Colon Cancer: Gene >> LTF

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000231751
Start	46459657:46459657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765686239
CDS Mutation	c.206C>T
AA Mutation	p.Ala69Val(p.A69V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000231751
Start	46455840:46455840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148123129
CDS Mutation	c.455G>A
AA Mutation	p.Arg152His(p.R152H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000231751
Start	46459718:46459718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776865450
CDS Mutation	c.145C>T
AA Mutation	p.Arg49Cys(p.R49C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000231751
Start	46450003:46450003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200379115
CDS Mutation	c.908C>T
AA Mutation	p.Pro303Leu(p.P303L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000231751
Start	46441445:46441445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1694A>G
AA Mutation	p.Lys565Arg(p.K565R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000231751
Start	46437976:46437976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2062G>A
AA Mutation	p.Ala688Thr(p.A688T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000231751
Start	46438075:46438075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1963T>C
AA Mutation	p.Ser655Pro(p.S655P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000231751
Start	46445353:46445353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754476078
CDS Mutation	c.1441G>A
AA Mutation	p.Ala481Thr(p.A481T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231751
Start	46448923:46448923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138970012
CDS Mutation	c.1152C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231751
Start	46437977:46437977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372223957
CDS Mutation	c.2061C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231751
Start	46439371:46439371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1833C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231751
Start	46445315:46445315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1479C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231751
Start	46448989:46448989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61740472
CDS Mutation	c.1086G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000231751
Start	46450628:46450628(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.749delG
AA Mutation	p.Cys250SerfsTer30(p.C250Sfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LTF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000231751
Start	46455934:46455934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371681789
CDS Mutation	c.361G>A
AA Mutation	p.Gly121Ser(p.G121S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000231751
Start	46450021:46450021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.890T>C
AA Mutation	p.Phe297Ser(p.F297S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000231751
Start	46437959:46437959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2079G>A
Mutation Classification	Silent
Feature Type	Transcript