Colon Cancer: Gene >> NCAPG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356309
Start	158671578:158671578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199662183
CDS Mutation	c.1415C>T
AA Mutation	p.Ser472Leu(p.S472L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356309
Start	158692949:158692949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.275G>A
AA Mutation	p.Ser92Asn(p.S92N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356309
Start	158646515:158646515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3124C>T
AA Mutation	p.Pro1042Ser(p.P1042S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356309
Start	158680022:158680022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1084G>T
AA Mutation	p.Asp362Tyr(p.D362Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356309
Start	158664558:158664558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1672G>A
AA Mutation	p.Ala558Thr(p.A558T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356309
Start	158664713:158664713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753719449
CDS Mutation	c.1517G>A
AA Mutation	p.Arg506His(p.R506H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356309
Start	158652328:158652328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377006246
CDS Mutation	c.2899C>T
AA Mutation	p.Arg967Trp(p.R967W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356309
Start	158692919:158692919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305T>C
AA Mutation	p.Val102Ala(p.V102A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356309
Start	158693411:158693411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547669473
CDS Mutation	c.165G>T
AA Mutation	p.Lys55Asn(p.K55N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356309
Start	158675564:158675564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370565592
CDS Mutation	c.1239G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356309
Start	158680742:158680742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.999C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000356309
Start	158662313:158662313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1870G>T
AA Mutation	p.Glu624Ter(p.E624*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000356309
Start	158680720:158680720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1020+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NCAPG2

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000356309
Start	158689824:158689824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.667G>T
AA Mutation	p.Glu223Ter(p.E223*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript