Colon Cancer: Gene >> LYVE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256178
Start	10559186:10559186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.894G>T
AA Mutation	p.Lys298Asn(p.K298N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256178
Start	10559271:10559271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.809A>G
AA Mutation	p.Asn270Ser(p.N270S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256178
Start	10559214:10559214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746141063
CDS Mutation	c.866A>G
AA Mutation	p.Asn289Ser(p.N289S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000256178
Start	10564317:10564317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141249676
CDS Mutation	c.143C>T
AA Mutation	p.Ala48Val(p.A48V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000256178
Start	10560645:10560645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749336203
CDS Mutation	c.553C>A
AA Mutation	p.Pro185Thr(p.P185T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000256178
Start	10559133:10559133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.947G>A
AA Mutation	p.Arg316Gln(p.R316Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000256178
Start	10559134:10559134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775409214
CDS Mutation	c.946C>T
AA Mutation	p.Arg316Ter(p.R316*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256178
Start	10560603:10560604(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.594dupA
AA Mutation	p.Leu199IlefsTer12(p.L199Ifs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LYVE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256178
Start	10560605:10560605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.593A>C
AA Mutation	p.Lys198Thr(p.K198T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript