Colon Cancer: Gene >> HS6ST2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000370836
Start	132629091:132629091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.950A>T
AA Mutation	p.Asn317Ile(p.N317I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370836
Start	132628569:132628569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1472C>T
AA Mutation	p.Ala491Val(p.A491V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370836
Start	132628419:132628419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1622C>T
AA Mutation	p.Pro541Leu(p.P541L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370836
Start	132957067:132957067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.688G>A
AA Mutation	p.Val230Met(p.V230M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370836
Start	132957024:132957024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.731G>A
AA Mutation	p.Arg244His(p.R244H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370836
Start	132956832:132956832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.923G>A
AA Mutation	p.Arg308His(p.R308H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370836
Start	132628387:132628387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1654A>G
AA Mutation	p.Asn552Asp(p.N552D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000370836
Start	132957105:132957105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.650G>A
AA Mutation	p.Arg217His(p.R217H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370836
Start	132957080:132957080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.675C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370836
Start	132958342:132958342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370836
Start	132628418:132628418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1623G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370836
Start	132628554:132628554(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1487delT
AA Mutation	p.Leu496CysfsTer7(p.L496Cfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000370836
Start	132629068:132629068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.973C>T
AA Mutation	p.Arg325Ter(p.R325*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HS6ST2

No Mutation Annotation!