Colon Cancer: Gene >> F10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375559
Start	113149137:113149137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1087G>A
AA Mutation	p.Gly363Ser(p.G363S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375559
Start	113148952:113148952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145282353
CDS Mutation	c.902C>T
AA Mutation	p.Ala301Val(p.A301V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375559
Start	113129523:113129523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.142A>G
AA Mutation	p.Met48Val(p.M48V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375559
Start	113129541:113129541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121964939
CDS Mutation	c.160G>A
AA Mutation	p.Glu54Lys(p.E54K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375559
Start	113149326:113149326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770671957
CDS Mutation	c.1276C>T
AA Mutation	p.Arg426Cys(p.R426C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375559
Start	113149114:113149114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1064C>T
AA Mutation	p.Thr355Met(p.T355M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000375559
Start	113144037:113144037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.689A>G
AA Mutation	p.Asn230Ser(p.N230S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000375559
Start	113129488:113129488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.107C>T
AA Mutation	p.Ala36Val(p.A36V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375559
Start	113144020:113144020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.672G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375559
Start	113148944:113148944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778741024
CDS Mutation	c.894C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375559
Start	113149202:113149202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371569721
CDS Mutation	c.1152C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375559
Start	113139448:113139448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747030511
CDS Mutation	c.348C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375559
Start	113143974:113143975(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.630dupC
AA Mutation	p.Thr211HisfsTer9(p.T211Hfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> F10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375559
Start	113139449:113139449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349G>A
AA Mutation	p.Glu117Lys(p.E117K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375559
Start	113139375:113139375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.275C>G
AA Mutation	p.Thr92Ser(p.T92S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375559
Start	113144016:113144016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566300775
CDS Mutation	c.668C>T
AA Mutation	p.Thr223Met(p.T223M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375559
Start	113140936:113140936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.388A>G
AA Mutation	p.Ser130Gly(p.S130G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375559
Start	113140962:113140962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.414G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375559
Start	113149013:113149013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148209958
CDS Mutation	c.963C>T
Mutation Classification	Silent
Feature Type	Transcript