Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RSPO2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276659
Start	107989129:107989129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.210G>T
AA Mutation	p.Gln70His(p.Q70H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000276659
Start	107989168:107989168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.171G>T
AA Mutation	p.Gln57His(p.Q57H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000276659
Start	107989148:107989148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182334537
CDS Mutation	c.191G>A
AA Mutation	p.Arg64Gln(p.R64Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000276659
Start	108082557:108082557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.82C>T
AA Mutation	p.Arg28Cys(p.R28C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000276659
Start	107958191:107958191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747227279
CDS Mutation	c.505C>A
AA Mutation	p.Leu169Met(p.L169M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000276659
Start	107989240:107989240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99T>G
AA Mutation	p.Ser33Arg(p.S33R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000276659
Start	108082582:108082582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768980014
CDS Mutation	c.57C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RSPO2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276659
Start	107960788:107960788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.313T>C
AA Mutation	p.Phe105Leu(p.F105L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000276659
Start	107958147:107958147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.549C>A
AA Mutation	p.Asp183Glu(p.D183E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000276659
Start	107989148:107989148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182334537
CDS Mutation	c.191G>A
AA Mutation	p.Arg64Gln(p.R64Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript