Colon Cancer: Gene >> TRPC5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111912619:111912619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.572G>A
AA Mutation	p.Arg191His(p.R191H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111776511:111776511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2724A>C
AA Mutation	p.Glu908Asp(p.E908D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111847279:111847279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1535G>A
AA Mutation	p.Arg512His(p.R512H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111852342:111852342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1333C>T
AA Mutation	p.Leu445Phe(p.L445F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111835037:111835037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1780C>T
AA Mutation	p.His594Tyr(p.H594Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111912526:111912526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754729916
CDS Mutation	c.665G>A
AA Mutation	p.Arg222His(p.R222H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111776989:111776989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2246A>T
AA Mutation	p.Asp749Val(p.D749V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111912503:111912503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.688C>T
AA Mutation	p.Leu230Phe(p.L230F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111847280:111847280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747130444
CDS Mutation	c.1534C>T
AA Mutation	p.Arg512Cys(p.R512C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111776864:111776864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138566611
CDS Mutation	c.2371C>T
AA Mutation	p.Arg791Trp(p.R791W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111952209:111952209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.212G>A
AA Mutation	p.Arg71Gln(p.R71Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111952107:111952107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314G>A
AA Mutation	p.Arg105His(p.R105H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111912667:111912667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.524G>A
AA Mutation	p.Arg175His(p.R175H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111776783:111776783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2452C>T
AA Mutation	p.Pro818Ser(p.P818S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111782041:111782041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1994C>A
AA Mutation	p.Pro665His(p.P665H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111835100:111835100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1717C>A
AA Mutation	p.Gln573Lys(p.Q573K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111847345:111847345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749102820
CDS Mutation	c.1469C>T
AA Mutation	p.Ser490Leu(p.S490L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111776458:111776458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2777T>G
AA Mutation	p.Leu926Arg(p.L926R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111952315:111952315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.106T>A
AA Mutation	p.Phe36Ile(p.F36I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262839
Start	111835080:111835080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1737A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262839
Start	111776805:111776805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2430G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000262839
Start	111778996:111778996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2221G>T
AA Mutation	p.Glu741Ter(p.E741*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TRPC5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262839
Start	111912725:111912725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749694789
CDS Mutation	c.466G>A
AA Mutation	p.Glu156Lys(p.E156K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262839
Start	111952121:111952121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.300G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000262839
Start	111778983:111778983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2232+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript