Colon Cancer: Gene >> TRPV3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000576742
Start	3513941:3513941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2349G>T
AA Mutation	p.Glu783Asp(p.E783D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000576742
Start	3542677:3542677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374241773
CDS Mutation	c.488C>T
AA Mutation	p.Thr163Met(p.T163M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000576742
Start	3518584:3518584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746084220
CDS Mutation	c.2077C>T
AA Mutation	p.Arg693Cys(p.R693C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000576742
Start	3554759:3554759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146728389
CDS Mutation	c.92C>T
AA Mutation	p.Pro31Leu(p.P31L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000576742
Start	3532931:3532931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs4790513
CDS Mutation	c.791C>T
AA Mutation	p.Thr264Met(p.T264M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000576742
Start	3516523:3516523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2132T>C
AA Mutation	p.Leu711Pro(p.L711P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000576742
Start	3526878:3526878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1553C>T
AA Mutation	p.Ser518Leu(p.S518L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000576742
Start	3532862:3532862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200272068
CDS Mutation	c.860C>T
AA Mutation	p.Thr287Met(p.T287M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000576742
Start	3544609:3544609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.281C>T
AA Mutation	p.Thr94Ile(p.T94I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000576742
Start	3518596:3518596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2065G>A
AA Mutation	p.Glu689Lys(p.E689K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000576742
Start	3543586:3543586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.354G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000576742
Start	3532930:3532930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765991862
CDS Mutation	c.792G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000576742
Start	3528118:3528118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374035465
CDS Mutation	c.1410G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000576742
Start	3532849:3532849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141405698
CDS Mutation	c.873G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TRPV3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000576742
Start	3545255:3545255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.136G>C
AA Mutation	p.Glu46Gln(p.E46Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000576742
Start	3524339:3524339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1602A>G
AA Mutation	p.Ile534Met(p.I534M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000576742
Start	3532766:3532766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151284467
CDS Mutation	c.956G>A
AA Mutation	p.Arg319His(p.R319H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000576742
Start	3528100:3528100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763235764
CDS Mutation	c.1428G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000576742
Start	3524305:3524305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1636G>T
AA Mutation	p.Glu546Ter(p.E546*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript