Colon Cancer: Gene >> MSLN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000382862
Start	766455:766455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1195C>T
AA Mutation	p.Leu399Phe(p.L399F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000382862
Start	765715:765715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759331194
CDS Mutation	c.820C>T
AA Mutation	p.Arg274Cys(p.R274C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000382862
Start	764954:764954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147793202
CDS Mutation	c.428G>A
AA Mutation	p.Arg143His(p.R143H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000382862
Start	766651:766651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751744116
CDS Mutation	c.1238G>A
AA Mutation	p.Arg413Gln(p.R413Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000382862
Start	766765:766765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1352C>A
AA Mutation	p.Ser451Tyr(p.S451Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000382862
Start	765778:765778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199964761
CDS Mutation	c.883C>T
AA Mutation	p.Arg295Trp(p.R295W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000382862
Start	765117:765117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201139558
CDS Mutation	c.518G>A
AA Mutation	p.Arg173Gln(p.R173Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000382862
Start	766104:766104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.941G>A
AA Mutation	p.Ser314Asn(p.S314N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000382862
Start	764713:764713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.367C>A
AA Mutation	p.Leu123Met(p.L123M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000382862
Start	766486:766486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1226C>A
AA Mutation	p.Pro409His(p.P409H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000382862
Start	765170:765170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145025982
CDS Mutation	c.571G>A
AA Mutation	p.Asp191Asn(p.D191N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382862
Start	764679:764679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.333C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000382862
Start	766933:766933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200796355
CDS Mutation	c.1446C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MSLN

No Mutation Annotation!