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Table 1 SNPs of high and moderate predicted impact in CAMA-1_ribociclib_resistant cells compared to parental CAMA-1 cells

From: Exploiting collateral sensitivity controls growth of mixed culture of sensitive and resistant cells and decreases selection for resistant cells in a cell line model

Gene symbol

Predicted SNP impact

Predicted SNP effect

Detected mutation

Gene’s implication in cancer prognosis/progression

MIA3

High

Stop gained

c.2335A>T

p.Lys779*

 

BTLA

High

Stop gained

c.94G>T

p.Glu32*

 

SAMD9

High

Stop gained

c.2827G>T

p.Gly943*

 

ARMCX2

High

Stop gained

c.1055C>A

p.Ser352*

 

WDFY3

High

Stop gained

c.7504C>T

p.Gln2502*

 

SEMA6A

High

Stop gained

c.270T>A

p.Tyr90*

Benign prognostic factor in glioblastoma [53]

ALDH5A1

High

Structural interaction variant

c.844T>C

p.Phe282Leu

Benign prognostic factor in high-grade serous ovarian carcinoma [54]

ARHGDIA

High

Structural interaction variant

c.573C>A

p.Ser191Ser

Benign prognostic factor in glioma [55]

MAPKBP1

High

Stop gained

c.3268G>T

p.Glu1090*

 

SORCS1

Moderate

Missense variant

c.2303G>A

p.Gly768Glu

 

RAG1

Moderate

Missense variant

c.2023C>A

p.Leu675Met

 

NEUROD4

Moderate

Missense variant

c.204G>T

p.Lys68Asn

 

NALCN

Moderate

Missense variant

c.2091T>G

p.Ile697Met

Somatic mutations in pancreatic ductal adenocarcinomas [64]

AHNAK2

Moderate

Missense variant

c.12994G>A

p.Val4332Met

Correlates with poor prognosis in pancreatic ductal adenocarcinomas [65]

MYO9A

Moderate

Missense variant

c.4708G>C

p.Glu1570Gln

 

CHD2

Moderate

Missense variant

c.595C>T

p.Arg199Cys

 

CNTNAP1

Moderate

Missense variant

c.2109C>G

p.Phe703Leu

 

NLRP5

Moderate

Missense variant

c.2448G>A

p.Met816Ile

 

HEATR5B

Moderate

Missense variant

c.307G>T

p.Asp103Tyr

 

SPTBN1

Moderate

Missense variant

c.5222G>T

p.Arg1741Leu

 

TTC3

Moderate

Missense variant

c.3788G>C

p.Arg1263Thr

 

ZNF502

Moderate

Missense variant

c.503C>T

p.Ser168Leu

 

CRYBG3

Moderate

Missense variant

c.1753A>G

p.Lys585Glu

 

BMP3

Moderate

Missense variant

c.845C>A

p.Ser282Tyr

 

TREML2

Moderate

Missense variant

c.496A>C

p.Met166Leu

 

DPYD

Moderate

Missense variant

c.384G>T

p.Met128Ile

 

RASAL2

Moderate

Missense variant

c.199C>T

p.Arg67Trp

 

CFAP46

Moderate

Missense variant

c.1333G>T

p.Ala445Ser

 

CEP83

Moderate

Missense variant

c.380A>G

p.Glu127Gly

 

TSPOAP1

Moderate

Missense variant

c.3004C>A

p.Pro1002Thr

 

ZNF761

Moderate

Missense variant

c.1492G>C

p.Glu498Gln

 

PAXIP1

Moderate

Missense variant

c.2004A>T

p.Arg668Ser

 

RP1

Moderate

Missense variant

c.5123C>A

p.Ala1708Asp

Somatic mutations in intramedullary spinal cord ependimomas [66]

NCOA2

Moderate

Missense variant

c.3320G>T

p.Ser1107Ile

Frequently amplified in breast cancer [67]

GLYR1

Moderate

Missense variant

c.1336G>C

p.Ala446Pro

 

DNAAF4

Moderate

Missense variant

c.572A>G

p.Glu191Gly

 

CYP3A43

Moderate

Missense variant

c.1154T>C

p.Leu385Ser

 

LRP4

Moderate

Missense variant

c.4798C>T

p.Leu1600Phe

 

F11

Moderate

Missense variant

c.1654C>A

p.His552Asn

 

CCDC166

Moderate

Missense variant

c.67G>C

p.Ala23Pro

 

ANKRD22

Moderate

Missense variant

c.1253G>A

p.Arg418Gln

Correlates with relapse and short overall survival in non-small cell lung cancer [68]

REM1

Moderate

Missense variant

c.188C>T

p.Pro63Leu

 

PCSK1

Moderate

Missense variant

c.1270C>G

p.Pro424Ala

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