Colon Cancer: Gene >> P2RY13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325602
Start	151328549:151328549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.507C>A
AA Mutation	p.Phe169Leu(p.F169L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325602
Start	151328919:151328919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.137T>C
AA Mutation	p.Val46Ala(p.V46A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325602
Start	151328037:151328037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1019G>A
AA Mutation	p.Ser340Asn(p.S340N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325602
Start	151328375:151328375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150366287
CDS Mutation	c.681T>G
AA Mutation	p.Phe227Leu(p.F227L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325602
Start	151328099:151328099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.957C>A
AA Mutation	p.Phe319Leu(p.F319L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325602
Start	151328027:151328027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1029T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325602
Start	151328276:151328276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780197468
CDS Mutation	c.780C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325602
Start	151328765:151328765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.291T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325602
Start	151328267:151328267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.789C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325602
Start	151328354:151328354(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.702delA
AA Mutation	p.Val235TyrfsTer81(p.V235Yfs*81)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> P2RY13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325602
Start	151328637:151328637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.419A>C
AA Mutation	p.Asp140Ala(p.D140A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325602
Start	151328068:151328068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200097493
CDS Mutation	c.988T>C
AA Mutation	p.Cys330Arg(p.C330R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325602
Start	151328149:151328149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.907C>A
AA Mutation	p.Leu303Ile(p.L303I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript