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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
CRTC3_chr15_90524923_90650345 | 90647402 | C | CCCTCCTC others(4667): Show |
downstream_gene_variant | MODIFIER | HG04115.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0157 | 1 | 276 | 0.0036 | 4674 | c.*52 others(4685): Show |
CRTC3 | ENSG00000140577.17 | transcript | ENST00000268184.11 | protein_coding | 2058 | chr15 | TogoVar | |||||||
FOXK2_chr17_82514732_82609602 | 82586256 | G | GGGGGGGA others(4667): Show |
intron_variant | MODIFIER | HG03831.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0278 | 1 | 308 | 0.0033 | 4674 | c.157 others(4689): Show |
FOXK2 | ENSG00000141568.21 | transcript | ENST00000335255.10 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
FAM227A_chr22_38573118_38661392 | 38644446 | A | ACTATGCT others(4668): Show |
intron_variant | MODIFIER | HG03195.hp1 | a0001 | a0001c0001 | a0001c0001t0057 | a0001c0001t0057g0278 | 1 | 328 | 0.0031 | 4675 | c.225 others(4692): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | TogoVar | |||||||
FAM227A_chr22_38573118_38661392 | 38644446 | A | ACTATGCT others(4668): Show |
intron_variant | MODIFIER | HG01993.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0260 | 1 | 328 | 0.0031 | 4675 | c.225 others(4692): Show |
FAM227A | ENSG00000184949.18 | transcript | ENST00000535113.7 | protein_coding | 3/16 | chr22 | TogoVar | |||||||
MLPH_chr2_237482251_237560322 | 237544145 | T | TGGGGACA others(4668): Show |
intron_variant | MODIFIER | HG02165.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0250 | 1 | 286 | 0.0035 | 4675 | c.153 others(4694): Show |
MLPH | ENSG00000115648.14 | transcript | ENST00000264605.8 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(4672): Show |
upstream_gene_variant | MODIFIER | HG02809.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0098 | 1 | 251 | 0.0040 | 4679 | c.-45 others(4688): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
BTNL9_chr5_181035266_181066521 | 181045891 | G | GACACCTC others(4673): Show |
intron_variant | MODIFIER | HG01070.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0242 | 1 | 390 | 0.0026 | 4680 | c.109 others(4695): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
BTNL9_chr5_181035266_181066521 | 181046000 | C | CCCCAGCC others(4673): Show |
intron_variant | MODIFIER | HG01952.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0241 | 1 | 390 | 0.0026 | 4680 | c.109 others(4695): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
MEGF6_chr1_3482951_3616508 | 3502017 | G | GCCTCACA others(4673): Show |
intron_variant | MODIFIER | NA20300.hp2 | a0097 | a0097c0069 | a0097c0069t0004 | a0097c0069t0004g0249 | 1 | 292 | 0.0034 | 4680 | c.218 others(4695): Show |
MEGF6 | ENSG00000162591.17 | transcript | ENST00000356575.9 | protein_coding | 17/36 | chr1 | TogoVar | |||||||
RPTOR_chr17_80539838_80971368 | 80744785 | T | TAGCACTG others(4673): Show |
intron_variant | MODIFIER | HG00621.hp2 | a0001 | a0001c0018 | a0001c0018t0009 | a0001c0018t0009g0066 | 1 | 196 | 0.0051 | 4680 | c.655 others(4697): Show |
RPTOR | ENSG00000141564.16 | transcript | ENST00000306801.8 | protein_coding | 5/33 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
SERINC2_chr1_31408213_31439678 | 31431966 | A | ATAGGGTG others(4673): Show |
intron_variant | MODIFIER | NA18991.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0301 | 1 | 376 | 0.0027 | 4680 | c.101 others(4697): Show |
SERINC2 | ENSG00000168528.12 | transcript | ENST00000373709.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
BTNL9_chr5_181035266_181066521 | 181046000 | C | CCCCAGCC others(4674): Show |
intron_variant | MODIFIER | HG01891.hp2 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0156 | 1 | 390 | 0.0026 | 4681 | c.109 others(4696): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
DOCK1_chr10_126900428_127457516 | 126947680 | A | ATGGTGGT others(4674): Show |
intron_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0065 | 1 | 136 | 0.0074 | 4681 | c.47- others(4698): Show |
DOCK1 | ENSG00000150760.13 | transcript | ENST00000623213.2 | protein_coding | 1/51 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
MYO16_chr13_108624611_109213005 | 108690374 | G | GGAAGGGC others(4674): Show |
intron_variant | MODIFIER | HG02895.hp1 HG02897.hp1 |
a0001 | a0001c0010 | a0001c0010t0001 | a0001c0010t0001g0129 a0001c0010t0001g0130 |
2 | 152 | 0.0132 | 4681 | c.293 others(4700): Show |
MYO16 | ENSG00000041515.16 | transcript | ENST00000457511.7 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
MYO16_chr13_108624611_109213005 | 108690374 | G | GGAAGGGC others(4674): Show |
intron_variant | MODIFIER | HG00738.hp1 HG01081.hp1 HG01175.hp1 others(14): Show |
a0001a0002a0003others(5): Show | a0001c0002a0001c0007a0002c0001others(9): Show | a0001c0002t0015a0001c0002t0021a0001c0007t0001others(13): Show | a0001c0002t0015g0038 a0001c0002t0021g0032 a0001c0007t0001g0010 others(14): Show |
17 | 152 | 0.1118 | 4681 | c.293 others(4700): Show |
MYO16 | ENSG00000041515.16 | transcript | ENST00000457511.7 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
MYO16_chr13_108624611_109213005 | 108690374 | G | GGAAGGGC others(4674): Show |
intron_variant | MODIFIER | HG03471.hp1 | a0008 | a0008c0006 | a0008c0006t0004 | a0008c0006t0004g0138 | 1 | 152 | 0.0066 | 4681 | c.293 others(4700): Show |
MYO16 | ENSG00000041515.16 | transcript | ENST00000457511.7 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
MYO16_chr13_108624611_109213005 | 108690374 | G | GGAAGGGC others(4674): Show |
intron_variant | MODIFIER | HG01099.hp1 HG01952.hp2 HG01978.hp2 others(5): Show |
a0001a0002a0004others(3): Show | a0001c0002a0002c0001a0004c0003others(3): Show | a0001c0002t0002a0002c0001t0019a0004c0003t0001others(4): Show | a0001c0002t0002g0027 a0002c0001t0019g0125 a0004c0003t0001g0087 others(5): Show |
8 | 152 | 0.0526 | 4681 | c.293 others(4700): Show |
MYO16 | ENSG00000041515.16 | transcript | ENST00000457511.7 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
MYO16_chr13_108624611_109213005 | 108690374 | G | GGAAGGGC others(4674): Show |
intron_variant | MODIFIER | HG01943.hp2 | a0002 | a0002c0001 | a0002c0001t0001 | a0002c0001t0001g0112 | 1 | 152 | 0.0066 | 4681 | c.293 others(4700): Show |
MYO16 | ENSG00000041515.16 | transcript | ENST00000457511.7 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
MYO16_chr13_108624611_109213005 | 108690374 | G | GGAAGGGC others(4674): Show |
intron_variant | MODIFIER | NA19066.hp1 | a0010 | a0010c0012 | a0010c0012t0001 | a0010c0012t0001g0021 | 1 | 152 | 0.0066 | 4681 | c.293 others(4700): Show |
MYO16 | ENSG00000041515.16 | transcript | ENST00000457511.7 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
MYO16_chr13_108624611_109213005 | 108690374 | G | GGAAGGGC others(4674): Show |
intron_variant | MODIFIER | NA18950.hp2 | a0004 | a0004c0026 | a0004c0026t0002 | a0004c0026t0002g0127 | 1 | 152 | 0.0066 | 4681 | c.293 others(4700): Show |
MYO16 | ENSG00000041515.16 | transcript | ENST00000457511.7 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
MYO16_chr13_108624611_109213005 | 108690374 | G | GGAAGGGC others(4675): Show |
intron_variant | MODIFIER | HG00099.hp1 | a0002 | a0002c0053 | a0002c0053t0009 | a0002c0053t0009g0116 | 1 | 152 | 0.0066 | 4682 | c.293 others(4701): Show |
MYO16 | ENSG00000041515.16 | transcript | ENST00000457511.7 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
MYO16_chr13_108624611_109213005 | 108690374 | G | GGAAGGGC others(4675): Show |
intron_variant | MODIFIER | HG03195.hp2 NA20300.hp2 |
a0003a0011 | a0003c0060a0011c0018 | a0003c0060t0004a0011c0018t0001 | a0003c0060t0004g0074 a0011c0018t0001g0152 |
2 | 152 | 0.0132 | 4682 | c.293 others(4701): Show |
MYO16 | ENSG00000041515.16 | transcript | ENST00000457511.7 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
RBFOX2_chr22_35733736_36033824 | 35735274 | C | CCTCCTGC others(4675): Show |
downstream_gene_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0021 | 1 | 120 | 0.0083 | 4682 | c.*89 others(4693): Show |
RBFOX2 | ENSG00000100320.24 | transcript | ENST00000695854.1 | protein_coding | 3461 | chr22 | TogoVar | |||||||
TPO_chr2_1408463_1548673 | 1525660 | C | CCCCCCCA others(4675): Show |
intron_variant | MODIFIER | NA19088.hp2 | a0003 | a0003c0006 | a0003c0006t0004 | a0003c0006t0004g0100 | 1 | 130 | 0.0077 | 4682 | c.261 others(4701): Show |
TPO | ENSG00000115705.22 | transcript | ENST00000329066.9 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ABR_chr17_998519_1184981 | 1065147 | C | TGTGAACT others(4676): Show |
intron_variant | MODIFIER | HG01496.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0026 | 1 | 337 | 0.0030 | 4683 | c.118 others(4702): Show |
ABR | ENSG00000159842.16 | transcript | ENST00000302538.10 | protein_coding | 10/22 | chr17 | TogoVar | |||||||
MYO16_chr13_108624611_109213005 | 108690374 | G | GGAAGGGC others(4676): Show |
intron_variant | MODIFIER | HG00642.hp1 HG01952.hp1 NA19057.hp1 |
a0002a0003 | a0002c0001a0003c0004a0003c0044 | a0002c0001t0003a0003c0004t0002a0003c0044t0002 | a0002c0001t0003g0105 a0003c0004t0002g0108 a0003c0044t0002g0148 |
3 | 152 | 0.0197 | 4683 | c.293 others(4702): Show |
MYO16 | ENSG00000041515.16 | transcript | ENST00000457511.7 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
LRRC27_chr10_132327193_132386508 | 132364375 | A | ACGCTTAC others(4677): Show |
intron_variant | MODIFIER | NA18747.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0166 | 1 | 290 | 0.0035 | 4684 | c.129 others(4703): Show |
LRRC27 | ENSG00000148814.18 | transcript | ENST00000368614.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr10 | TogoVar | ||||||
PIEZO1_chr16_88710338_88790220 | 88731922 | A | AGAGGGCG others(4677): Show |
intron_variant | MODIFIER | HG01943.hp2 | a0005 | a0005c0015 | a0005c0015t0001 | a0005c0015t0001g0048 | 1 | 282 | 0.0036 | 4684 | c.299 others(4699): Show |
PIEZO1 | ENSG00000103335.22 | transcript | ENST00000301015.14 | protein_coding | 21/50 | chr16 | TogoVar | |||||||
NBPF14_chr1_148526385_148601011 | 148538215 | C | CACACACA others(4681): Show |
intron_variant | MODIFIER | HG02056.hp2 | a0065 | a0065c0070 | a0065c0070t0001 | a0065c0070t0001g0051 | 1 | 222 | 0.0045 | 4688 | c.793 others(4705): Show |
NBPF14 | ENSG00000270629.7 | transcript | ENST00000619423.4 | protein_coding | 64/70 | chr1 | TogoVar | |||||||
NBPF14_chr1_148526385_148601011 | 148538215 | C | CACACACA others(4681): Show |
intron_variant | MODIFIER | NA18952.hp1 | a0017 | a0017c0035 | a0017c0035t0001 | a0017c0035t0001g0017 | 1 | 222 | 0.0045 | 4688 | c.793 others(4705): Show |
NBPF14 | ENSG00000270629.7 | transcript | ENST00000619423.4 | protein_coding | 64/70 | chr1 | TogoVar | |||||||
CLPTM1L_chr5_1312752_1350099 | 1333664 | T | TGAGGATA others(4682): Show |
intron_variant | MODIFIER | HG03942.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0174 | 1 | 370 | 0.0027 | 4689 | c.891 others(4704): Show |
CLPTM1L | ENSG00000049656.14 | transcript | ENST00000320895.10 | protein_coding | 7/16 | chr5 | TogoVar | |||||||
AZU1_chr19_822837_837018 | 834154 | T | CGTCTCAA others(4683): Show |
downstream_gene_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0042 | 1 | 391 | 0.0026 | 4690 | c.*22 others(4701): Show |
AZU1 | ENSG00000172232.10 | transcript | ENST00000233997.4 | protein_coding | 2136 | chr19 | TogoVar | |||||||
CNOT3_chr19_54132762_54160681 | 54133829 | C | CTCCCTCC others(4683): Show |
upstream_gene_variant | MODIFIER | HG02132.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0001 | 1 | 223 | 0.0045 | 4690 | c.-42 others(4701): Show |
CNOT3 | ENSG00000088038.20 | transcript | ENST00000221232.11 | protein_coding | 3932 | chr19 | TogoVar | |||||||
MYO16_chr13_108624611_109213005 | 108690374 | G | GGAAGGGC others(4683): Show |
intron_variant | MODIFIER | NA18522.hp2 NA18906.hp1 |
a0001a0014 | a0001c0008a0014c0054 | a0001c0008t0004a0014c0054t0001 | a0001c0008t0004g0019 a0014c0054t0001g0020 |
2 | 152 | 0.0132 | 4690 | c.293 others(4709): Show |
MYO16 | ENSG00000041515.16 | transcript | ENST00000457511.7 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
NBPF14_chr1_148526385_148601011 | 148571250 | C | CACACACA others(4683): Show |
intron_variant | MODIFIER | HG00621.hp1 | a0021 | a0021c0058 | a0021c0058t0011 | a0021c0058t0011g0102 | 1 | 222 | 0.0045 | 4690 | c.281 others(4707): Show |
NBPF14 | ENSG00000270629.7 | transcript | ENST00000619423.4 | protein_coding | 22/70 | chr1 | TogoVar | |||||||
PIEZO1_chr16_88710338_88790220 | 88731922 | A | AGAGGGCG others(4683): Show |
intron_variant | MODIFIER | HG03516.hp2 | a0003 | a0003c0005 | a0003c0005t0010 | a0003c0005t0010g0002 | 1 | 282 | 0.0036 | 4690 | c.299 others(4705): Show |
PIEZO1 | ENSG00000103335.22 | transcript | ENST00000301015.14 | protein_coding | 21/50 | chr16 | TogoVar | |||||||
SNTG2_chr2_945849_1372613 | 1222982 | T | TGCAGTGA others(4683): Show |
intron_variant | MODIFIER | NA18522.hp2 | a0003 | a0003c0008 | a0003c0008t0001 | a0003c0008t0001g0106 | 1 | 190 | 0.0053 | 4690 | c.719 others(4709): Show |
SNTG2 | ENSG00000172554.12 | transcript | ENST00000308624.10 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
MEIS3_chr19_47398124_47424527 | 47419530 | T | TCTCTGTG others(4684): Show |
upstream_gene_variant | MODIFIER | HG01074.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0024 | 1 | 251 | 0.0040 | 4691 | c.-45 others(4700): Show |
MEIS3 | ENSG00000105419.18 | transcript | ENST00000558555.6 | protein_coding | 4 | chr19 | TogoVar | |||||||
MYO16_chr13_108624611_109213005 | 108690374 | G | GGAAGGGC others(4684): Show |
intron_variant | MODIFIER | HG02572.hp1 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0018 | 1 | 152 | 0.0066 | 4691 | c.293 others(4710): Show |
MYO16 | ENSG00000041515.16 | transcript | ENST00000457511.7 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
BRF1_chr14_105204286_105306001 | 105240577 | T | TGTGGCAC others(4685): Show |
intron_variant | MODIFIER | HG02630.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005 | 1 | 72 | 0.0139 | 4692 | c.694 others(4707): Show |
BRF1 | ENSG00000185024.18 | transcript | ENST00000547530.7 | protein_coding | 6/17 | chr14 | TogoVar | |||||||
DLEC1_chr3_38034208_38129025 | 38084579 | G | GGGGGGTG others(4685): Show |
intron_variant | MODIFIER | HG02647.hp1 | a0015 | a0015c0062 | a0015c0062t0002 | a0015c0062t0002g0134 | 1 | 298 | 0.0034 | 4692 | c.126 others(4709): Show |
DLEC1 | ENSG00000008226.20 | transcript | ENST00000308059.11 | protein_coding | 7/36 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
MYO16_chr13_108624611_109213005 | 108690374 | G | GGAAGGGC others(4685): Show |
intron_variant | MODIFIER | HG02976.hp1 | a0002 | a0002c0001 | a0002c0001t0004 | a0002c0001t0004g0017 | 1 | 152 | 0.0066 | 4692 | c.293 others(4711): Show |
MYO16 | ENSG00000041515.16 | transcript | ENST00000457511.7 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar | ||||||
PHRF1_chr11_571470_617222 | 585474 | T | TTGAGGTA others(4685): Show |
intron_variant | MODIFIER | HG01168.hp2 | a0005 | a0005c0007 | a0005c0007t0001 | a0005c0007t0001g0179 | 1 | 279 | 0.0036 | 4692 | c.215 others(4709): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PHRF1_chr11_571470_617222 | 585474 | T | TTGAGGTA others(4685): Show |
intron_variant | MODIFIER | HG02683.hp1 | a0005 | a0005c0007 | a0005c0007t0001 | a0005c0007t0001g0089 | 1 | 279 | 0.0036 | 4692 | c.215 others(4709): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PHRF1_chr11_571470_617222 | 585658 | T | TTGAGGTA others(4685): Show |
intron_variant | MODIFIER | HG02080.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0157 | 1 | 279 | 0.0036 | 4692 | c.215 others(4709): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PHRF1_chr11_571470_617222 | 585658 | T | TTGAGGTA others(4685): Show |
intron_variant | MODIFIER | HG00438.hp2 NA18964.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062 a0001c0001t0001g0076 |
2 | 279 | 0.0072 | 4692 | c.215 others(4709): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PHRF1_chr11_571470_617222 | 585658 | T | TTGAGGTA others(4685): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0011 | a0011c0017 | a0011c0017t0001 | a0011c0017t0001g0103 | 1 | 279 | 0.0036 | 4692 | c.215 others(4709): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PHRF1_chr11_571470_617222 | 585658 | T | TTGAGGTA others(4685): Show |
intron_variant | MODIFIER | HG01106.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0142 | 1 | 279 | 0.0036 | 4692 | c.215 others(4709): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
PHRF1_chr11_571470_617222 | 585658 | T | TTGAGGTA others(4685): Show |
intron_variant | MODIFIER | HG03492.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0200 | 1 | 279 | 0.0036 | 4692 | c.215 others(4709): Show |
PHRF1 | ENSG00000070047.13 | transcript | ENST00000264555.10 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
MYO16_chr13_108624611_109213005 | 108690374 | G | GGAAGGGC others(4688): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0001 | 1 | 152 | 0.0066 | 4695 | c.293 others(4714): Show |
MYO16 | ENSG00000041515.16 | transcript | ENST00000457511.7 | protein_coding | 2/34 | INFO_REALIGN_3_PRIME | chr13 | TogoVar |