0001g0125others(2): Show | 5 | 236 | 0.0212 | -14 | c.543 others(31): Show |
FAM149B1 | ENSG00000138286.15 | transcript | ENST00000242505.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | |||||
FAM151B_chr5_80483100_80547563 | 80538450 | CTTTCTTT others(7): Show |
C | intron_variant | MODIFIER | HG00323.hp1 HG02080.hp2 HG03654.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0049a0001c0001t0001g0208a0001c0001t0001g0305others(1): Show | 4 | 356 | 0.0112 | -14 | c.672 others(31): Show |
FAM151B | ENSG00000152380.10 | transcript | ENST00000282226.5 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
FAM161A_chr2_61819848_61859060 | 61849056 | TTATATAT others(7): Show |
T | intron_variant | MODIFIER | HG03209.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0141 | 1 | 400 | 0.0025 | -14 | c.183 others(31): Show |
FAM161A | ENSG00000170264.13 | transcript | ENST00000404929.6 | protein_coding | 1/6 | chr2 | TogoVar | ||||||
FAM161B_chr14_73927276_73955094 | 73937018 | CACTGCCT others(7): Show |
C | intron_variant | MODIFIER | NA18972.hp2 | a0003 | a0003c0004 | a0003c0004t0004 | a0003c0004t0004g0142 | 1 | 442 | 0.0023 | -14 | c.166 others(31): Show |
FAM161B | ENSG00000156050.10 | transcript | ENST00000286544.5 | protein_coding | 7/8 | chr14 | TogoVar | ||||||
FAM163A_chr1_179738291_179821198 | 179815103 | GCGCGCGC others(7): Show |
G | 3_prime_UTR_variant | MODIFIER | HG02109.hp1 | a0001 | a0001c0001 | a0001c0001t0036 | a0001c0001t0036g0161 | 1 | 226 | 0.0044 | -14 | c.*91 others(23): Show |
FAM163A | ENSG00000143340.7 | transcript | ENST00000341785.5 | protein_coding | 5/5 | 916 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||
FAM163A_chr1_179738291_179821198 | 179815105 | GCGCGCAC others(7): Show |
G | 3_prime_UTR_variant | MODIFIER | HG01884.hp1 HG02486.hp2 HG02622.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0015a0001c0001t0025a0001c0001t0026 | a0001c0001t0015g0006a0001c0001t0015g0105a0001c0001t0015g0118others(4): Show | 8 | 226 | 0.0354 | -14 | c.*91 others(23): Show |
FAM163A | ENSG00000143340.7 | transcript | ENST00000341785.5 | protein_coding | 5/5 | 918 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||
FAM163B_chr9_133572081_133614389 | 133600259 | CTGTGTGT others(7): Show |
C | intron_variant | MODIFIER | HG01361.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0109 | 1 | 382 | 0.0026 | -14 | c.-24 others(31): Show |
FAM163B | ENSG00000196990.10 | transcript | ENST00000673969.1 | protein_coding | 1/2 | chr9 | TogoVar | ||||||
FAM168A_chr11_73395487_73603112 | 73442955 | GATATATA others(7): Show |
G | intron_variant | MODIFIER | HG02109.hp1 NA21309.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0010a0001c0002t0032 | a0001c0001t0010g0004a0001c0002t0032g0116 | 2 | 180 | 0.0111 | -14 | c.71- others(31): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | TogoVar | ||||||
FAM168A_chr11_73395487_73603112 | 73445419 | CTTTTTTT others(7): Show |
C | intron_variant | MODIFIER | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0017a0001c0001t0018 | a0001c0001t0017g0032a0001c0001t0017g0078a0001c0001t0018g0128others(1): Show | 4 | 180 | 0.0222 | -14 | c.71- others(31): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 2/7 | chr11 | TogoVar | ||||||
FAM168A_chr11_73395487_73603112 | 73484505 | GAGATATA others(7): Show |
G | intron_variant | MODIFIER | HG01884.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0004a0001c0001t0011a0001c0001t0014others(7): Show | a0001c0001t0004g0137a0001c0001t0004g0139a0001c0001t0004g0140others(19): Show | 22 | 180 | 0.1222 | -14 | c.-18 others(33): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | TogoVar | ||||||
FAM168A_chr11_73395487_73603112 | 73484682 | CTATAGAT others(7): Show |
C | intron_variant | MODIFIER | HG01109.hp2 | a0002 | a0002c0005 | a0002c0005t0001 | a0002c0005t0001g0055 | 1 | 180 | 0.0056 | -14 | c.-18 others(33): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | TogoVar | ||||||
FAM168A_chr11_73395487_73603112 | 73544895 | AATATATT others(7): Show |
A | intron_variant | MODIFIER | HG02083.hp1 HG02083.hp2 |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0021 | a0001c0002t0001g0053a0001c0002t0021g0104 | 2 | 180 | 0.0111 | -14 | c.-19 others(33): Show |
FAM168A | ENSG00000054965.11 | transcript | ENST00000356467.5 | protein_coding | 1/7 | chr11 | TogoVar | ||||||
FAM169A_chr5_74772574_74871387 | 74857572 | GAAAAAAA others(7): Show |
G | intron_variant | MODIFIER | HG01109.hp2 HG02015.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004 | a0001c0001t0003g0079a0001c0001t0004g0049 | 2 | 308 | 0.0065 | -14 | c.-4+ others(29): Show |
FAM169A | ENSG00000198780.13 | transcript | ENST00000687041.1 | protein_coding | 1/12 | chr5 | TogoVar | ||||||
FAM170A_chr5_119624558_119640822 | 119631401 | CTGTGTGT others(7): Show |
C | intron_variant | MODIFIER | HG03516.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0069 | 1 | 436 | 0.0023 | -14 | c.71- others(29): Show |
FAM170A | ENSG00000164334.16 | transcript | ENST00000695508.1 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
FAM171A1_chr10_15206643_15376289 | 15211314 | CTTTTTTT others(7): Show |
C | downstream_gene_variant | MODIFIER | NA19043.hp1 NA19070.hp2 NA19081.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0009 | a0001c0001t0002g0103a0001c0001t0002g0105a0001c0001t0003g0243others(1): Show | 4 | 303 | 0.0132 | -14 | c.*15 others(25): Show |
FAM171A1 | ENSG00000148468.17 | transcript | ENST00000378116.9 | protein_coding | 328 | chr10 | TogoVar | ||||||
FAM171A1_chr10_15206643_15376289 | 15312673 | GTTTTTTT others(7): Show |
G | intron_variant | MODIFIER | HG02572.hp2 HG02723.hp2 NA19011.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0005 | a0001c0001t0001g0228a0001c0001t0003g0285a0001c0001t0005g0129 | 3 | 303 | 0.0099 | -14 | c.98- others(31): Show |
FAM171A1 | ENSG00000148468.17 | transcript | ENST00000378116.9 | protein_coding | 1/7 | chr10 | TogoVar | ||||||
FAM171A1_chr10_15206643_15376289 | 15375715 | CTTTTTTT others(7): Show |
C | upstream_gene_variant | MODIFIER | NA18939.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0230 | 1 | 303 | 0.0033 | -14 | c.-46 others(25): Show |
FAM171A1 | ENSG00000148468.17 | transcript | ENST00000378116.9 | protein_coding | 4427 | chr10 | TogoVar | ||||||
FAM171A2_chr17_44348215_44368853 | 44368138 | ATATATAT others(7): Show |
A | upstream_gene_variant | MODIFIER | HG02273.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 416 | 0.0024 | -14 | c.-44 others(25): Show |
FAM171A2 | ENSG00000161682.15 | transcript | ENST00000293443.12 | protein_coding | 4286 | chr17 | TogoVar | ||||||
FAM171B_chr2_186689060_186770959 | 186693145 | TCACACAC others(7): Show |
T | upstream_gene_variant | MODIFIER | HG02738.hp1 HG03688.hp2 |
a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0049a0001c0005t0001g0070 | 2 | 332 | 0.0060 | -14 | c.-10 others(25): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 914 | chr2 | TogoVar | ||||||
FAM171B_chr2_186689060_186770959 | 186694748 | AACACACA others(7): Show |
A | intron_variant | MODIFIER | NA18954.hp2 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0291 | 1 | 332 | 0.0030 | -14 | c.238 others(29): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
FAM171B_chr2_186689060_186770959 | 186756170 | TATTTGTT others(7): Show |
T | intron_variant | MODIFIER | HG01243.hp2 HG01256.hp1 HG01258.hp1 others(1): Show |
a0001a0005 | a0001c0005a0005c0024 | a0001c0005t0001a0005c0024t0001 | a0001c0005t0001g0073a0001c0005t0001g0078a0001c0005t0001g0096others(1): Show | 4 | 332 | 0.0121 | -14 | c.101 others(33): Show |
FAM171B | ENSG00000144369.14 | transcript | ENST00000304698.10 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
FAM172A_chr5_93612725_94116663 | 93653511 | CAAAAAAA others(7): Show |
C | intron_variant | MODIFIER | NA19064.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0038 | 1 | 126 | 0.0079 | -14 | c.110 others(35): Show |
FAM172A | ENSG00000113391.19 | transcript | ENST00000395965.8 | protein_coding | 10/10 | chr5 | TogoVar | ||||||
FAM172A_chr5_93612725_94116663 | 93767993 | CAAAAAAA others(7): Show |
C | intron_variant | MODIFIER | HG02055.hp2 HG02258.hp2 HG02717.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0024a0001c0001t0002g0118a0001c0001t0002g0119others(2): Show | 5 | 126 | 0.0397 | -14 | c.110 others(33): Show |
FAM172A | ENSG00000113391.19 | transcript | ENST00000395965.8 | protein_coding | 10/10 | chr5 | TogoVar | ||||||
FAM172A_chr5_93612725_94116663 | 93800381 | TCACACAC others(7): Show |
T | intron_variant | MODIFIER | HG00642.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0065 | 1 | 126 | 0.0079 | -14 | c.907 others(33): Show |
FAM172A | ENSG00000113391.19 | transcript | ENST00000395965.8 | protein_coding | 8/10 | chr5 | TogoVar | ||||||
FAM172A_chr5_93612725_94116663 | 93983170 | GGTGTGTG others(7): Show |
G | intron_variant | MODIFIER | HG00323.hp2 HG00544.hp2 HG01070.hp1 others(27): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(5): Show | a0001c0001t0001g0028a0001c0001t0001g0042a0001c0001t0001g0066others(27): Show | 30 | 126 | 0.2381 | -14 | c.310 others(33): Show |
FAM172A | ENSG00000113391.19 | transcript | ENST00000395965.8 | protein_coding | 4/10 | chr5 | TogoVar | ||||||
FAM172A_chr5_93612725_94116663 | 94004538 | TGCCACTG others(7): Show |
T | intron_variant | MODIFIER | NA19056.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0091 | 1 | 126 | 0.0079 | -14 | c.310 others(33): Show |
FAM172A | ENSG00000113391.19 | transcript | ENST00000395965.8 | protein_coding | 4/10 | chr5 | TogoVar | ||||||
FAM174A_chr5_100530374_100591741 | 100544348 | ATACCCCT others(7): Show |
A | intron_variant | MODIFIER | HG01255.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0246 | 1 | 298 | 0.0034 | -14 | c.434 others(31): Show |
FAM174A | ENSG00000174132.9 | transcript | ENST00000312637.5 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
FAM174B_chr15_92612448_92660775 | 92630901 | CATATTAT others(7): Show |
C | intron_variant | MODIFIER | HG01975.hp2 HG02451.hp2 |
a0001 | a0001c0001 | a0001c0001t0012a0001c0001t0033 | a0001c0001t0012g0350a0001c0001t0033g0342 | 2 | 394 | 0.0051 | -14 | c.345 others(29): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | TogoVar | ||||||
FAM174B_chr15_92612448_92660775 | 92630936 | CATATTAT others(7): Show |
C | intron_variant | MODIFIER | HG02683.hp2 | a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0352 | 1 | 394 | 0.0025 | -14 | c.345 others(29): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | TogoVar | ||||||
FAM174B_chr15_92612448_92660775 | 92630971 | CATATTAT others(7): Show |
C | intron_variant | MODIFIER | HG03942.hp1 | a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0351 | 1 | 394 | 0.0025 | -14 | c.345 others(29): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | TogoVar | ||||||
FAM174B_chr15_92612448_92660775 | 92635159 | CCACACAC others(7): Show |
C | intron_variant | MODIFIER | HG01258.hp2 HG02486.hp1 HG02717.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(3): Show | a0001c0001t0001g0027a0001c0001t0005g0258a0001c0001t0009g0029others(3): Show | 6 | 394 | 0.0152 | -14 | c.345 others(31): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | TogoVar | ||||||
FAM174B_chr15_92612448_92660775 | 92640551 | CAAAAAAA others(7): Show |
C | intron_variant | MODIFIER | HG00642.hp2 HG02486.hp2 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0052 | a0001c0001t0004g0316a0001c0001t0052g0317 | 2 | 394 | 0.0051 | -14 | c.345 others(33): Show |
FAM174B | ENSG00000185442.13 | transcript | ENST00000327355.6 | protein_coding | 1/2 | chr15 | TogoVar | ||||||
FAM177A1_chr14_35041272_35088378 | 35061358 | AGGTTTTG others(7): Show |
A | intron_variant | MODIFIER | NA19006.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0130 | 1 | 370 | 0.0027 | -14 | c.339 others(31): Show |
FAM177A1 | ENSG00000151327.14 | transcript | ENST00000280987.9 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
FAM178B_chr2_96870885_96991580 | 96905814 | GTGTGTAT others(7): Show |
G | intron_variant | MODIFIER | HG02027.hp1 HG02071.hp2 |
a0008 | a0008c0014 | a0008c0014t0001 | a0008c0014t0001g0228a0008c0014t0001g0231 | 2 | 250 | 0.0080 | -14 | c.156 others(33): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | TogoVar | ||||||
FAM178B_chr2_96870885_96991580 | 96905816 | GTGTATAT others(7): Show |
G | intron_variant | MODIFIER | HG02027.hp2 | a0002 | a0002c0008 | a0002c0008t0001 | a0002c0008t0001g0234 | 1 | 250 | 0.0040 | -14 | c.156 others(33): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | TogoVar | ||||||
FAM178B_chr2_96870885_96991580 | 96905850 | ATATATAT others(7): Show |
A | intron_variant | MODIFIER | HG01257.hp2 HG02300.hp2 |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0151a0002c0002t0001g0166 | 2 | 250 | 0.0080 | -14 | c.156 others(33): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 12/16 | chr2 | TogoVar | ||||||
FAM178B_chr2_96870885_96991580 | 96958697 | TAAAAAAA others(7): Show |
T | intron_variant | MODIFIER | HG02895.hp2 HG02897.hp1 HG02976.hp2 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0008a0001c0001t0001g0085a0001c0001t0001g0103others(1): Show | 4 | 250 | 0.0160 | -14 | c.887 others(31): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 6/16 | chr2 | TogoVar | ||||||
FAM178B_chr2_96870885_96991580 | 96987178 | CAAAAAAA others(7): Show |
C | upstream_gene_variant | MODIFIER | HG01175.hp1 HG02055.hp1 HG02559.hp2 |
a0001a0004 | a0001c0003a0004c0004 | a0001c0003t0001a0004c0004t0001 | a0001c0003t0001g0223a0004c0004t0001g0128a0004c0004t0001g0130 | 3 | 250 | 0.0120 | -14 | c.-87 others(23): Show |
FAM178B | ENSG00000168754.15 | transcript | ENST00000490605.3 | protein_coding | 599 | chr2 | TogoVar |