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Table 2 Genotypes of all 3 identified variants in 7 available members of the family

From: Whole-exome sequencing reveals a rare missense variant in DTNA in an Iranian pedigree with early-onset atrial fibrillation

Individuals

DTNA(NM_001198943.1) (c.G681C)

NEBL(NM_006393.3) (c.T298C)

SCN5A(NM_001099404.2) (c.A1673G)

III-1

GC

TT

AG

III-3

GG

TT

AG

III-5

GC

TC

AG

IV-2

GC

TT

AG

IV-3

GG

TT

AG

IV-4

GG

TT

AG

IV-5

GC

TC

AG