Colon Cancer: Gene >> LRCH4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310300
Start	100577863:100577863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191101243
CDS Mutation	c.998G>A
AA Mutation	p.Arg333Gln(p.R333Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310300
Start	100585979:100585979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.122C>T
AA Mutation	p.Ala41Val(p.A41V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310300
Start	100576964:100576964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375173199
CDS Mutation	c.1406C>T
AA Mutation	p.Ala469Val(p.A469V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310300
Start	100577378:100577378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769364186
CDS Mutation	c.1190C>T
AA Mutation	p.Pro397Leu(p.P397L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310300
Start	100577315:100577315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1253A>G
AA Mutation	p.Gln418Arg(p.Q418R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310300
Start	100577386:100577386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1182G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310300
Start	100577694:100577694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761154684
CDS Mutation	c.1086C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310300
Start	100578413:100578413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762768568
CDS Mutation	c.834G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LRCH4

No Mutation Annotation!