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Table 1 Family characteristics

From: A rare missense variant in APC interrupts splicing and causes AFAP in two Danish families

Individual ID

Gender

Age: Cancer localization (pathology)

Colonic adenomas

Mutation status (APC)

Comments

Family 1

I-I

Female

66: Colon, hepatic flexure (AC)

n/a

n/a

Cholecystitis chronica without specification.

II-I

Female

46: Transverse colon (AC)

> 25

c.289G>A

46: Colectomy

II-II

Male

78: Duodenum (AC)

> 100

c.289G>A

64: Prophylactic subtotal colectomy

II-III

Female

57: Descending colon (AC)

< 10

c.289G>A

57: Subtotal colectomy.

57: Rectum (AC)

57: Transverse colon (AC)

69: Intrahepatic tumor (MCAC)

Caroli disease.

II-VI

Female

55: Breast (IDC)

n/a

n/a

21: Cholecystectomy.

Family 2

I-I

Male

64: Caecum (AC)

n/a

n/a

 

II-I

Female

88: Uterus (EA)

> 30

c.289G>A

*) Suspected based on a CT-scan.

90: Likely pancreatic cancer*

II-II

Male

65: Liver metastases with primary tumor in the gastrointestinal tract, most likely pancreatic or gastric cancer (pathology n/a)

n/a

n/a

 

III-I

Female

62: Sigmoid colon (AC)

Multiple, likely > 100

c.289G>A

62: Total colectomy.

62: Sigmoid colon (AC)

III-II

Male

< 20

c.289G>A

64: No cancer diagnosis.

  1. Abbreviations: AC adenocarcinoma, MCAC mucinous cystadenocarcinoma, IDC invasive ductal carcinoma, EEA endometrioid adenocarcinoma, n/a not available