Colon Cancer: Gene >> HPR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000540303
Start	72076560:72076560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526G>C
AA Mutation	p.Glu176Gln(p.E176Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000540303
Start	72076901:72076901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.867G>T
AA Mutation	p.Gln289His(p.Q289H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000540303
Start	72074371:72074371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182745400
CDS Mutation	c.179G>A
AA Mutation	p.Arg60His(p.R60H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000540303
Start	72076388:72076388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.354G>T
AA Mutation	p.Gln118His(p.Q118H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000540303
Start	72076920:72076920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780251908
CDS Mutation	c.886G>A
AA Mutation	p.Asp296Asn(p.D296N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000540303
Start	72074289:72074289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201818109
CDS Mutation	c.97C>T
AA Mutation	p.Arg33Cys(p.R33C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000540303
Start	72076931:72076931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.897T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000540303
Start	72076539:72076539(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.509delA
AA Mutation	p.Lys170SerfsTer4(p.K170Sfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> HPR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000540303
Start	72076366:72076366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.332C>T
AA Mutation	p.Ala111Val(p.A111V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000540303
Start	72076430:72076430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746582404
CDS Mutation	c.396G>A
Mutation Classification	Silent
Feature Type	Transcript