Colon Cancer: Gene >> GPR75

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394705
Start	53854638:53854638(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.119C>G
AA Mutation	p.Ala40Gly(p.A40G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394705
Start	53854392:53854392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.365A>T
AA Mutation	p.His122Leu(p.H122L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394705
Start	53853211:53853211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1546C>T
AA Mutation	p.His516Tyr(p.H516Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394705
Start	53853624:53853624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765250002
CDS Mutation	c.1133G>A
AA Mutation	p.Arg378Gln(p.R378Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394705
Start	53854629:53854629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.128T>G
AA Mutation	p.Val43Gly(p.V43G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000394705
Start	53853574:53853574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1183G>A
AA Mutation	p.Gly395Ser(p.G395S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000394705
Start	53854375:53854375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.382T>C
AA Mutation	p.Phe128Leu(p.F128L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394705
Start	53854025:53854025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559738797
CDS Mutation	c.732C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394705
Start	53854712:53854712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528110151
CDS Mutation	c.45G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394705
Start	53853815:53853815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.942C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000394705
Start	53853853:53853853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376986894
CDS Mutation	c.904C>T
AA Mutation	p.Arg302Ter(p.R302*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394705
Start	53854459:53854460(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.297dupC
AA Mutation	p.Met100HisfsTer13(p.M100Hfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GPR75

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394705
Start	53853511:53853511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778576313
CDS Mutation	c.1246G>A
AA Mutation	p.Glu416Lys(p.E416K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394705
Start	53854014:53854014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743G>A
AA Mutation	p.Arg248Lys(p.R248K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394705
Start	53854291:53854291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.466G>A
AA Mutation	p.Ala156Thr(p.A156T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394705
Start	53854547:53854547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.210A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394705
Start	53853560:53853561(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1196dupT
AA Mutation	p.Cys400LeufsTer27(p.C400Lfs*27)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript