Somatic mutation in CTCL patient samples
Case . | Position (hg19) . | Ref/Alt . | Ensemble_Gene . | Ensemble_Transcript . | Ensemble_Protein . | Consequence . | Pos. CDS . | Pos. protein . | aa change . | SIFT prediction . | Gene name . |
---|---|---|---|---|---|---|---|---|---|---|---|
01 | 2:242793386 | G/A | ENSG00000188389 | ENST00000334409 | ENSP00000335062 | STOP_GAINED | 691 | 231 | R/* | truncated | PDCD1 |
02 | 17:7579390/1 | CC/TT | ENSG00000141510 | ENST00000269305 | ENSP00000269305 | MISSENSE | 296 | 99 | S/F | deleterious | TP53 |
02 | 20:39792584 | C/T | ENSG00000124181 | ENST00000373271 | ENSP00000362368 | MISSENSE | 1034 | 345 | S/F | deleterious | PLCG1 |
02 | 5:55256271 | C/G | ENSG00000134352 | ENST00000381294 | ENSP00000370694 | MISSENSE | 932 | 311 | S/T | deleterious | IL6ST |
03 | 3:32995957 | C/A | ENSG00000183813 | ENST00000330953 | ENSP00000332659 | MISSENSE | 1043 | 348 | T/K | deleterious | CCR4 |
04 | 2:46985980 | C/G | ENSG00000171150 | ENST00000306503 | ENSP00000305133 | MISSENSE | 311 | 104 | P/R | deleterious | SOCS5 |
05 | 13:48951093- 48951115 | GTGAAGGATATAGGATACATCTT/TATCC- | ENSG00000139687 | ENST00000267163 | ENSP00000267163 | FRAMESHIFT | 1255-1277 | 419 | — | truncated | RB1 |
05 | 1:65312344 | G/A | ENSG00000162434 | ENST00000342505 | ENSP00000343204 | MISSENSE | 1975 | 659 | R/C | tolerated | JAK1 |
06 | 20:39792584/5 | CC/TT | ENSG00000124181 | ENST00000373271 | ENSP00000362368 | MISSENSE | 1034 | 345 | S/F | deleterious | PLCG1 |
06 | 1:173930910 | A/T | ENSG00000135870 | ENST00000367696 | ENSP00000356669 | MISSENSE | 2155 | 719 | Y/N | deleterious | RC3H1 |
06 | 16:31332895 | A/T | ENSG00000169896 | ENST00000544665 | ENSP00000441691 | MISSENSE | 1952 | 651 | E/V | tolerated | ITGAM |
06 | 19:55512230 | G/A | ENSG00000022556 | ENST00000543010 | ENSP00000445135 | STOP_GAINED | 3153 | 1051 | W/* | truncated | NLRP2 |
07 | 11:36511782 | C/T | ENSG00000175104 | ENST00000526995 | ENSP00000433623 | MISSENSE | 1175 | 392 | R/H | deleterious | TRAF6 |
08 | 8:19805850 | C/T | ENSG00000175445 | ENST00000311322 | ENSP00000309757 | MISSENSE | 248 | 83 | T/M | deleterious | LPL |
08 | 20:39794139 | C/T | ENSG00000124181 | ENST00000373271 | ENSP00000362368 | MISSENSE | 1559 | 520 | S/F | deleterious | PLCG1 |
08 | 19:42383212/3 | CC/TT | ENSG00000105369 | ENST00000221972 | ENSP00000221972 | MISSENSE | 232-233 | 78 | P/F | deleterious | CD79A |
08 | 11:47376813 | C/T | ENSG00000066336 | ENST00000378538 | ENSP00000367799 | MISSENSE | 778 | 260 | G/R | tolerated | SPI1 |
08 | 7:42005556 | C/T | ENSG00000106571 | ENST00000395925 | ENSP00000379258 | MISSENSE | 3115 | 1039 | A/T | tolerated | GLI3 |
08 | 19:45537775 | A/C | ENSG00000104856 | ENST00000221452 | ENSP00000221452 | MISSENSE | 1343 | 448 | N/T | tolerated | RELB |
08 | 17:7574003 | G/A | ENSG00000141510 | ENST00000269305 | ENSP00000269305 | STOP_GAINED | 1024 | 342 | R/* | truncated | TP53 |
09 | X:39921444 | T/C | ENSG00000183337 | ENST00000397354 | ENSP00000380512 | MISSENSE | 4274 | 1425 | N/S | deleterious | BCOR |
09 | 6:137112905 | G/C | ENSG00000197442 | ENST00000359015 | ENSP00000351908 | MISSENSE | 391 | 131 | H/D | tolerated | MAP3K5 |
10 | 2: 242076565 | G/A | ENSG00000115687 | ENST00000405260 | ENSP00000384016 | MISSENSE | 991 | 331 | P/S | tolerated | PASK |
10 | 7: 2976811 | C/T | ENSG00000198286 | ENST00000396946 | ENSP00000380150 | MISSENSE | 1201 | 401 | D/N | deleterious | CARD11 |
10 | 20:9561459 | G/A | ENSG00000101349 | ENST00000378429 | ENSP00000367686 | MISSENSE | 323 | 108 | P/L | tolerated | PAK7 |
10 | 19:17949108 | C/T | ENSG00000105639 | ENST00000458235 | ENSP00000391676 | MISSENSE | 1533 | 511 | M/I | tolerated | JAK3 |
11 | NO MUT |
Case . | Position (hg19) . | Ref/Alt . | Ensemble_Gene . | Ensemble_Transcript . | Ensemble_Protein . | Consequence . | Pos. CDS . | Pos. protein . | aa change . | SIFT prediction . | Gene name . |
---|---|---|---|---|---|---|---|---|---|---|---|
01 | 2:242793386 | G/A | ENSG00000188389 | ENST00000334409 | ENSP00000335062 | STOP_GAINED | 691 | 231 | R/* | truncated | PDCD1 |
02 | 17:7579390/1 | CC/TT | ENSG00000141510 | ENST00000269305 | ENSP00000269305 | MISSENSE | 296 | 99 | S/F | deleterious | TP53 |
02 | 20:39792584 | C/T | ENSG00000124181 | ENST00000373271 | ENSP00000362368 | MISSENSE | 1034 | 345 | S/F | deleterious | PLCG1 |
02 | 5:55256271 | C/G | ENSG00000134352 | ENST00000381294 | ENSP00000370694 | MISSENSE | 932 | 311 | S/T | deleterious | IL6ST |
03 | 3:32995957 | C/A | ENSG00000183813 | ENST00000330953 | ENSP00000332659 | MISSENSE | 1043 | 348 | T/K | deleterious | CCR4 |
04 | 2:46985980 | C/G | ENSG00000171150 | ENST00000306503 | ENSP00000305133 | MISSENSE | 311 | 104 | P/R | deleterious | SOCS5 |
05 | 13:48951093- 48951115 | GTGAAGGATATAGGATACATCTT/TATCC- | ENSG00000139687 | ENST00000267163 | ENSP00000267163 | FRAMESHIFT | 1255-1277 | 419 | — | truncated | RB1 |
05 | 1:65312344 | G/A | ENSG00000162434 | ENST00000342505 | ENSP00000343204 | MISSENSE | 1975 | 659 | R/C | tolerated | JAK1 |
06 | 20:39792584/5 | CC/TT | ENSG00000124181 | ENST00000373271 | ENSP00000362368 | MISSENSE | 1034 | 345 | S/F | deleterious | PLCG1 |
06 | 1:173930910 | A/T | ENSG00000135870 | ENST00000367696 | ENSP00000356669 | MISSENSE | 2155 | 719 | Y/N | deleterious | RC3H1 |
06 | 16:31332895 | A/T | ENSG00000169896 | ENST00000544665 | ENSP00000441691 | MISSENSE | 1952 | 651 | E/V | tolerated | ITGAM |
06 | 19:55512230 | G/A | ENSG00000022556 | ENST00000543010 | ENSP00000445135 | STOP_GAINED | 3153 | 1051 | W/* | truncated | NLRP2 |
07 | 11:36511782 | C/T | ENSG00000175104 | ENST00000526995 | ENSP00000433623 | MISSENSE | 1175 | 392 | R/H | deleterious | TRAF6 |
08 | 8:19805850 | C/T | ENSG00000175445 | ENST00000311322 | ENSP00000309757 | MISSENSE | 248 | 83 | T/M | deleterious | LPL |
08 | 20:39794139 | C/T | ENSG00000124181 | ENST00000373271 | ENSP00000362368 | MISSENSE | 1559 | 520 | S/F | deleterious | PLCG1 |
08 | 19:42383212/3 | CC/TT | ENSG00000105369 | ENST00000221972 | ENSP00000221972 | MISSENSE | 232-233 | 78 | P/F | deleterious | CD79A |
08 | 11:47376813 | C/T | ENSG00000066336 | ENST00000378538 | ENSP00000367799 | MISSENSE | 778 | 260 | G/R | tolerated | SPI1 |
08 | 7:42005556 | C/T | ENSG00000106571 | ENST00000395925 | ENSP00000379258 | MISSENSE | 3115 | 1039 | A/T | tolerated | GLI3 |
08 | 19:45537775 | A/C | ENSG00000104856 | ENST00000221452 | ENSP00000221452 | MISSENSE | 1343 | 448 | N/T | tolerated | RELB |
08 | 17:7574003 | G/A | ENSG00000141510 | ENST00000269305 | ENSP00000269305 | STOP_GAINED | 1024 | 342 | R/* | truncated | TP53 |
09 | X:39921444 | T/C | ENSG00000183337 | ENST00000397354 | ENSP00000380512 | MISSENSE | 4274 | 1425 | N/S | deleterious | BCOR |
09 | 6:137112905 | G/C | ENSG00000197442 | ENST00000359015 | ENSP00000351908 | MISSENSE | 391 | 131 | H/D | tolerated | MAP3K5 |
10 | 2: 242076565 | G/A | ENSG00000115687 | ENST00000405260 | ENSP00000384016 | MISSENSE | 991 | 331 | P/S | tolerated | PASK |
10 | 7: 2976811 | C/T | ENSG00000198286 | ENST00000396946 | ENSP00000380150 | MISSENSE | 1201 | 401 | D/N | deleterious | CARD11 |
10 | 20:9561459 | G/A | ENSG00000101349 | ENST00000378429 | ENSP00000367686 | MISSENSE | 323 | 108 | P/L | tolerated | PAK7 |
10 | 19:17949108 | C/T | ENSG00000105639 | ENST00000458235 | ENSP00000391676 | MISSENSE | 1533 | 511 | M/I | tolerated | JAK3 |
11 | NO MUT |
aa, aminoacid; Alt, altered base; CDS, coding sequence; Pos, position; Ref, reference base; SIFT, “sorting tolerant from intolerant” algorithm.