Colon Cancer: Gene >> GPR137

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313074
Start	64286741:64286741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.217C>T
AA Mutation	p.Arg73Cys(p.R73C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313074
Start	64289319:64289319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761684438
CDS Mutation	c.1208C>T
AA Mutation	p.Pro403Leu(p.P403L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313074
Start	64287786:64287786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.473C>T
AA Mutation	p.Ala158Val(p.A158V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000313074
Start	64286864:64286864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.340A>C
AA Mutation	p.Asn114His(p.N114H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313074
Start	64286587:64286587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.63T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313074
Start	64288159:64288159(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.733delC
AA Mutation	p.Gln245ArgfsTer21(p.Q245Rfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313074
Start	64289182:64289183(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1075dupC
AA Mutation	p.His359ProfsTer4(p.H359Pfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GPR137

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313074
Start	64289192:64289192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778003446
CDS Mutation	c.1081C>T
AA Mutation	p.Arg361Cys(p.R361C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313074
Start	64288206:64288206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.775T>C
AA Mutation	p.Ser259Pro(p.S259P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript