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Table 2 Genetic variants found in eight genes shared by the cases_only (2407 genes) set and the associated_harmful (46 genes) set

From: Exome-wide search and functional annotation of genes associated in patients with severe tick-borne encephalitis in a Russian population

Gene

Harmful genetic variants found in patients with TBE, that are not common in non-Finnish European populations

Harmful genetic variants associated with severe forms of TBE

SNP ID or SNV positiona

Exonic function

SIFT

Polyphen2 HDIV

Polyphen2 HVAR

N b

SNP ID

P-value

Exonic function

SIFT

Polyphen2 HDIV

MAP4 c

rs150907099

nonsyn

D

D

D

1

rs11711953

0.001927

nonsyn

D

D

rs2230169

0.005399

nonsyn

D

D

WDFY4

chr10:50,034,917

nonsyn

D

D

D

1

rs41283283

0.003018

nonsyn

T

D

ACTRT2

rs137950147

nonsyn

T

D

P

1

rs3795263

0.009637

nonsyn

D

D

KLHL25

rs779814173

nonsyn

D

B

B

1

rs35582838

0.009274

nonsyn

D

B

MAP2K3

rs141390631

nonsyn

D

P

D

1

rs74575904

0.002442

nonsyn

D

D

MBD1

rs183864846

nonsyn

D

B

B

1

rs125555

0.009685

nonsyn

D

P

OR10J1

rs35634161

nonsyn

D

D

D

2

rs12048482

0.003306

nonsyn

D

D

rs12409540

0.005492

stopgain

.

.

OR2T34

rs202166093

nonsyn

D

D

D

1

rs199863869

0.001284

nonsyn

D

B

  1. aSNV genomic position was determined according to the GRCh37/hg19 assembly
  2. bN - the occurrence of the rare harmful minor alleles harbored by certain gene in exomes of TBE patients (see Methods section)
  3. cMAP4 has PPI with one gene (IL7R) from the TBEVHostDB