Colon Cancer: Gene >> AHSG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000411641
Start	186619866:186619866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.685T>G
AA Mutation	p.Phe229Val(p.F229V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000411641
Start	186620730:186620730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.904G>A
AA Mutation	p.Ala302Thr(p.A302T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000411641
Start	186620659:186620659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833C>A
AA Mutation	p.Pro278His(p.P278H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000411641
Start	186620679:186620679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766181399
CDS Mutation	c.853G>A
AA Mutation	p.Ala285Thr(p.A285T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000411641
Start	186620828:186620828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370801937
CDS Mutation	c.1002G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000411641
Start	186620678:186620678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762922913
CDS Mutation	c.852C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000411641
Start	186613231:186613231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142527838
CDS Mutation	c.90G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000411641
Start	186620600:186620600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000411641
Start	186618536:186618536(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.577delC
AA Mutation	p.Leu193SerfsTer53(p.L193Sfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000411641
Start	186619898:186619899(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.721dupG
AA Mutation	p.Ala241GlyfsTer26(p.A241Gfs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000411641
Start	186615684:186615684(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.214-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> AHSG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000411641
Start	186620901:186620901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1075C>G
AA Mutation	p.Pro359Ala(p.P359A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript