Colon Cancer: Gene >> TRPV2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338560
Start	16423748:16423748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.905C>T
AA Mutation	p.Ala302Val(p.A302V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338560
Start	16436809:16436809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2215C>A
AA Mutation	p.Leu739Met(p.L739M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338560
Start	16426160:16426160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.986C>A
AA Mutation	p.Thr329Asn(p.T329N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000338560
Start	16428335:16428335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1369C>T
AA Mutation	p.Arg457Cys(p.R457C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000338560
Start	16432238:16432238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1927G>A
AA Mutation	p.Ala643Thr(p.A643T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000338560
Start	16420146:16420146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.232C>T
AA Mutation	p.Arg78Trp(p.R78W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000338560
Start	16434961:16434961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547123940
CDS Mutation	c.2186G>A
AA Mutation	p.Gly729Asp(p.G729D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000338560
Start	16426111:16426111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.937A>G
AA Mutation	p.Ile313Val(p.I313V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338560
Start	16422672:16422672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.408G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338560
Start	16417674:16417674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338560
Start	16427521:16427521(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1329delG
AA Mutation	p.Ile444SerfsTer23(p.I444Sfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TRPV2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000338560
Start	16422600:16422600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.336G>T
AA Mutation	p.Glu112Asp(p.E112D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338560
Start	16420132:16420132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569542610
CDS Mutation	c.218G>A
AA Mutation	p.Arg73Gln(p.R73Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript