Colon Cancer: Gene >> CHIA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343320
Start	111312252:111312252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373325850
CDS Mutation	c.118C>T
AA Mutation	p.Arg40Cys(p.R40C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343320
Start	111320363:111320363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1328A>G
AA Mutation	p.Asn443Ser(p.N443S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343320
Start	111320425:111320425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1390C>T
AA Mutation	p.Leu464Phe(p.L464F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343320
Start	111312342:111312342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752677743
CDS Mutation	c.208G>A
AA Mutation	p.Glu70Lys(p.E70K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000343320
Start	111312238:111312238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746963750
CDS Mutation	c.104G>A
AA Mutation	p.Arg35Gln(p.R35Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000343320
Start	111312303:111312303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182022651
CDS Mutation	c.169G>A
AA Mutation	p.Ala57Thr(p.A57T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000343320
Start	111318020:111318020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640C>A
AA Mutation	p.Leu214Ile(p.L214I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000343320
Start	111320231:111320231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1196A>C
AA Mutation	p.Gln399Pro(p.Q399P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000343320
Start	111317726:111317726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526C>T
AA Mutation	p.Pro176Ser(p.P176S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343320
Start	111315285:111315285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.330T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343320
Start	111319135:111319135(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.935delA
AA Mutation	p.Asn312MetfsTer68(p.N312Mfs*68)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CHIA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343320
Start	111318634:111318634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549528699
CDS Mutation	c.871G>T
AA Mutation	p.Ala291Ser(p.A291S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343320
Start	111312341:111312341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767144908
CDS Mutation	c.207C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343320
Start	111318543:111318543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.780C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343320
Start	111320433:111320433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs544028644
CDS Mutation	c.1398C>T
Mutation Classification	Silent
Feature Type	Transcript