Colon Cancer: Gene >> HAS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222115
Start	51713819:51713819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1345G>A
AA Mutation	p.Ala449Thr(p.A449T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222115
Start	51719714:51719714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.194C>T
AA Mutation	p.Ala65Val(p.A65V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222115
Start	51717161:51717161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.735G>T
AA Mutation	p.Met245Ile(p.M245I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222115
Start	51719262:51719262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.646C>T
AA Mutation	p.Arg216Cys(p.R216C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000222115
Start	51713902:51713902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1262G>A
AA Mutation	p.Arg421His(p.R421H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000222115
Start	51719211:51719211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775182179
CDS Mutation	c.697G>A
AA Mutation	p.Val233Met(p.V233M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000222115
Start	51716299:51716299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191873019
CDS Mutation	c.1018C>T
AA Mutation	p.Arg340Trp(p.R340W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000222115
Start	51713494:51713494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1670C>T
AA Mutation	p.Thr557Met(p.T557M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000222115
Start	51713890:51713890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777058982
CDS Mutation	c.1274C>T
AA Mutation	p.Ala425Val(p.A425V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000222115
Start	51719222:51719222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.686C>T
AA Mutation	p.Ser229Leu(p.S229L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000222115
Start	51717068:51717068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.828G>T
AA Mutation	p.Trp276Cys(p.W276C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000222115
Start	51713441:51713441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372838640
CDS Mutation	c.1723C>T
AA Mutation	p.Arg575Cys(p.R575C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000222115
Start	51716289:51716289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765536727
CDS Mutation	c.1028C>T
AA Mutation	p.Thr343Ile(p.T343I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222115
Start	51719212:51719212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774926345
CDS Mutation	c.696C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222115
Start	51713967:51713967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759300669
CDS Mutation	c.1197G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222115
Start	51713769:51713769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1395G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222115
Start	51713727:51713727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1437G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HAS1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222115
Start	51714085:51714085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768198571
CDS Mutation	c.1079G>A
AA Mutation	p.Arg360His(p.R360H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222115
Start	51719269:51719269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222115
Start	51719230:51719230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.678C>T
Mutation Classification	Silent
Feature Type	Transcript