Colon Cancer: Gene >> P2RY4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374519
Start	70258684:70258684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775064288
CDS Mutation	c.941G>A
AA Mutation	p.Arg314Gln(p.R314Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374519
Start	70259464:70259464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161C>G
AA Mutation	p.Ala54Gly(p.A54G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374519
Start	70258831:70258831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.794G>A
AA Mutation	p.Arg265His(p.R265H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374519
Start	70258891:70258891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778002771
CDS Mutation	c.734G>A
AA Mutation	p.Arg245His(p.R245H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374519
Start	70258673:70258673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775969220
CDS Mutation	c.952C>T
AA Mutation	p.Arg318Cys(p.R318C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374519
Start	70259033:70259033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.592G>T
AA Mutation	p.Val198Leu(p.V198L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374519
Start	70258994:70258994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201727833
CDS Mutation	c.631G>A
AA Mutation	p.Val211Met(p.V211M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374519
Start	70259290:70259290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375834423
CDS Mutation	c.335G>A
AA Mutation	p.Arg112His(p.R112H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374519
Start	70259227:70259227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.398G>A
AA Mutation	p.Arg133His(p.R133H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000374519
Start	70259429:70259429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.196C>A
AA Mutation	p.Pro66Thr(p.P66T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374519
Start	70258545:70258545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1080T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374519
Start	70259181:70259181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.444C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> P2RY4

No Mutation Annotation!