Colon Cancer: Gene >> HCK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000534862
Start	32052470:32052470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.46G>A
AA Mutation	p.Glu16Lys(p.E16K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000534862
Start	32099048:32099048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1291T>G
AA Mutation	p.Phe431Val(p.F431V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000534862
Start	32086685:32086685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.893C>T
AA Mutation	p.Ser298Leu(p.S298L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000534862
Start	32099060:32099060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1303A>G
AA Mutation	p.Thr435Ala(p.T435A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000534862
Start	32074698:32074698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.405C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000534862
Start	32099119:32099119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1362C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000534862
Start	32084536:32084536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.828C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000534862
Start	32093937:32093937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1167C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000534862
Start	32093937:32093937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1167C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000534862
Start	32083993:32083993(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.637delC
AA Mutation	p.Arg213GlufsTer77(p.R213Efs*77)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000534862
Start	32099116:32099116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1359C>G
AA Mutation	p.Tyr453Ter(p.Y453*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000534862
Start	32083998:32083998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144393224
CDS Mutation	c.637C>T
AA Mutation	p.Arg213Ter(p.R213*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000534862
Start	32052426:32052427(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs755024531
CDS Mutation	c.9dupG
AA Mutation	p.Arg4AlafsTer38(p.R4Afs*38)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HCK

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000534862
Start	32099107:32099107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs541906170
CDS Mutation	c.1350C>T
Mutation Classification	Silent
Feature Type	Transcript