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Table 5 Family-specific common and rare variants in Family C

From: Identification of novel candidate variants including COL6A6 polymorphisms in early-onset atopic dermatitis using whole-exome sequencing

 

Common variant

Functional prediction program

Gene

#RS

Chr

POS

Amino acid change

Type

SIFT

Polyphen2

PhyloP

PhastCons

Global

East Asian

Korean

UVSSA

2276904

chr4

1,349,029

R391H

cSNP

.

.

.

.

0.23

0.42

0.374

HGFAC

3748034

chr4

3,446,091

A218S

cSNP

0.38

0.659

2

1

0.15

0.28

0.305

UNC93A

2235197

chr6

167,709,702

W151

STOP GAINED

.

.

4.525

1

0.1

0.15

0.163

ABCA13

17712299

chr7

48,313,881

F1540L

cSNP

.

0.997

2.325

0.85

0.11

0.17

0.255

SSPO

1005603

chr7

149,516,881

S4028I

cSNP

.

.

.

1

0.2

0.19

0.181

TTC40

.

chr10

134,679,632

T1596M

cSNP

.

.

.

.

.

 

.

Rare variant

 

COL6A6

200963433

chr3

130,289,976

R906C

cSNP

0

1

4.596

1

0.0014

0.01

0.017

CDX1

370852694

chr5

149,546,819

A127E

cSNP

0.87

0.458

1.235

0.996

.

.

0.027