Colon Cancer: Gene >> LCP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000323076
Start	46148434:46148434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779555319
CDS Mutation	c.896A>T
AA Mutation	p.Tyr299Phe(p.Y299F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323076
Start	46146994:46146994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1088A>G
AA Mutation	p.Asn363Ser(p.N363S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323076
Start	46142331:46142331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755322384
CDS Mutation	c.1463G>A
AA Mutation	p.Arg488His(p.R488H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000323076
Start	46158924:46158924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.130C>T
AA Mutation	p.Pro44Ser(p.P44S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000323076
Start	46156499:46156499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.430A>G
AA Mutation	p.Ile144Val(p.I144V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000323076
Start	46130896:46130896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534221736
CDS Mutation	c.1669G>A
AA Mutation	p.Asp557Asn(p.D557N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000323076
Start	46158906:46158906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148G>T
AA Mutation	p.Val50Leu(p.V50L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323076
Start	46148436:46148436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.894T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000323076
Start	46156449:46156449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.480C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_lost
Transcription ID	ENST00000323076
Start	46127591:46127591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1884A>C
AA Mutation	p.Ter628CysextTer14(p.*628Cext*14)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LCP1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000323076
Start	46134248:46134248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1505A>C
AA Mutation	p.Tyr502Ser(p.Y502S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000323076
Start	46158848:46158848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.206T>C
AA Mutation	p.Ile69Thr(p.I69T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000323076
Start	46146964:46146964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1118G>T
AA Mutation	p.Arg373Ile(p.R373I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000323076
Start	46134228:46134228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1525G>T
AA Mutation	p.Glu509Ter(p.E509*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript