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Table 3 The 15 filtered Variant IDs (nsSNPs) with bioinformatics SNP tools scores

From: Non-synonymous SNPs variants of PRKCG and its association with oncogenes predispose to hepatocellular carcinoma

Variant ID

Chr: bp

vf_allele

Alleles

AA

AA coord

rs797045900

19:53882648

A

T/A

C/S

52

rs386134162

19:53889693

A

G/A

C/Y

114

rs1064797249

19:53889695

T

G/T

D/Y

115

rs1568752939

19:53889734

C

G/C

G/R

128

rs386134167

19:53889744

A

G/A

C/Y

131

rs1192424800

19:53889900

A

G/A

V/M

138

rs1599943341

19:53889936

C

T/C

C/R

150

rs866406014

19:53889963

A

G/A

G/R

159

rs386134171

19:53898097

A

G/A

G/S

360

rs747522330

19:53898555

C

T/C

L/P

403

rs1398783758

19:53900448

C

T/C

L/P

468

rs387906679

19:53900612

T

G/T

D/Y

480

rs1202130595

19:53900736

G

A/G

Y/C

521

rs1568764306

19:53906342

A

G/A

R/H

597

rs121918516

19:53906728

C

T/C

F/L

643