Colon Cancer: Gene >> CBLN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269503
Start	72538183:72538183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.668C>A
AA Mutation	p.Pro223His(p.P223H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269503
Start	72538201:72538201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.650C>T
AA Mutation	p.Ser217Leu(p.S217L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269503
Start	72538237:72538237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614G>A
AA Mutation	p.Gly205Asp(p.G205D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269503
Start	72538280:72538280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571C>T
AA Mutation	p.Leu191Phe(p.L191F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000269503
Start	72541940:72541940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.221C>T
AA Mutation	p.Ala74Val(p.A74V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269503
Start	72541945:72541945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.216G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269503
Start	72538709:72538710(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.420dupA
AA Mutation	p.Gly141ArgfsTer4(p.G141Rfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CBLN2

No Mutation Annotation!