Colon Cancer: Gene >> NCK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233154
Start	105881937:105881937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780151498
CDS Mutation	c.836G>A
AA Mutation	p.Arg279His(p.R279H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233154
Start	105893075:105893075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750135733
CDS Mutation	c.1042C>T
AA Mutation	p.Arg348Cys(p.R348C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000233154
Start	105855106:105855106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768027105
CDS Mutation	c.43G>A
AA Mutation	p.Ala15Thr(p.A15T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000233154
Start	105881927:105881927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.826T>C
AA Mutation	p.Ser276Pro(p.S276P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000233154
Start	105881693:105881693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766993432
CDS Mutation	c.592C>T
AA Mutation	p.His198Tyr(p.H198Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233154
Start	105881461:105881461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199727155
CDS Mutation	c.360C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233154
Start	105855207:105855207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.144G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233154
Start	105881926:105881926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756202194
CDS Mutation	c.825G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233154
Start	105855274:105855274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.211C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NCK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233154
Start	105881357:105881357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.256G>A
AA Mutation	p.Ala86Thr(p.A86T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233154
Start	105882041:105882041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.940G>A
AA Mutation	p.Glu314Lys(p.E314K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript