Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> LRRC15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347624
Start	194360719:194360719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372164095
CDS Mutation	c.325G>A
AA Mutation	p.Ala109Thr(p.A109T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000347624
Start	194359851:194359851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1193A>T
AA Mutation	p.Asn398Ile(p.N398I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000347624
Start	194360157:194360157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111979102
CDS Mutation	c.887G>A
AA Mutation	p.Arg296Gln(p.R296Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000347624
Start	194359692:194359692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1352C>A
AA Mutation	p.Pro451His(p.P451H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000347624
Start	194359714:194359714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1330A>G
AA Mutation	p.Arg444Gly(p.R444G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347624
Start	194359514:194359514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1530C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LRRC15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347624
Start	194360152:194360152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.892C>T
AA Mutation	p.Leu298Phe(p.L298F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000347624
Start	194359746:194359746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764147493
CDS Mutation	c.1298C>T
AA Mutation	p.Pro433Leu(p.P433L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000347624
Start	194360098:194360098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.946C>T
AA Mutation	p.Leu316Phe(p.L316F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript