Colon Cancer: Gene >> CA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377443
Start	8945908:8945908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.22C>A
AA Mutation	p.Leu8Met(p.L8M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377443
Start	8957265:8957265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.388G>T
AA Mutation	p.Gly130Trp(p.G130W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377443
Start	8967707:8967707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.620G>A
AA Mutation	p.Arg207Lys(p.R207K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377443
Start	8967665:8967665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.578G>T
AA Mutation	p.Arg193Ile(p.R193I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377443
Start	8957208:8957208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.331C>T
AA Mutation	p.His111Tyr(p.H111Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377443
Start	8967772:8967772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.685C>T
AA Mutation	p.His229Tyr(p.H229Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377443
Start	8949326:8949326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377435950
CDS Mutation	c.143C>T
AA Mutation	p.Ser48Leu(p.S48L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377443
Start	8962592:8962592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.507G>T
AA Mutation	p.Lys169Asn(p.K169N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000377443
Start	8967758:8967758(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.671G>A
AA Mutation	p.Cys224Tyr(p.C224Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377443
Start	8967750:8967750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144483907
CDS Mutation	c.663G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CA6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377443
Start	8967682:8967682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.595C>T
AA Mutation	p.Leu199Phe(p.L199F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript