Colon Cancer: Gene >> LYAR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343470
Start	4283708:4283708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.35C>T
AA Mutation	p.Ser12Leu(p.S12L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343470
Start	4274424:4274424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757496286
CDS Mutation	c.775G>A
AA Mutation	p.Ala259Thr(p.A259T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343470
Start	4274436:4274436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756569454
CDS Mutation	c.763C>T
AA Mutation	p.Arg255Cys(p.R255C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343470
Start	4281875:4281875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151107558
CDS Mutation	c.145G>A
AA Mutation	p.Val49Met(p.V49M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343470
Start	4281894:4281894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770633401
CDS Mutation	c.126C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343470
Start	4283731:4283731(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.12delT
AA Mutation	p.Phe4LeufsTer10(p.F4Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343470
Start	4273645:4273645(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.857delA
AA Mutation	p.Lys286ArgfsTer2(p.K286Rfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000343470
Start	4274745:4274745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.454C>T
AA Mutation	p.Gln152Ter(p.Q152*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343470
Start	4268580:4268581(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.954_955insGTACATT
AA Mutation	p.Leu319ValfsTer10(p.L319Vfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LYAR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343470
Start	4268608:4268608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.927C>A
AA Mutation	p.Phe309Leu(p.F309L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343470
Start	4283635:4283635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528236112
CDS Mutation	c.108C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343470
Start	4279468:4279468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.408C>A
Mutation Classification	Silent
Feature Type	Transcript