Colon Cancer: Gene >> XPC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285021
Start	14148920:14148920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759032271
CDS Mutation	c.2144G>A
AA Mutation	p.Arg715Gln(p.R715Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285021
Start	14158887:14158887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.996G>T
AA Mutation	p.Lys332Asn(p.K332N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000285021
Start	14167206:14167206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584A>C
AA Mutation	p.Lys195Thr(p.K195T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000285021
Start	14164903:14164903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.810A>C
AA Mutation	p.Glu270Asp(p.E270D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000285021
Start	14156356:14156356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs3731140
CDS Mutation	c.2012G>A
AA Mutation	p.Arg671His(p.R671H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285021
Start	14147941:14147941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2481T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285021
Start	14147296:14147296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2598G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285021
Start	14158386:14158386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150344169
CDS Mutation	c.1497G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285021
Start	14170472:14170472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285021
Start	14158128:14158128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770336067
CDS Mutation	c.1755C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> XPC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000285021
Start	14172915:14172915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.251A>C
AA Mutation	p.Asn84Thr(p.N84T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000285021
Start	14170529:14170529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321G>T
AA Mutation	p.Lys107Asn(p.K107N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000285021
Start	14148617:14148617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2365G>T
AA Mutation	p.Asp789Tyr(p.D789Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000285021
Start	14158224:14158224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1659C>T
Mutation Classification	Silent
Feature Type	Transcript