Colon Cancer: Gene >> SREBF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261646
Start	17820282:17820282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.331C>A
AA Mutation	p.Pro111Thr(p.P111T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261646
Start	17818307:17818307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1136A>T
AA Mutation	p.Lys379Ile(p.K379I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261646
Start	17819671:17819671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs568851975
CDS Mutation	c.578C>T
AA Mutation	p.Pro193Leu(p.P193L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261646
Start	17819669:17819669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.580C>T
AA Mutation	p.Pro194Ser(p.P194S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261646
Start	17820172:17820172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.441G>T
AA Mutation	p.Gln147His(p.Q147H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261646
Start	17819093:17819093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566513103
CDS Mutation	c.988G>A
AA Mutation	p.Ala330Thr(p.A330T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261646
Start	17814928:17814928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2509C>T
AA Mutation	p.Leu837Phe(p.L837F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261646
Start	17817282:17817282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1580G>A
AA Mutation	p.Arg527His(p.R527H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261646
Start	17817321:17817321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1541G>T
AA Mutation	p.Ser514Ile(p.S514I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261646
Start	17818281:17818281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754006664
CDS Mutation	c.1162C>T
AA Mutation	p.Arg388Cys(p.R388C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261646
Start	17816685:17816685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1819C>A
AA Mutation	p.Leu607Met(p.L607M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261646
Start	17815262:17815262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2451G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000261646
Start	17817375:17817392(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1470_1487delGTGCACGCTCGTCTTCCT
AA Mutation	p.Thr492_Cys497del(p.T492_C497del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SREBF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261646
Start	17816986:17816986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147642834
CDS Mutation	c.1757G>A
AA Mutation	p.Arg586His(p.R586H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261646
Start	17820270:17820270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776768645
CDS Mutation	c.343G>A
AA Mutation	p.Ala115Thr(p.A115T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript