Colon Cancer: Gene >> HBS1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367837
Start	134997525:134997525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.671C>T
AA Mutation	p.Ala224Val(p.A224V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367837
Start	134997607:134997607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.589C>T
AA Mutation	p.Pro197Ser(p.P197S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367837
Start	134966462:134966462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1910A>G
AA Mutation	p.Lys637Arg(p.K637R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367837
Start	134969265:134969265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779153204
CDS Mutation	c.1871C>T
AA Mutation	p.Thr624Met(p.T624M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367837
Start	134986139:134986139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772074143
CDS Mutation	c.1350A>C
AA Mutation	p.Glu450Asp(p.E450D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367837
Start	134996922:134996922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.820A>G
AA Mutation	p.Ser274Gly(p.S274G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367837
Start	134966370:134966370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774407298
CDS Mutation	c.2002C>T
AA Mutation	p.Arg668Cys(p.R668C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367837
Start	135039764:135039764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777731477
CDS Mutation	c.239G>A
AA Mutation	p.Arg80His(p.R80H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367837
Start	135042109:135042109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.127T>C
AA Mutation	p.Ser43Pro(p.S43P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367837
Start	134978767:134978767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750402350
CDS Mutation	c.1709G>A
AA Mutation	p.Gly570Asp(p.G570D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367837
Start	135002815:135002815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139749814
CDS Mutation	c.458G>A
AA Mutation	p.Arg153Gln(p.R153Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367837
Start	134966416:134966416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1956T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367837
Start	134987726:134987726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1149A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367837
Start	134997611:134997611(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.585delA
AA Mutation	p.Gly196AspfsTer40(p.G196Dfs*40)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000367837
Start	134969293:134969293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1843C>T
AA Mutation	p.Arg615Ter(p.R615*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HBS1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367837
Start	134985388:134985388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1445G>A
AA Mutation	p.Arg482Gln(p.R482Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript