Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CNTFR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000351266
Start	34564746:34564746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767106678
CDS Mutation	c.172C>T
AA Mutation	p.Arg58Trp(p.R58W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000351266
Start	34556290:34556290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.733C>T
AA Mutation	p.Arg245Cys(p.R245C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000351266
Start	34564757:34564757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758772223
CDS Mutation	c.161C>T
AA Mutation	p.Ala54Val(p.A54V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000351266
Start	34552249:34552249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1030G>A
AA Mutation	p.Gly344Arg(p.G344R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000351266
Start	34568933:34568933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49G>A
AA Mutation	p.Ala17Thr(p.A17T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000351266
Start	34556274:34556274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.749T>C
AA Mutation	p.Ile250Thr(p.I250T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000351266
Start	34564738:34564738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.180T>G
AA Mutation	p.Asn60Lys(p.N60K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000351266
Start	34556277:34556277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.746T>A
AA Mutation	p.Leu249His(p.L249H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351266
Start	34552193:34552193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199588359
CDS Mutation	c.1086C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351266
Start	34557569:34557569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.561G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351266
Start	34552172:34552172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1107T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000351266
Start	34564680:34564680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.238G>T
AA Mutation	p.Glu80Ter(p.E80*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000351266
Start	34564739:34564740(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.178_179insCAGGA
AA Mutation	p.Asn60ThrfsTer86(p.N60Tfs*86)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CNTFR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000351266
Start	34564625:34564625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.293G>A
AA Mutation	p.Arg98His(p.R98H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000351266
Start	34552810:34552810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202050719
CDS Mutation	c.813C>T
Mutation Classification	Silent
Feature Type	Transcript