Colon Cancer: Gene >> CDC16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356221
Start	114242220:114242220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765036454
CDS Mutation	c.481G>A
AA Mutation	p.Val161Ile(p.V161I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356221
Start	114259379:114259379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1295T>A
AA Mutation	p.Ile432Asn(p.I432N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356221
Start	114272439:114272439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373980044
CDS Mutation	c.1859C>T
AA Mutation	p.Thr620Met(p.T620M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356221
Start	114243319:114243319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746190360
CDS Mutation	c.604C>T
AA Mutation	p.Arg202Cys(p.R202C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356221
Start	114272217:114272217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1637A>G
AA Mutation	p.Asp546Gly(p.D546G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356221
Start	114265207:114265207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1570G>A
AA Mutation	p.Glu524Lys(p.E524K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356221
Start	114272265:114272265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1685C>T
AA Mutation	p.Pro562Leu(p.P562L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356221
Start	114272319:114272319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1739T>G
AA Mutation	p.Leu580Arg(p.L580R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356221
Start	114262936:114262936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766838450
CDS Mutation	c.1434C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000356221
Start	114236882:114236882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771886807
CDS Mutation	c.187C>T
AA Mutation	p.Arg63Ter(p.R63*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CDC16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356221
Start	114239414:114239414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749424782
CDS Mutation	c.305G>T
AA Mutation	p.Arg102Ile(p.R102I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356221
Start	114259360:114259360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1276C>A
AA Mutation	p.Leu426Ile(p.L426I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356221
Start	114250648:114250648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1071C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356221
Start	114243333:114243333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.618G>A
Mutation Classification	Silent
Feature Type	Transcript