Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> GPR101

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298110
Start	137030536:137030536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377596671
CDS Mutation	c.1139G>A
AA Mutation	p.Arg380His(p.R380H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298110
Start	137031383:137031383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.292C>T
AA Mutation	p.Pro98Ser(p.P98S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298110
Start	137030239:137030239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1436C>T
AA Mutation	p.Pro479Leu(p.P479L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000298110
Start	137030962:137030962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.713T>C
AA Mutation	p.Val238Ala(p.V238A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000298110
Start	137031170:137031170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505G>A
AA Mutation	p.Gly169Ser(p.G169S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000298110
Start	137031361:137031361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.314C>T
AA Mutation	p.Thr105Met(p.T105M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000298110
Start	137030346:137030346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1329C>A
AA Mutation	p.Phe443Leu(p.F443L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000298110
Start	137031238:137031238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.437G>A
AA Mutation	p.Arg146His(p.R146H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000298110
Start	137030537:137030537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751549000
CDS Mutation	c.1138C>T
AA Mutation	p.Arg380Cys(p.R380C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000298110
Start	137030168:137030168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751971846
CDS Mutation	c.1507G>A
AA Mutation	p.Asp503Asn(p.D503N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000298110
Start	137031123:137031123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.552G>T
AA Mutation	p.Met184Ile(p.M184I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298110
Start	137030316:137030316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1359C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298110
Start	137030442:137030442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1233C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298110
Start	137031534:137031534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.141C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298110
Start	137031453:137031453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.222C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000298110
Start	137031191:137031191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484C>T
AA Mutation	p.Gln162Ter(p.Q162*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000298110
Start	137031255:137031256(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.419dupC
AA Mutation	p.Ser141ValfsTer36(p.S141Vfs*36)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GPR101

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298110
Start	137031106:137031106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569C>T
AA Mutation	p.Pro190Leu(p.P190L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298110
Start	137031004:137031004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.671C>T
AA Mutation	p.Ala224Val(p.A224V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298110
Start	137031134:137031134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.541C>A
AA Mutation	p.Leu181Ile(p.L181I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298110
Start	137031105:137031105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.570C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298110
Start	137031546:137031546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298110
Start	137031669:137031669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298110
Start	137031348:137031348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.327C>T
Mutation Classification	Silent
Feature Type	Transcript