Colon Cancer: Gene >> SREBF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361204
Start	41880809:41880809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1855C>A
AA Mutation	p.Leu619Ile(p.L619I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361204
Start	41900463:41900463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370413839
CDS Mutation	c.2872G>A
AA Mutation	p.Val958Ile(p.V958I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361204
Start	41884884:41884884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2081C>T
AA Mutation	p.Ala694Val(p.A694V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361204
Start	41868701:41868701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.629G>A
AA Mutation	p.Arg210Gln(p.R210Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361204
Start	41866911:41866911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.169A>G
AA Mutation	p.Ser57Gly(p.S57G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361204
Start	41897143:41897143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151291415
CDS Mutation	c.2587G>A
AA Mutation	p.Val863Met(p.V863M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361204
Start	41877347:41877347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1505A>G
AA Mutation	p.Gln502Arg(p.Q502R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361204
Start	41867053:41867053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147075621
CDS Mutation	c.311C>T
AA Mutation	p.Ala104Val(p.A104V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361204
Start	41868767:41868767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.695C>A
AA Mutation	p.Ala232Asp(p.A232D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361204
Start	41875592:41875592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1254C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361204
Start	41897058:41897058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2502C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361204
Start	41903074:41903074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3012A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361204
Start	41870993:41870993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35259415
CDS Mutation	c.825C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361204
Start	41867033:41867033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.291A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361204
Start	41875559:41875559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560473946
CDS Mutation	c.1221C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361204
Start	41867240:41867240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.498G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000361204
Start	41873951:41873951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1021C>T
AA Mutation	p.Arg341Ter(p.R341*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000361204
Start	41866986:41866986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.244G>T
AA Mutation	p.Gly82Ter(p.G82*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361204
Start	41867058:41867059(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.320dupC
AA Mutation	p.Gln108ThrfsTer70(p.Q108Tfs*70)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SREBF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361204
Start	41884871:41884871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2068G>T
AA Mutation	p.Asp690Tyr(p.D690Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361204
Start	41897157:41897157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2601C>T
Mutation Classification	Silent
Feature Type	Transcript