Colon Cancer: Gene >> LIMK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336180
Start	74115896:74115896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1505A>G
AA Mutation	p.Asp502Gly(p.D502G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336180
Start	74121018:74121018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782109144
CDS Mutation	c.1750G>A
AA Mutation	p.Val584Met(p.V584M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336180
Start	74097146:74097146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.358G>T
AA Mutation	p.Asp120Tyr(p.D120Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336180
Start	74121194:74121194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368807700
CDS Mutation	c.1837G>A
AA Mutation	p.Gly613Ser(p.G613S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336180
Start	74111696:74111696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141412371
CDS Mutation	c.1333G>A
AA Mutation	p.Ala445Thr(p.A445T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336180
Start	74099066:74099066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544200500
CDS Mutation	c.436G>A
AA Mutation	p.Val146Ile(p.V146I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000336180
Start	74107908:74107908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1103A>C
AA Mutation	p.Lys368Thr(p.K368T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000336180
Start	74108918:74108918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1166G>A
AA Mutation	p.Arg389Gln(p.R389Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000336180
Start	74107123:74107123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781956388
CDS Mutation	c.995G>A
AA Mutation	p.Arg332His(p.R332H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336180
Start	74099116:74099116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.486C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336180
Start	74121200:74121200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1843C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000336180
Start	74115853:74115855(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1462_1464delGAG
AA Mutation	p.Glu488del(p.E488del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LIMK1

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000336180
Start	74121166:74121166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1809G>A
AA Mutation	p.Trp603Ter(p.W603*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript