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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
AAMDC_chr11_77816144_77877352 | 77866931 | C | T | intron_variant | MODIFIER | NA19011.hp2 NA19063.hp1 NA19090.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0118a0001c0001t0001g0128a0001c0001t0001g0154 | 3 | 382 | 0.0079 | 0 | c.133 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77867187 | G | A | intron_variant | MODIFIER | HG02074.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0198 | 1 | 382 | 0.0026 | 0 | c.133 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77867312 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
a0001a0002 | a0001c0002a0002c0003a0002c0004 | a0001c0002t0001a0001c0002t0002a0002c0003t0001others(1): Show | a0001c0002t0001g0009a0001c0002t0001g0012a0001c0002t0001g0019others(153): Show | 160 | 382 | 0.4189 | -1 | c.133 others(9): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
AAMDC_chr11_77816144_77877352 | 77867339 | C | T | intron_variant | MODIFIER | NA18954.hp2 NA18988.hp2 NA19079.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0324a0001c0001t0001g0325a0001c0001t0001g0327 | 3 | 382 | 0.0079 | 0 | c.133 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77867494 | T | C | intron_variant | MODIFIER | HG02055.hp2 HG02109.hp2 HG02602.hp2 others(17): Show |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0006a0001c0002t0002g0208a0001c0002t0002g0218others(16): Show | 20 | 382 | 0.0524 | 0 | c.133 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77867584 | G | A | intron_variant | MODIFIER | HG02922.hp1 HG03209.hp1 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0351a0001c0002t0002g0353 | 2 | 382 | 0.0052 | 0 | c.133 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77867915 | A | G | intron_variant | MODIFIER | HG01123.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0187 | 1 | 382 | 0.0026 | 0 | c.133 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77867960 | T | C | intron_variant | MODIFIER | NA19088.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0161 | 1 | 382 | 0.0026 | 0 | c.133 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77868058 | C | CT | intron_variant | MODIFIER | HG00140.hp2 HG00673.hp2 HG00733.hp2 others(78): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0001g0158a0001c0001t0001g0190a0001c0001t0001g0308others(76): Show | 81 | 382 | 0.2120 | 1 | c.133 others(9): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
AAMDC_chr11_77816144_77877352 | 77868058 | C | CTT | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(75): Show |
a0001a0002 | a0001c0002a0002c0003a0002c0004 | a0001c0002t0001a0001c0002t0002a0002c0003t0001others(1): Show | a0001c0002t0001g0012a0001c0002t0001g0019a0001c0002t0001g0020others(73): Show | 78 | 382 | 0.2042 | 2 | c.133 others(19): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
AAMDC_chr11_77816144_77877352 | 77868087 | G | A | intron_variant | MODIFIER | HG03490.hp1 HG03492.hp1 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0261a0001c0002t0002g0264 | 2 | 382 | 0.0052 | 0 | c.133 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77868132 | T | C | intron_variant | MODIFIER | NA19240.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0024 | 1 | 382 | 0.0026 | 0 | c.133 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77868181 | G | A | intron_variant | MODIFIER | NA18955.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0370 | 1 | 382 | 0.0026 | 0 | c.133 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77868343 | C | T | intron_variant | MODIFIER | HG00140.hp2 HG01123.hp1 HG01255.hp1 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0265a0001c0002t0002g0268a0001c0002t0002g0269 | 3 | 382 | 0.0079 | 0 | c.133 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77868357 | C | CT | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(82): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(2): Show | a0001c0001t0001g0005a0001c0001t0001g0106a0001c0001t0001g0155others(79): Show | 85 | 382 | 0.2225 | 1 | c.133 others(9): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
AAMDC_chr11_77816144_77877352 | 77868399 | C | T | intron_variant | MODIFIER | HG02602.hp2 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0232 | 1 | 382 | 0.0026 | 0 | c.133 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77868507 | C | T | intron_variant | MODIFIER | HG02895.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0009 | 1 | 382 | 0.0026 | 0 | c.133 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77868695 | G | C | intron_variant | MODIFIER | HG02451.hp2 HG02818.hp2 HG03195.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005a0001c0001t0001g0106a0001c0001t0001g0200others(1): Show | 5 | 382 | 0.0131 | 0 | c.133 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77868698 | GTTT | G | intron_variant | MODIFIER | HG01074.hp2 HG01243.hp2 HG01496.hp2 others(12): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0002 | a0001c0002t0001g0022a0001c0002t0001g0023a0001c0002t0001g0024others(12): Show | 15 | 382 | 0.0393 | -3 | c.133 others(20): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
AAMDC_chr11_77816144_77877352 | 77868701 | T | G | intron_variant | MODIFIER | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(66): Show |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0006a0001c0002t0002g0007a0001c0002t0002g0208others(64): Show | 69 | 382 | 0.1806 | 0 | c.133 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77868807 | C | T | intron_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0105 | 1 | 382 | 0.0026 | 0 | c.133 others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77868994 | T | C | intron_variant | MODIFIER | HG00408.hp2 HG00609.hp2 HG01123.hp2 others(18): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(18): Show | 21 | 382 | 0.0550 | 0 | c.133 others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77869100 | C | T | intron_variant | MODIFIER | NA19078.hp1 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0031 | 1 | 382 | 0.0026 | 0 | c.133 others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77869123 | C | A | intron_variant | MODIFIER | NA18971.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0263 | 1 | 382 | 0.0026 | 0 | c.133 others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77869169 | T | C | intron_variant | MODIFIER | HG02615.hp1 | a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0074 | 1 | 382 | 0.0026 | 0 | c.133 others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77869194 | AT | A | intron_variant | MODIFIER | HG01884.hp1 HG02145.hp1 HG02280.hp2 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0019a0001c0002t0001g0020a0001c0002t0001g0021 | 3 | 382 | 0.0079 | -1 | c.133 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
AAMDC_chr11_77816144_77877352 | 77869302 | A | ATC | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(38): Show |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0007a0001c0002t0002g0219a0001c0002t0002g0224others(37): Show | 41 | 382 | 0.1073 | 2 | c.133 others(17): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
AAMDC_chr11_77816144_77877352 | 77869305 | T | A | intron_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0192 | 1 | 382 | 0.0026 | 0 | c.133 others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77869306 | C | CTT | intron_variant | MODIFIER | HG00639.hp2 HG01496.hp2 HG02055.hp2 others(22): Show |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0006a0001c0002t0002g0109a0001c0002t0002g0207others(21): Show | 25 | 382 | 0.0655 | 2 | c.133 others(17): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
AAMDC_chr11_77816144_77877352 | 77869306 | C | CTTT | intron_variant | MODIFIER | HG02622.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0218a0001c0002t0002g0226a0001c0002t0002g0228others(3): Show | 6 | 382 | 0.0157 | 3 | c.133 others(18): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
AAMDC_chr11_77816144_77877352 | 77869307 | T | TC | intron_variant | MODIFIER | HG01167.hp2 HG01168.hp2 HG03491.hp2 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0255a0001c0002t0002g0282a0001c0002t0002g0349 | 3 | 382 | 0.0079 | 1 | c.133 others(16): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77869308 | T | C | intron_variant | MODIFIER | HG00099.hp1 HG00639.hp1 HG01516.hp2 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0247a0001c0002t0002g0250a0001c0002t0002g0348 | 3 | 382 | 0.0079 | 0 | c.133 others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77869312 | C | CT | intron_variant | MODIFIER | HG00597.hp2 HG00735.hp1 HG01074.hp1 others(33): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0002t0001a0002c0003t0001others(1): Show | a0001c0001t0001g0005a0001c0001t0001g0102a0001c0001t0001g0106others(32): Show | 36 | 382 | 0.0942 | 1 | c.133 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
AAMDC_chr11_77816144_77877352 | 77869312 | C | CTT | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
a0001a0002 | a0001c0002a0002c0003a0002c0004 | a0001c0002t0001a0002c0003t0001a0002c0004t0001 | a0001c0002t0001g0012a0001c0002t0001g0019a0001c0002t0001g0020others(62): Show | 67 | 382 | 0.1754 | 2 | c.133 others(17): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
AAMDC_chr11_77816144_77877352 | 77869312 | C | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(74): Show |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0006a0001c0002t0002g0007a0001c0002t0002g0109others(72): Show | 77 | 382 | 0.2016 | 0 | c.133 others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77869312 | CT | C | intron_variant | MODIFIER | HG01167.hp1 HG01256.hp1 HG01515.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0148a0001c0001t0001g0321a0001c0001t0001g0324others(4): Show | 7 | 382 | 0.0183 | -1 | c.133 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
AAMDC_chr11_77816144_77877352 | 77869321 | T | C | intron_variant | MODIFIER | NA19240.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0024 | 1 | 382 | 0.0026 | 0 | c.133 others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77869449 | G | A | intron_variant | MODIFIER | HG00741.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0146 | 1 | 382 | 0.0026 | 0 | c.133 others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77869502 | ACGGT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
a0001a0002 | a0001c0002a0002c0003a0002c0004 | a0001c0002t0001a0001c0002t0002a0002c0003t0001others(1): Show | a0001c0002t0001g0009a0001c0002t0001g0012a0001c0002t0001g0019others(153): Show | 160 | 382 | 0.4189 | -4 | c.133 others(19): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
AAMDC_chr11_77816144_77877352 | 77869949 | G | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
a0001a0002 | a0001c0002a0002c0003a0002c0004 | a0001c0002t0001a0001c0002t0002a0002c0003t0001others(1): Show | a0001c0002t0001g0009a0001c0002t0001g0012a0001c0002t0001g0019others(153): Show | 160 | 382 | 0.4189 | 0 | c.228 others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77870185 | T | A | intron_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0170 | 1 | 382 | 0.0026 | 0 | c.228 others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77870199 | A | T | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(129): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0005 | a0001c0001t0001a0001c0002t0001a0003c0005t0001 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0095others(127): Show | 132 | 382 | 0.3456 | 0 | c.228 others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77870329 | A | AT | intron_variant | MODIFIER | HG00423.hp2 HG01074.hp2 HG01167.hp1 others(26): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0002c0003t0001 | a0001c0001t0001g0117a0001c0001t0001g0151a0001c0001t0001g0176others(26): Show | 29 | 382 | 0.0759 | 1 | c.228 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
AAMDC_chr11_77816144_77877352 | 77870329 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(82): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0002c0003t0001others(1): Show | a0001c0001t0001g0096a0001c0001t0001g0118a0001c0001t0001g0128others(80): Show | 85 | 382 | 0.2225 | -1 | c.228 others(8): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
AAMDC_chr11_77816144_77877352 | 77870329 | ATT | A | intron_variant | MODIFIER | HG01109.hp2 HG01168.hp2 HG01884.hp1 others(6): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0002 | a0001c0002t0001g0009a0001c0002t0001g0020a0001c0002t0001g0021others(6): Show | 9 | 382 | 0.0236 | -2 | c.228 others(17): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
AAMDC_chr11_77816144_77877352 | 77870370 | T | A | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
a0001a0002 | a0001c0002a0002c0003a0002c0004 | a0001c0002t0001a0002c0003t0001a0002c0004t0001 | a0001c0002t0001g0076a0001c0002t0001g0078a0001c0002t0001g0079others(67): Show | 72 | 382 | 0.1885 | 0 | c.228 others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77870376 | C | T | intron_variant | MODIFIER | NA18970.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0178 | 1 | 382 | 0.0026 | 0 | c.228 others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77870398 | G | A | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
a0001a0002 | a0001c0002a0002c0003a0002c0004 | a0001c0002t0001a0002c0003t0001a0002c0004t0001 | a0001c0002t0001g0012a0001c0002t0001g0019a0001c0002t0001g0020others(68): Show | 73 | 382 | 0.1911 | 0 | c.228 others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77870589 | A | G | intron_variant | MODIFIER | NA18957.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0317 | 1 | 382 | 0.0026 | 0 | c.228 others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | TogoVar | ||||||
AAMDC_chr11_77816144_77877352 | 77870598 | A | G | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
a0001a0002 | a0001c0002a0002c0003a0002c0004 | a0001c0002t0001a0002c0003t0001a0002c0004t0001 | a0001c0002t0001g0076a0001c0002t0001g0078a0001c0002t0001g0079others(67): Show | 72 | 382 | 0.1885 | 0 | c.228 others(7): Show |
AAMDC | ENSG00000087884.16 | transcript | ENST00000393427.7 | protein_coding | 3/3 | chr11 | TogoVar |