Colon Cancer: Gene >> LYN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000519728
Start	55952094:55952094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759824481
CDS Mutation	c.616G>A
AA Mutation	p.Asp206Asn(p.D206N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000519728
Start	55999511:55999511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1298T>A
AA Mutation	p.Leu433Gln(p.L433Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000519728
Start	55999513:55999513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1300T>A
AA Mutation	p.Tyr434Asn(p.Y434N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000519728
Start	55998361:55998361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1066G>A
AA Mutation	p.Ala356Thr(p.A356T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000519728
Start	55951981:55951981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.503C>T
AA Mutation	p.Ser168Phe(p.S168F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000519728
Start	55951983:55951983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505G>A
AA Mutation	p.Val169Ile(p.V169I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000519728
Start	56009934:56009934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1363G>A
AA Mutation	p.Ala455Thr(p.A455T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000519728
Start	55966792:55966792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868G>A
AA Mutation	p.Glu290Lys(p.E290K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000519728
Start	56010063:56010063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1492G>T
AA Mutation	p.Asp498Tyr(p.D498Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000519728
Start	56010043:56010043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1472A>G
AA Mutation	p.Asp491Gly(p.D491G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000519728
Start	55953967:55953967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.773T>G
AA Mutation	p.Phe258Cys(p.F258C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000519728
Start	55999442:55999442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1229C>T
AA Mutation	p.Thr410Met(p.T410M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000519728
Start	55950495:55950495(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.327delA
AA Mutation	p.Glu110LysfsTer15(p.E110Kfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000519728
Start	55950559:55950559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.383+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> LYN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000519728
Start	55999421:55999421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1208C>G
AA Mutation	p.Ala403Gly(p.A403G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript