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Table 2 A list of the most common mutation sites in 31 EOCs

From: Next-generation sequencing-based genomic profiling analysis reveals novel mutations for clinical diagnosis in Chinese primary epithelial ovarian cancer patients

Gene

CHR

POS

Ref

Alt

Count

rsID

FBXW10

chr17

18,682,505

T

C

2

rs1024657

KRTAP4–3

chr17

39,324,333

T

A

2

rs12953139

TP53

chr17

7,577,539

G

A

2

na

ZNF814

chr19

58,385,748

G

A

2

rs145250945

  1. CHR chromosome, POS position of the mutation, Ref reference base, Alt alteration base, Count number of patients sharing a mutation, rsID (reference SNP) - number of known mutations in dbSNP database
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Journal of Ovarian Research

ISSN: 1757-2215

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