| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| PLXNA3_chrX_154453281_154482779 | 154467144 | C | CACCA | frameshift_variant others(1): Show |
HIGH | NA18974.hp1 | a0014 | a0014c0018 | a0014c0018t0091 | a0014c0018t0091g0055 | 1 | 262 | 0.0038 | 4 | c.319 others(13): Show |
p.Thr others(6): Show |
PLXNA3 | ENSG00000130827.6 | transcript | ENST00000369682.4 | protein_coding | 18/33 | 3376/10885 | 3201/5616 | 1067/1871 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNA3_chrX_154453281_154482779 | 154472671 | TC | T | frameshift_variant | HIGH | HG00408.hp2 | a0000 | a0000c0020 | a0000c0020t0100 | a0000c0020t0100g0051 | 1 | 262 | 0.0038 | -1 | c.560 others(5): Show |
p.Ser others(6): Show |
PLXNA3 | ENSG00000130827.6 | transcript | ENST00000369682.4 | protein_coding | 33/33 | 5779/10885 | 5604/5616 | 1868/1871 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153765534 | G | GT | frameshift_variant others(1): Show |
HIGH | HG03486.hp1 | a0001 | a0001c0007 | a0001c0007t0012 | a0001c0007t0012g0048 | 1 | 308 | 0.0033 | 1 | c.-1d others(3): Show |
p.Met others(3): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 2/36 | 122/6153 | 1/5730 | 1/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153766908 | C | CA | frameshift_variant | HIGH | NA19086.hp1 | a0031 | a0031c0021 | a0031c0021t0001 | a0031c0021t0001g0084 | 1 | 308 | 0.0033 | 1 | c.81_ others(6): Show |
p.Cys others(4): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 3/36 | 203/6153 | 82/5730 | 28/1909 | chrX | TogoVar | ||
| PLXNB3_chrX_153759249_153784341 | 153767007 | AC | A | frameshift_variant | HIGH | NA19086.hp1 | a0031 | a0031c0021 | a0031c0021t0001 | a0031c0021t0001g0084 | 1 | 308 | 0.0033 | -1 | c.182 others(4): Show |
p.Pro others(4): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 3/36 | 303/6153 | 182/5730 | 61/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153767297 | AC | A | frameshift_variant | HIGH | NA19086.hp1 | a0031 | a0031c0021 | a0031c0021t0001 | a0031c0021t0001g0084 | 1 | 308 | 0.0033 | -1 | c.473 others(4): Show |
p.Pro others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 3/36 | 594/6153 | 473/5730 | 158/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153767348 | T | TG | frameshift_variant | HIGH | NA19086.hp1 | a0031 | a0031c0021 | a0031c0021t0001 | a0031c0021t0001g0084 | 1 | 308 | 0.0033 | 1 | c.525 others(4): Show |
p.Leu others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 3/36 | 647/6153 | 526/5730 | 176/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153767463 | GC | G | frameshift_variant | HIGH | NA19089.hp1 | a0030 | a0030c0058 | a0030c0058t0001 | a0030c0058t0001g0052 | 1 | 308 | 0.0033 | -1 | c.639 others(4): Show |
p.Phe others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 3/36 | 760/6153 | 639/5730 | 213/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153767584 | GC | G | frameshift_variant | HIGH | NA19089.hp1 | a0030 | a0030c0058 | a0030c0058t0001 | a0030c0058t0001g0052 | 1 | 308 | 0.0033 | -1 | c.760 others(4): Show |
p.Arg others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 3/36 | 881/6153 | 760/5730 | 254/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153767731 | G | GT | frameshift_variant | HIGH | NA19089.hp1 | a0030 | a0030c0058 | a0030c0058t0001 | a0030c0058t0001g0052 | 1 | 308 | 0.0033 | 1 | c.905 others(4): Show |
p.Phe others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 3/36 | 1027/6153 | 906/5730 | 302/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153767902 | A | AC | frameshift_variant | HIGH | NA18956.hp1 | a0028 | a0028c0029 | a0028c0029t0001 | a0028c0029t0001g0070 | 1 | 308 | 0.0033 | 1 | c.107 others(5): Show |
p.Leu others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 3/36 | 1200/6153 | 1079/5730 | 360/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153768285 | A | AC | frameshift_variant | HIGH | NA19086.hp1 | a0031 | a0031c0021 | a0031c0021t0001 | a0031c0021t0001g0084 | 1 | 308 | 0.0033 | 1 | c.112 others(5): Show |
p.Ser others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 4/36 | 1250/6153 | 1129/5730 | 377/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153768361 | TG | T | frameshift_variant | HIGH | NA19086.hp1 | a0031 | a0031c0021 | a0031c0021t0001 | a0031c0021t0001g0084 | 1 | 308 | 0.0033 | -1 | c.120 others(5): Show |
p.Ala others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 4/36 | 1322/6153 | 1201/5730 | 401/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153769917 | A | AC | frameshift_variant | HIGH | NA18941.hp2 | a0013 | a0013c0032 | a0013c0032t0004 | a0013c0032t0004g0085 | 1 | 308 | 0.0033 | 1 | c.161 others(5): Show |
p.Arg others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 7/36 | 1734/6153 | 1613/5730 | 538/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153770569 | GC | G | frameshift_variant | HIGH | NA19086.hp1 | a0031 | a0031c0021 | a0031c0021t0001 | a0031c0021t0001g0084 | 1 | 308 | 0.0033 | -1 | c.194 others(5): Show |
p.Pro others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 10/36 | 2061/6153 | 1940/5730 | 647/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153770976 | C | CT | frameshift_variant | HIGH | NA18941.hp2 | a0013 | a0013c0032 | a0013c0032t0004 | a0013c0032t0004g0085 | 1 | 308 | 0.0033 | 1 | c.214 others(5): Show |
p.Ser others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 12/36 | 2271/6153 | 2150/5730 | 717/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153771056 | G | GC | frameshift_variant | HIGH | NA18941.hp2 | a0013 | a0013c0032 | a0013c0032t0004 | a0013c0032t0004g0085 | 1 | 308 | 0.0033 | 1 | c.223 others(5): Show |
p.Leu others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 12/36 | 2352/6153 | 2231/5730 | 744/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153771362 | A | AG | frameshift_variant | HIGH | NA18941.hp2 | a0013 | a0013c0032 | a0013c0032t0004 | a0013c0032t0004g0085 | 1 | 308 | 0.0033 | 1 | c.230 others(5): Show |
p.Glu others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 13/36 | 2431/6153 | 2310/5730 | 770/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153771511 | C | CCA | frameshift_variant | HIGH | NA18941.hp2 | a0013 | a0013c0032 | a0013c0032t0004 | a0013c0032t0004g0085 | 1 | 308 | 0.0033 | 2 | c.237 others(11): Show |
p.Pro others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 14/36 | 2498/6153 | 2377/5730 | 793/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153771525 | GC | G | frameshift_variant | HIGH | NA19086.hp1 | a0031 | a0031c0021 | a0031c0021t0001 | a0031c0021t0001g0084 | 1 | 308 | 0.0033 | -1 | c.238 others(5): Show |
p.His others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 14/36 | 2510/6153 | 2389/5730 | 797/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153771598 | G | GC | frameshift_variant | HIGH | NA18941.hp2 | a0013 | a0013c0032 | a0013c0032t0004 | a0013c0032t0004g0085 | 1 | 308 | 0.0033 | 1 | c.246 others(5): Show |
p.Cys others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 14/36 | 2585/6153 | 2464/5730 | 822/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153771634 | T | TC | frameshift_variant | HIGH | NA18941.hp2 | a0013 | a0013c0032 | a0013c0032t0004 | a0013c0032t0004g0085 | 1 | 308 | 0.0033 | 1 | c.249 others(5): Show |
p.Ala others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 14/36 | 2620/6153 | 2499/5730 | 833/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153771878 | C | CG | frameshift_variant | HIGH | NA18977.hp1 | a0026 | a0026c0040 | a0026c0040t0001 | a0026c0040t0001g0002 | 1 | 308 | 0.0033 | 1 | c.253 others(5): Show |
p.Pro others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 15/36 | 2656/6153 | 2535/5730 | 845/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153771880 | G | GT | frameshift_variant | HIGH | NA18941.hp2 | a0013 | a0013c0032 | a0013c0032t0004 | a0013c0032t0004g0085 | 1 | 308 | 0.0033 | 1 | c.253 others(5): Show |
p.Pro others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 15/36 | 2657/6153 | 2536/5730 | 846/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153771946 | T | TG | frameshift_variant | HIGH | NA19086.hp1 | a0031 | a0031c0021 | a0031c0021t0001 | a0031c0021t0001g0084 | 1 | 308 | 0.0033 | 1 | c.260 others(5): Show |
p.Gln others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 15/36 | 2723/6153 | 2602/5730 | 868/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153771980 | C | CA | frameshift_variant | HIGH | NA18941.hp2 | a0013 | a0013c0032 | a0013c0032t0004 | a0013c0032t0004g0085 | 1 | 308 | 0.0033 | 1 | c.263 others(5): Show |
p.Asn others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 15/36 | 2758/6153 | 2637/5730 | 879/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153771989 | G | GC | frameshift_variant | HIGH | NA18941.hp2 | a0013 | a0013c0032 | a0013c0032t0004 | a0013c0032t0004g0085 | 1 | 308 | 0.0033 | 1 | c.264 others(5): Show |
p.Ser others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 15/36 | 2768/6153 | 2647/5730 | 883/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153772231 | C | CG | frameshift_variant | HIGH | NA18941.hp2 | a0013 | a0013c0032 | a0013c0032t0004 | a0013c0032t0004g0085 | 1 | 308 | 0.0033 | 1 | c.272 others(5): Show |
p.Val others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 16/36 | 2844/6153 | 2723/5730 | 908/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153772255 | C | CCA | frameshift_variant | HIGH | NA18941.hp2 | a0013 | a0013c0032 | a0013c0032t0004 | a0013c0032t0004g0085 | 1 | 308 | 0.0033 | 2 | c.274 others(11): Show |
p.Gly others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 16/36 | 2867/6153 | 2746/5730 | 916/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153772278 | C | CA | frameshift_variant | HIGH | NA19086.hp1 | a0031 | a0031c0021 | a0031c0021t0001 | a0031c0021t0001g0084 | 1 | 308 | 0.0033 | 1 | c.276 others(5): Show |
p.Thr others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 16/36 | 2889/6153 | 2768/5730 | 923/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153772902 | G | GA | frameshift_variant | HIGH | NA18941.hp2 | a0013 | a0013c0032 | a0013c0032t0004 | a0013c0032t0004g0085 | 1 | 308 | 0.0033 | 1 | c.279 others(10): Show |
p.Ser others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 17/36 | 2914/6153 | 2793/5730 | 931/1909 | chrX | TogoVar | ||
| PLXNB3_chrX_153759249_153784341 | 153772920 | G | GC | frameshift_variant | HIGH | NA18941.hp2 | a0013 | a0013c0032 | a0013c0032t0004 | a0013c0032t0004g0085 | 1 | 308 | 0.0033 | 1 | c.281 others(5): Show |
p.Gln others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 17/36 | 2937/6153 | 2816/5730 | 939/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153773241 | T | TG | frameshift_variant | HIGH | NA19086.hp1 | a0031 | a0031c0021 | a0031c0021t0001 | a0031c0021t0001g0084 | 1 | 308 | 0.0033 | 1 | c.291 others(5): Show |
p.Cys others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 18/36 | 3041/6153 | 2920/5730 | 974/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153773301 | T | TC | frameshift_variant | HIGH | NA18941.hp2 | a0013 | a0013c0032 | a0013c0032t0004 | a0013c0032t0004g0085 | 1 | 308 | 0.0033 | 1 | c.298 others(5): Show |
p.Leu others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 18/36 | 3102/6153 | 2981/5730 | 994/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153773311 | C | CT | frameshift_variant | HIGH | NA18941.hp2 | a0013 | a0013c0032 | a0013c0032t0004 | a0013c0032t0004g0085 | 1 | 308 | 0.0033 | 1 | c.299 others(5): Show |
p.Gly others(5): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 18/36 | 3113/6153 | 2992/5730 | 998/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153773324 | C | CT | frameshift_variant | HIGH | NA19086.hp1 | a0031 | a0031c0021 | a0031c0021t0001 | a0031c0021t0001g0084 | 1 | 308 | 0.0033 | 1 | c.300 others(10): Show |
p.Gln others(6): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 18/36 | 3123/6153 | 3002/5730 | 1001/1909 | chrX | TogoVar | ||
| PLXNB3_chrX_153759249_153784341 | 153773519 | G | GA | frameshift_variant others(1): Show |
HIGH | NA18941.hp2 | a0013 | a0013c0032 | a0013c0032t0004 | a0013c0032t0004g0085 | 1 | 308 | 0.0033 | 1 | c.308 others(10): Show |
p.Gly others(6): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 19/36 | 3207/6153 | 3086/5730 | 1029/1909 | chrX | TogoVar | ||
| PLXNB3_chrX_153759249_153784341 | 153773544 | G | GC | frameshift_variant | HIGH | NA18941.hp2 | a0013 | a0013c0032 | a0013c0032t0004 | a0013c0032t0004g0085 | 1 | 308 | 0.0033 | 1 | c.311 others(5): Show |
p.Thr others(6): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 19/36 | 3233/6153 | 3112/5730 | 1038/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153773594 | G | GA | frameshift_variant | HIGH | NA18941.hp2 | a0013 | a0013c0032 | a0013c0032t0004 | a0013c0032t0004g0085 | 1 | 308 | 0.0033 | 1 | c.316 others(10): Show |
p.Ala others(6): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 19/36 | 3282/6153 | 3161/5730 | 1054/1909 | chrX | TogoVar | ||
| PLXNB3_chrX_153759249_153784341 | 153773698 | TG | T | frameshift_variant | HIGH | NA19086.hp1 | a0031 | a0031c0021 | a0031c0021t0001 | a0031c0021t0001g0084 | 1 | 308 | 0.0033 | -1 | c.327 others(5): Show |
p.Leu others(6): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 19/36 | 3391/6153 | 3270/5730 | 1090/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153774053 | T | TA | frameshift_variant | HIGH | NA19086.hp1 | a0031 | a0031c0021 | a0031c0021t0001 | a0031c0021t0001g0084 | 1 | 308 | 0.0033 | 1 | c.347 others(10): Show |
p.Ala others(6): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 20/36 | 3596/6153 | 3475/5730 | 1159/1909 | chrX | TogoVar | ||
| PLXNB3_chrX_153759249_153784341 | 153774267 | A | AC | frameshift_variant | HIGH | NA19082.hp1 | a0022 | a0022c0043 | a0022c0043t0001 | a0022c0043t0001g0001 | 1 | 308 | 0.0033 | 1 | c.360 others(5): Show |
p.Arg others(6): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 21/36 | 3724/6153 | 3603/5730 | 1201/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153774273 | A | AC | frameshift_variant | HIGH | NA18977.hp1 | a0026 | a0026c0040 | a0026c0040t0001 | a0026c0040t0001g0002 | 1 | 308 | 0.0033 | 1 | c.361 others(5): Show |
p.His others(6): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 21/36 | 3732/6153 | 3611/5730 | 1204/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153774448 | T | TG | frameshift_variant | HIGH | NA19058.hp1 | a0015 | a0015c0037 | a0015c0037t0008 | a0015c0037t0008g0112 | 1 | 308 | 0.0033 | 1 | c.371 others(5): Show |
p.Val others(6): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 22/36 | 3832/6153 | 3711/5730 | 1237/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153774473 | A | AC | frameshift_variant | HIGH | NA18994.hp1 | a0016 | a0016c0034 | a0016c0034t0001 | a0016c0034t0001g0027 | 1 | 308 | 0.0033 | 1 | c.373 others(5): Show |
p.Leu others(6): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 22/36 | 3859/6153 | 3738/5730 | 1246/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153774558 | AC | A | frameshift_variant | HIGH | NA19086.hp1 | a0031 | a0031c0021 | a0031c0021t0001 | a0031c0021t0001g0084 | 1 | 308 | 0.0033 | -1 | c.382 others(5): Show |
p.Leu others(6): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 22/36 | 3941/6153 | 3820/5730 | 1274/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153776000 | C | CT | frameshift_variant | HIGH | NA19003.hp2 | a0025 | a0025c0041 | a0025c0041t0010 | a0025c0041t0010g0056 | 1 | 308 | 0.0033 | 1 | c.451 others(5): Show |
p.Leu others(6): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 27/36 | 4639/6153 | 4518/5730 | 1506/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153776007 | CG | C | frameshift_variant | HIGH | NA19058.hp1 | a0015 | a0015c0037 | a0015c0037t0008 | a0015c0037t0008g0112 | 1 | 308 | 0.0033 | -1 | c.452 others(5): Show |
p.Glu others(6): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 27/36 | 4646/6153 | 4525/5730 | 1509/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153776066 | C | CG | frameshift_variant | HIGH | HG01516.hp1 HG03491.hp1 NA18967.hp1 others(1): Show |
a0006a0018 | a0006c0019a0006c0046a0018c0036 | a0006c0019t0001a0006c0046t0001a0018c0036t0001 | a0006c0019t0001g0001a0006c0046t0001g0002a0018c0036t0001g0118 | 4 | 308 | 0.0130 | 1 | c.458 others(5): Show |
p.Ala others(6): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 27/36 | 4707/6153 | 4586/5730 | 1529/1909 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |
| PLXNB3_chrX_153759249_153784341 | 153776108 | G | GT | frameshift_variant | HIGH | NA19003.hp2 | a0025 | a0025c0041 | a0025c0041t0010 | a0025c0041t0010g0056 | 1 | 308 | 0.0033 | 1 | c.462 others(10): Show |
p.Val others(6): Show |
PLXNB3 | ENSG00000198753.12 | transcript | ENST00000361971.10 | protein_coding | 27/36 | 4745/6153 | 4624/5730 | 1542/1909 | chrX | TogoVar |