Colon Cancer: Gene >> GLP2R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262441
Start	9836394:9836394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.301G>T
AA Mutation	p.Asp101Tyr(p.D101Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262441
Start	9854534:9854534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.544T>C
AA Mutation	p.Tyr182His(p.Y182H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262441
Start	9887945:9887945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1298C>T
AA Mutation	p.Ala433Val(p.A433V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262441
Start	9870748:9870748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1058T>G
AA Mutation	p.Val353Gly(p.V353G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262441
Start	9857515:9857515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.704T>C
AA Mutation	p.Phe235Ser(p.F235S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262441
Start	9857482:9857482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.671G>T
AA Mutation	p.Arg224Ile(p.R224I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262441
Start	9880435:9880435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1203C>A
AA Mutation	p.Phe401Leu(p.F401L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262441
Start	9889505:9889505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1462G>A
AA Mutation	p.Glu488Lys(p.E488K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262441
Start	9889501:9889501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139614327
CDS Mutation	c.1458C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262441
Start	9862036:9862036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779122087
CDS Mutation	c.1002T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262441
Start	9860002:9860002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.826T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GLP2R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262441
Start	9889472:9889472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1429T>A
AA Mutation	p.Cys477Ser(p.C477S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262441
Start	9889619:9889619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1576C>T
AA Mutation	p.Arg526Trp(p.R526W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262441
Start	9842584:9842584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749983399
CDS Mutation	c.472G>A
AA Mutation	p.Glu158Lys(p.E158K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262441
Start	9857469:9857469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.658T>A
AA Mutation	p.Ser220Thr(p.S220T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262441
Start	9887967:9887967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563623280
CDS Mutation	c.1320T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262441
Start	9889582:9889582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1539G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262441
Start	9889486:9889486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763534036
CDS Mutation	c.1443C>T
Mutation Classification	Silent
Feature Type	Transcript