Colon Cancer: Gene >> CYTH1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361101
Start	78680271:78680271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770347515
CDS Mutation	c.1037G>A
AA Mutation	p.Arg346Gln(p.R346Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361101
Start	78698346:78698346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.734A>C
AA Mutation	p.Lys245Thr(p.K245T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361101
Start	78680997:78680997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776237586
CDS Mutation	c.937C>T
AA Mutation	p.Arg313Trp(p.R313W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361101
Start	78702560:78702560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.215A>C
AA Mutation	p.Lys72Thr(p.K72T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361101
Start	78698879:78698880(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.639dupG
AA Mutation	p.Phe214ValfsTer10(p.F214Vfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361101
Start	78698351:78698352(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.728_729insTAAGTCTCAG
AA Mutation	p.Phe244LysfsTer5(p.F244Kfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CYTH1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361101
Start	78698269:78698269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778692007
CDS Mutation	c.811G>A
AA Mutation	p.Gly271Arg(p.G271R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361101
Start	78698965:78698965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.554C>A
AA Mutation	p.Thr185Asn(p.T185N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript