Colon Cancer: Gene >> LCP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000046794
Start	170253207:170253207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157G>A
AA Mutation	p.Ser386Asn(p.S386N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000046794
Start	170248775:170248775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1524G>T
AA Mutation	p.Met508Ile(p.M508I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000046794
Start	170297586:170297586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26G>A
AA Mutation	p.Arg9His(p.R9H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000046794
Start	170262731:170262731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.830A>T
AA Mutation	p.Glu277Val(p.E277V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000046794
Start	170250860:170250860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1349G>A
AA Mutation	p.Ser450Asn(p.S450N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000046794
Start	170253138:170253138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1226C>A
AA Mutation	p.Pro409Gln(p.P409Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000046794
Start	170250747:170250747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1462G>C
AA Mutation	p.Gly488Arg(p.G488R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000046794
Start	170250766:170250766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1443A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000046794
Start	170253128:170253128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373084459
CDS Mutation	c.1236G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000046794
Start	170270801:170270801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369364060
CDS Mutation	c.441G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000046794
Start	170261112:170261112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.952G>T
AA Mutation	p.Glu318Ter(p.E318*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000046794
Start	170258096:170258097(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1040_1041insCTAAACATTATAT
AA Mutation	p.Lys348Ter(p.K348*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000046794
Start	170250848:170250849(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1360dupA
AA Mutation	p.Thr454AsnfsTer15(p.T454Nfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000046794
Start	170287969:170287969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.188+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> LCP2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000046794
Start	170266863:170266863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761168311
CDS Mutation	c.717G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000046794
Start	170275343:170275343(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.263delT
AA Mutation	p.Val88AlafsTer148(p.V88Afs*148)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript