Colon Cancer: Gene >> LNPEP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231368
Start	96979735:96979735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617A>C
AA Mutation	p.Asn206Thr(p.N206T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000231368
Start	97022306:97022306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2383G>A
AA Mutation	p.Val795Ile(p.V795I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000231368
Start	97015036:97015036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2317G>A
AA Mutation	p.Asp773Asn(p.D773N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000231368
Start	96993128:96993128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1245G>T
AA Mutation	p.Lys415Asn(p.K415N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000231368
Start	97006497:97006497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2017T>G
AA Mutation	p.Leu673Val(p.L673V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000231368
Start	96986603:96986603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1064G>A
AA Mutation	p.Ser355Asn(p.S355N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000231368
Start	96993129:96993129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1246A>C
AA Mutation	p.Lys416Gln(p.K416Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000231368
Start	97024607:97024607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2648C>A
AA Mutation	p.Ser883Tyr(p.S883Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000231368
Start	97006192:97006192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1905C>A
AA Mutation	p.Phe635Leu(p.F635L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000231368
Start	96998036:96998036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750360079
CDS Mutation	c.1544G>A
AA Mutation	p.Arg515Gln(p.R515Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231368
Start	96979337:96979337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.219A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231368
Start	97013718:97013718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2106A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231368
Start	96996473:96996473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1491T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000231368
Start	96979545:96979545(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.434delA
AA Mutation	p.Asn145ThrfsTer6(p.N145Tfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000231368
Start	96996478:96996478(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1501delA
AA Mutation	p.Ile501TyrfsTer12(p.I501Yfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000231368
Start	97024563:97024563(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2608delA
AA Mutation	p.Thr870LeufsTer15(p.T870Lfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000231368
Start	97022347:97022347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2424G>A
AA Mutation	p.Trp808Ter(p.W808*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000231368
Start	97013794:97013794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2182C>T
AA Mutation	p.Arg728Ter(p.R728*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LNPEP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231368
Start	97024585:97024585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2626T>A
AA Mutation	p.Phe876Ile(p.F876I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000231368
Start	96998023:96998023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1531T>G
AA Mutation	p.Phe511Val(p.F511V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000231368
Start	96979188:96979188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.70G>T
AA Mutation	p.Glu24Ter(p.E24*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript