Colon Cancer: Gene >> SCFD1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000458591
Start	30707991:30707991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758690195
CDS Mutation	c.1555C>A
AA Mutation	p.Leu519Ile(p.L519I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000458591
Start	30653562:30653562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.829T>C
AA Mutation	p.Tyr277His(p.Y277H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000458591
Start	30707994:30707994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1558T>G
AA Mutation	p.Leu520Val(p.L520V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000458591
Start	30694774:30694774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1244C>A
AA Mutation	p.Ala415Glu(p.A415E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000458591
Start	30670395:30670395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.995G>A
AA Mutation	p.Ser332Asn(p.S332N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000458591
Start	30675043:30675043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1220C>T
AA Mutation	p.Thr407Ile(p.T407I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000458591
Start	30638132:30638132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561696273
CDS Mutation	c.320G>A
AA Mutation	p.Arg107Gln(p.R107Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000458591
Start	30719364:30719364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753170714
CDS Mutation	c.1723C>T
AA Mutation	p.Arg575Trp(p.R575W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000458591
Start	30622353:30622353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.15G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000458591
Start	30708036:30708036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1600G>T
AA Mutation	p.Gly534Ter(p.G534*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000458591
Start	30628249:30628250(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.107dupA
AA Mutation	p.Asn36LysfsTer14(p.N36Kfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000458591
Start	30643389:30643390(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.603dupT
AA Mutation	p.Val202CysfsTer43(p.V202Cfs*43)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SCFD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000458591
Start	30673331:30673331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1070G>A
AA Mutation	p.Arg357Gln(p.R357Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript