Colon Cancer: Gene >> CORO7

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000251166
Start	4357168:4357168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2685G>T
AA Mutation	p.Glu895Asp(p.E895D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000251166
Start	4364281:4364281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761999840
CDS Mutation	c.1270G>A
AA Mutation	p.Ala424Thr(p.A424T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000251166
Start	4408250:4408250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.234C>A
AA Mutation	p.Asp78Glu(p.D78E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000251166
Start	4358477:4358477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201255366
CDS Mutation	c.2347G>A
AA Mutation	p.Val783Ile(p.V783I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000251166
Start	4364632:4364632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748161669
CDS Mutation	c.1102G>A
AA Mutation	p.Asp368Asn(p.D368N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000251166
Start	4407555:4407555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766048891
CDS Mutation	c.433G>A
AA Mutation	p.Ala145Thr(p.A145T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000251166
Start	4358374:4358374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768577818
CDS Mutation	c.2450G>A
AA Mutation	p.Arg817Gln(p.R817Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000251166
Start	4364672:4364672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775838457
CDS Mutation	c.1062G>T
AA Mutation	p.Glu354Asp(p.E354D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000251166
Start	4358019:4358019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2542G>A
AA Mutation	p.Ala848Thr(p.A848T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000251166
Start	4359577:4359577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2153C>T
AA Mutation	p.Ala718Val(p.A718V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000251166
Start	4395302:4395302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200117600
CDS Mutation	c.602C>T
AA Mutation	p.Pro201Leu(p.P201L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251166
Start	4407526:4407526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150918473
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251166
Start	4364633:4364633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769559140
CDS Mutation	c.1101C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251166
Start	4365031:4365031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140738162
CDS Mutation	c.870G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251166
Start	4360337:4360337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199645423
CDS Mutation	c.2049C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251166
Start	4362703:4362703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769374019
CDS Mutation	c.1311G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251166
Start	4388578:4388578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.669C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251166
Start	4405500:4405500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753464714
CDS Mutation	c.555G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CORO7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000251166
Start	4361002:4361002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766836793
CDS Mutation	c.1858C>A
AA Mutation	p.Arg620Ser(p.R620S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000251166
Start	4405501:4405501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778533107
CDS Mutation	c.554C>T
AA Mutation	p.Thr185Met(p.T185M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript