Colon Cancer: Gene >> TRPV1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399756
Start	3571602:3571602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761226552
CDS Mutation	c.2269G>A
AA Mutation	p.Val757Met(p.V757M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399756
Start	3590990:3590990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.578C>T
AA Mutation	p.Ala193Val(p.A193V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399756
Start	3577650:3577650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1661A>G
AA Mutation	p.Tyr554Cys(p.Y554C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399756
Start	3589821:3589821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1030A>G
AA Mutation	p.Thr344Ala(p.T344A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399756
Start	3590317:3590317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.680A>C
AA Mutation	p.Asp227Ala(p.D227A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000399756
Start	3588306:3588306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533984481
CDS Mutation	c.1106A>G
AA Mutation	p.Lys369Arg(p.K369R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000399756
Start	3592130:3592130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372945414
CDS Mutation	c.221C>T
AA Mutation	p.Pro74Leu(p.P74L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000399756
Start	3590359:3590359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759486588
CDS Mutation	c.638G>A
AA Mutation	p.Arg213His(p.R213H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000399756
Start	3571536:3571536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200115926
CDS Mutation	c.2335C>T
AA Mutation	p.Arg779Trp(p.R779W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399756
Start	3589942:3589942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764482452
CDS Mutation	c.909G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399756
Start	3591067:3591067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs222748
CDS Mutation	c.501C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399756
Start	3588281:3588281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758831607
CDS Mutation	c.1131C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399756
Start	3591016:3591016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200555594
CDS Mutation	c.552G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399756
Start	3591064:3591064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202156842
CDS Mutation	c.504C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399756
Start	3573864:3573864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199510793
CDS Mutation	c.1872C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399756
Start	3592084:3592084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201144788
CDS Mutation	c.267C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000399756
Start	3590032:3590032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.819G>A
AA Mutation	p.Trp273Ter(p.W273*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TRPV1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399756
Start	3591024:3591024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544C>T
AA Mutation	p.Arg182Trp(p.R182W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399756
Start	3592312:3592312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201154250
CDS Mutation	c.39G>A
Mutation Classification	Silent
Feature Type	Transcript