Colon Cancer: Gene >> LMBR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000353442
Start	156725521:156725521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1072C>A
AA Mutation	p.Leu358Ile(p.L358I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000353442
Start	156836821:156836821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.131G>T
AA Mutation	p.Arg44Ile(p.R44I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000353442
Start	156836856:156836856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.96C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000353442
Start	156684153:156684153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1398A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000353442
Start	156688088:156688088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1329A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LMBR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000353442
Start	156688035:156688035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1382C>T
AA Mutation	p.Ala461Val(p.A461V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000353442
Start	156688048:156688048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1369G>A
AA Mutation	p.Glu457Lys(p.E457K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript