Colon Cancer: Gene >> KRT16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301653
Start	41611696:41611696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547733077
CDS Mutation	c.557C>T
AA Mutation	p.Ala186Val(p.A186V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301653
Start	41612603:41612603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.86G>A
AA Mutation	p.Ser29Asn(p.S29N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301653
Start	41611151:41611151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146562738
CDS Mutation	c.851G>A
AA Mutation	p.Arg284His(p.R284H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301653
Start	41612667:41612667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.22T>C
AA Mutation	p.Phe8Leu(p.F8L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301653
Start	41612616:41612616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.73G>T
AA Mutation	p.Gly25Trp(p.G25W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301653
Start	41612533:41612533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.156C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301653
Start	41612545:41612545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301653
Start	41610495:41610495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1116G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301653
Start	41612492:41612492(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.197delG
AA Mutation	p.Gly66AlafsTer54(p.G66Afs*54)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KRT16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301653
Start	41612589:41612589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530326477
CDS Mutation	c.100G>A
AA Mutation	p.Val34Ile(p.V34I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript