Colon Cancer: Gene >> LIMD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273317
Start	45672777:45672777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751216668
CDS Mutation	c.1729G>A
AA Mutation	p.Val577Met(p.V577M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273317
Start	45595240:45595240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361G>A
AA Mutation	p.Ala121Thr(p.A121T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000273317
Start	45596234:45596234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1355T>A
AA Mutation	p.Leu452His(p.L452H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000273317
Start	45595724:45595724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.845A>G
AA Mutation	p.Asn282Ser(p.N282S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000273317
Start	45595331:45595331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.452G>A
AA Mutation	p.Arg151Lys(p.R151K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273317
Start	45595425:45595425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.546C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273317
Start	45595302:45595302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754205344
CDS Mutation	c.423G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000273317
Start	45595833:45595833(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.959delG
AA Mutation	p.Gly320ValfsTer6(p.G320Vfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000273317
Start	45595874:45595875(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1000dupC
AA Mutation	p.Gln334ProfsTer65(p.Q334Pfs*65)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LIMD1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273317
Start	45595602:45595602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.723G>A
Mutation Classification	Silent
Feature Type	Transcript