Colon Cancer: Gene >> ZDHHC5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287169
Start	57698809:57698809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1373G>T
AA Mutation	p.Ser458Ile(p.S458I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287169
Start	57692636:57692636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.686T>C
AA Mutation	p.Val229Ala(p.V229A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287169
Start	57696010:57696010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.976T>G
AA Mutation	p.Leu326Val(p.L326V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287169
Start	57696808:57696808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1057A>G
AA Mutation	p.Lys353Glu(p.K353E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287169
Start	57688585:57688585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.304C>T
AA Mutation	p.Arg102Cys(p.R102C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000287169
Start	57690420:57690420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.643C>T
AA Mutation	p.Arg215Cys(p.R215C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000287169
Start	57699048:57699048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775367827
CDS Mutation	c.1612C>T
AA Mutation	p.Arg538Cys(p.R538C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000287169
Start	57673151:57673151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777412510
CDS Mutation	c.61G>A
AA Mutation	p.Ala21Thr(p.A21T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287169
Start	57698633:57698633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1197G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287169
Start	57698690:57698690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555991599
CDS Mutation	c.1254C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000287169
Start	57699934:57699934(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2054delC
AA Mutation	p.Pro685LeufsTer68(p.P685Lfs*68)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000287169
Start	57688540:57688540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.259C>T
AA Mutation	p.Arg87Ter(p.R87*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZDHHC5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287169
Start	57698566:57698566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755434833
CDS Mutation	c.1130G>A
AA Mutation	p.Arg377His(p.R377H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000287169
Start	57682541:57682541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224G>A
AA Mutation	p.Arg75Gln(p.R75Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287169
Start	57693908:57693908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.878G>T
AA Mutation	p.Arg293Ile(p.R293I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript