Colon Cancer: Gene >> CANX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000247461
Start	179722916:179722916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1295A>G
AA Mutation	p.Asp432Gly(p.D432G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000247461
Start	179709976:179709976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.632C>T
AA Mutation	p.Thr211Met(p.T211M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000247461
Start	179705827:179705827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.146C>T
AA Mutation	p.Thr49Ile(p.T49I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000247461
Start	179710043:179710043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.699G>T
AA Mutation	p.Lys233Asn(p.K233N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247461
Start	179719761:179719761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536838219
CDS Mutation	c.1005C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247461
Start	179706296:179706296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.210T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247461
Start	179705744:179705744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.63T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247461
Start	179710001:179710001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000247461
Start	179722918:179722919(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1305dupT
AA Mutation	p.Asp436Ter(p.D436*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CANX

No Mutation Annotation!