Colon Cancer: Gene >> GPR180

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376958
Start	94619177:94619177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.533T>C
AA Mutation	p.Val178Ala(p.V178A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376958
Start	94612373:94612373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.488T>G
AA Mutation	p.Phe163Cys(p.F163C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376958
Start	94619170:94619170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.526C>A
AA Mutation	p.Leu176Ile(p.L176I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376958
Start	94627041:94627041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754117607
CDS Mutation	c.1193A>G
AA Mutation	p.Gln398Arg(p.Q398R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376958
Start	94605459:94605459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.214T>C
AA Mutation	p.Tyr72His(p.Y72H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376958
Start	94619475:94619475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.694A>G
AA Mutation	p.Lys232Glu(p.K232E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376958
Start	94626030:94626030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1151A>G
AA Mutation	p.Tyr384Cys(p.Y384C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000376958
Start	94605456:94605456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.211C>A
AA Mutation	p.Leu71Ile(p.L71I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000376958
Start	94619201:94619201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.557G>A
AA Mutation	p.Cys186Tyr(p.C186Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376958
Start	94625981:94625981(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1106delT
AA Mutation	p.Leu369TyrfsTer24(p.L369Yfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GPR180

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376958
Start	94605418:94605418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.173T>A
AA Mutation	p.Ile58Asn(p.I58N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript