Colon Cancer: Gene >> TRPC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000476941
Start	142784998:142784998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1255G>A
AA Mutation	p.Ala419Thr(p.A419T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000476941
Start	142791066:142791066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1345G>T
AA Mutation	p.Asp449Tyr(p.D449Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000476941
Start	142802169:142802169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1582A>C
AA Mutation	p.Ile528Leu(p.I528L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000476941
Start	142780976:142780976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.907G>A
AA Mutation	p.Glu303Lys(p.E303K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000476941
Start	142784900:142784900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157A>C
AA Mutation	p.Lys386Thr(p.K386T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000476941
Start	142806228:142806228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779282312
CDS Mutation	c.2375G>T
AA Mutation	p.Arg792Ile(p.R792I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000476941
Start	142736444:142736444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.238G>A
AA Mutation	p.Val80Ile(p.V80I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000476941
Start	142784873:142784873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1130G>A
AA Mutation	p.Gly377Asp(p.G377D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000476941
Start	142748271:142748271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539204792
CDS Mutation	c.443G>A
AA Mutation	p.Arg148Gln(p.R148Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000476941
Start	142784759:142784759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs569515062
CDS Mutation	c.1016T>A
AA Mutation	p.Met339Lys(p.M339K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000476941
Start	142806134:142806134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2281C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000476941
Start	142785006:142785006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1263A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000476941
Start	142791128:142791128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1407C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000476941
Start	142804065:142804065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1846G>T
AA Mutation	p.Glu616Ter(p.E616*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000476941
Start	142802345:142802345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1757+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TRPC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000476941
Start	142806168:142806168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2315G>A
AA Mutation	p.Arg772Gln(p.R772Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000476941
Start	142804054:142804054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1835G>C
AA Mutation	p.Ser612Thr(p.S612T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000476941
Start	142802220:142802220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1633C>A
AA Mutation	p.Leu545Ile(p.L545I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000476941
Start	142780980:142780980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.911G>T
AA Mutation	p.Arg304Ile(p.R304I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000476941
Start	142724619:142724619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.60T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000476941
Start	142736488:142736488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770645332
CDS Mutation	c.282C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000476941
Start	142804451:142804451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1975G>T
AA Mutation	p.Glu659Ter(p.E659*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript