Colon Cancer: Gene >> LSS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356396
Start	46215736:46215736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841G>A
AA Mutation	p.Ala281Thr(p.A281T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356396
Start	46210714:46210714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762530682
CDS Mutation	c.1168G>A
AA Mutation	p.Ala390Thr(p.A390T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356396
Start	46215257:46215257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764497439
CDS Mutation	c.934C>T
AA Mutation	p.Arg312Trp(p.R312W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000356396
Start	46208251:46208251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1317G>T
AA Mutation	p.Lys439Asn(p.K439N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356396
Start	46207538:46207538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1357G>A
AA Mutation	p.Val453Ile(p.V453I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356396
Start	46222672:46222672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200708561
CDS Mutation	c.386G>A
AA Mutation	p.Arg129Gln(p.R129Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356396
Start	46207547:46207547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375698498
CDS Mutation	c.1348G>A
AA Mutation	p.Gly450Ser(p.G450S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356396
Start	46219481:46219481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.642G>T
AA Mutation	p.Glu214Asp(p.E214D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356396
Start	46216423:46216423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.749C>T
AA Mutation	p.Ala250Val(p.A250V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356396
Start	46221897:46221897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757467514
CDS Mutation	c.507C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356396
Start	46205886:46205886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138736346
CDS Mutation	c.1620G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> LSS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356396
Start	46206716:46206716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199896537
CDS Mutation	c.1520G>A
AA Mutation	p.Arg507His(p.R507H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356396
Start	46191155:46191155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372838581
CDS Mutation	c.2148C>T
Mutation Classification	Silent
Feature Type	Transcript