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. 2023 Aug 25;26(10):107735. doi: 10.1016/j.isci.2023.107735

Table 5.

T cell receptor beta variable (TRBV) genes with significantly different allele frequency variants between cases and controls

TCR GENES
TRBV5_5
TRBV6_5
TRBV7_3
TRBV7_6
TRBV7_7
TRBV7_8
TRBV10_1
TRBV30
#Variants of Concern in Gene
1
3
4
3
3
3
7
1
PATIENT ID #HI Alleles #HI Alleles #HI Alleles #HI Alleles #HI Alleles #HI Alleles #HI Alleles #HI Alleles
AR5440 1 3 4 3 3 2 7 2
AR5443 1 3 4 3 3 3 8 0
AR5444 1 3 4 3 3 3 6 0
AR5445 1 3 4 3 3 0 6 1
AR5446 1 3 4 3 3 3 8 1
AR5447 1 3 4 3 3 3 7 0
AR5448 1 3 4 3 3 2 7 0
AR5449 1 3 4 3 3 2 6 1
AR5450 1 3 4 3 3 3 7 2
AR5451 1 3 4 3 3 0 7 0
AR5452 1 3 4 3 3 0 6 2
AR5454 1 3 4 3 3 3 7 0
AR5455 1 3 4 3 3 0 7 0
AR5457 1 3 4 3 3 2 7 0
AR5458 1 3 4 3 3 3 6 2
AR5459 1 3 4 3 3 3 8 0
AR5460 1 3 4 3 3 2 7 0
AR5461 1 3 4 3 3 0 7 0
AR5462 1 3 4 3 3 3 6 1
AR5463 1 3 4 3 3 3 7 0
AR5464 1 3 4 3 3 0 6 1
AR5465 1 3 2 3 3 0 7 2
AR5466 1 3 4 3 3 3 7 1
AR5467 1 3 4 3 3 2 7 0
AR5468 1 3 4 3 3 2 7 2
AR5469 1 3 4 3 3 3 8 0
AR5470 1 3 4 3 3 3 7 1
AR5472 1 3 4 3 3 3 6 0
AR5473 1 3 4 3 3 3 7 1
AR5474 1 3 4 3 3 0 8 0
AR5475 1 3 4 3 3 0 7 1
AR5476 1 3 4 3 3 0 8 0
AR5477 1 3 4 3 3 3 8 0
AR5478 1 3 4 3 3 0 7 1
AR5481 1 3 4 3 3 0 8 1
AR5484 1 3 4 3 3 0 7 0
AR5485 1 3 4 3 3 0 6 0
AR5486 1 3 4 3 3 3 6 0
AR5487 1 3 4 3 3 0 7 1
AR5488 1 3 4 3 3 3 7 2
AR5490 1 3 4 3 3 0 6 0
AR5492 1 3 4 3 3 3 7 0
AR5493 1 3 4 3 3 3 7 2
AR5495 1 3 4 3 3 2 6 1
AR5496 1 3 4 3 3 3 7 1
AR5497 1 3 4 3 3 3 6 0
AR5499 1 3 4 3 3 2 7 0
AR5500 1 3 4 3 3 2 8 1
AR5501 1 3 4 3 3 0 6 0
AR5502 1 3 4 3 3 3 7 2
AR5503 1 3 4 3 3 0 7 0
AR5506 1 3 4 3 3 3 7 1
AR5507 1 3 4 3 3 0 7 1
AR5508 1 3 4 3 3 3 6 1
AR5510 1 3 4 3 3 3 7 1
AR5511 1 3 4 3 3 3 8 0
AR5512 1 3 4 3 3 0 8 0
AR5513 1 3 4 3 3 0 8 1
AR5514 1 3 4 3 3 3 8 1
AR5516 1 3 4 3 3 2 7 0
AR5517 1 3 4 3 3 3 6 2
AR5518 1 3 4 3 3 2 7 1
AR5520 1 3 4 3 3 3 7 1
AR5521 1 3 4 3 3 3 6 1
AR5522 1 3 4 3 3 2 7 1
AR5524 1 3 4 3 3 3 7 2
AR5526 1 3 4 3 3 2 7 1
AR5527 1 3 4 3 3 2 8 0
AR5530 1 3 4 3 3 2 7 1
AR5533 1 3 4 3 3 2 6 0
AR5535 1 3 4 3 3 3 8 1
AR5536 1 3 4 3 3 0 8 2
AR5538 1 3 4 3 3 3 7 0
AR5539 1 3 4 3 3 3 6 0

For each gene we highlight the total number of variants of concern as well as the number of high impact alleles each patient has in each gene for those variants. In red we highlight those genes containing more than 3 high impact alleles, indicating a potential loss of function in both alleles for the gene.