Colon Cancer: Gene >> GPR78

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382487
Start	8582551:8582551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.689T>C
AA Mutation	p.Ile230Thr(p.I230T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382487
Start	8587143:8587143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61741001
CDS Mutation	c.872C>T
AA Mutation	p.Pro291Leu(p.P291L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382487
Start	8587176:8587176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368485565
CDS Mutation	c.905G>A
AA Mutation	p.Arg302His(p.R302H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000382487
Start	8581200:8581200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218C>T
AA Mutation	p.Pro73Leu(p.P73L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000382487
Start	8582592:8582592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730G>T
AA Mutation	p.Gly244Cys(p.G244C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000382487
Start	8581271:8581271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754162901
CDS Mutation	c.289G>A
AA Mutation	p.Val97Met(p.V97M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000382487
Start	8581260:8581260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.278C>T
AA Mutation	p.Ala93Val(p.A93V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382487
Start	8587150:8587150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546309729
CDS Mutation	c.879G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382487
Start	8587318:8587318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1047C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382487
Start	8582582:8582582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.720C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382487
Start	8587066:8587066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779541119
CDS Mutation	c.795C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382487
Start	8581051:8581051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765752843
CDS Mutation	c.69C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> GPR78

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382487
Start	8581000:8581000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.18G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382487
Start	8582630:8582630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138639661
CDS Mutation	c.768G>A
Mutation Classification	Silent
Feature Type	Transcript